Abstracts of the 39th Annual Meeting of the Society of Neuropediatrics

Abel, L

Mutation analysis of KCNAB1 in rolandic epilepsy

Abela, L

Fatal outcome of rhino-orbital-cerebral mucormycosis due to bilateral internal carotid occlusion in a child after hematopoietic stem cell transplantation

Abicht, A

A new heterozygote sequence variant of the CDKL5 Gene as the underlying cause of intractable early infantile epilepsy

Adler, C

Activities of daily living in children with hemiparesis: Influence of cognitive functions and motor competence on quality of performance

Outcome measurement in clinical pediatric neurorehabilitation: assessment of motor and process skills evaluates the effect of therapy in the area of activity of daily living

Ahlbory, K

Nicolaides-Baraitser Syndrome

Ahlenstiel, T

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Ahting, U

Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype

Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

The German network for mitochondrial disorders (mitoNET)

Aiello, C

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Alber, M

Early childhood onset progressive myoclonic epilepsy phenotype caused by KCTD7 mutations

Albers, J

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Albers, K

Jacobsen syndrome: a rare differential diagnosis of multifocal white matter lesions

Albrecht, B

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan

Tetrasomy X and neuropathy: double trouble or extended phenotype?

Albrecht, U

Visual disorders in children with cerebral palsy

Epilepsy in children with cerebral palsy

Arnold, C

Visual disorders in children with cerebral palsy

Asmussen, M

Jacobsen syndrome: a rare differential diagnosis of multifocal white matter lesions

Assmann, B

Atypical Infantile neuroaxonal dystrophy: a case report

Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene

Case report: cerebral atrophy-induced hygroma in a 3-month-old floppy infant: Unusual and severe manifestation of 5-methylentetrahydrofolate reductase (MTHFR) deficiency

Behçet disease – a rare differential diagnosis of inflammatory CNS disease in children

Au, K von

Ocular myasthenia with both AChR and MuSK antibodies

Auffermann, H

Which covariates influence effectiveness of intensified robotic-assisted treadmill therapy in children with cerebral palsy

Auvin, S

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Bächli, H

Postural headache due to spontaneous intracranial hypotension in an adolescent

Bader, P

Myoclonic epilepsy as affection of central nervous system in Farber disease

Badinger, A

Coincidence of duplication in the PCDH 19 gene and focal cortical dysplasia

Baethmann, M

Fatal outcome in a case of recurrent acute necrotizing encephalopathy with RANBP2 gene mutation: importance and difficulty of an early MRI pattern recognition

Lafora disease in a 17-year-old boy due to a compound heterozygous mutation in the NHLRC1 gene

Pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis in a 14-year-old girl probably associated with celiac disease

Confirmation of congenital mirror movements in a 19-month-old boy by detection of a de novo DCC mutation

Baldissera, I

Visual disorders in children with cerebral palsy

Intermittent eye motility disorder with elevation deficiency of one eye

Baltsavias, G

Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich

Bandowski, J

German-wide survey on the management of status epilepticus in children

Banwell, B

Plasma exchange in pediatric central nervous system inflammatory demyelination

Pediatric neuromyelitis optica-beyond the optic nerve and spinal cord

Bargehr, C

Neuropsychological long-term outcome in children with SVT

Bast, T

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Panic attacks in girls with double cortex syndrome: ictal amaurosis

A double-blinded, randomized, head-to-head trial of levetiracetam versus sulthiame in benign epilepsy with centrotemporal spikes

Impairment of synaptic downscaling: A potential mechanism for neuropsychological deficits in continuous spike waves during slow wave sleep

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Bauder, F

Primary central nervous system vasculitis in childhood: more frequent and variable than thought

Bauer, A

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Bauer, P

Specific pontine MRI-pattern is a helpful marker to recognize ataxia Charlevoix-Saguenay

Baumann, M

Status epilepticus caused by hypocalcaemia in a 6-month old child with hypoparathyroidism

Analysis of myogenic and endothelial progenitor cells in muscle biopsies of juvenile dermatomyositis

Epileptic seizures and chromosomal microdeletions/duplications

Familial occurrence of a 16p13 microdeletion including GRIN2A as a cause of developmental delay and epilepsy with continuous spike and waves during sleep

Epilepsy in children with cerebral palsy

Jeavon syndrome as a differential diagnosis of facial tics

Intermittent eye motility disorder with elevation deficiency of one eye

Baumgartner, B

Cardiomyopathy in a patient with Mb Duchenne first presenting as myocardial infarction in childhood

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Baumgartner, M

Methylenetetrahydrofolate reductase deficiency: therapy and outcome (with video)

Head nodding-differential diagnostic main sign

Myoclonus dystonia without dystonia

Baumgartner, S

Epilepsy in children with cerebral palsy

Jeavon syndrome as a differential diagnosis of facial tics

Baumgartner Sigl, S

Epileptic seizures and chromosomal microdeletions/duplications

Baumgartner-Sigl, S

Status epilepticus caused by hypocalcaemia in a 6-month old child with hypoparathyroidism

Baz Bartels, M

Myoclonic epilepsy as affection of central nervous system in Farber disease

Beck, H

A mutation in the SCN2A gene associated with BFNIS leads to seizures and behavioral impairment in a mouse model

Becker, J

Young adults with dyskinetic cerebral palsy improve subjectively on pallidal stimulation but not in formal dystonia, gait, speech, and swallowing testing

Becker, K

Neurodegeneration with brain iron accumulation type 4 by mutation in the C19orf12 gene: first time found in adolescent of Russian origin

Beier, J

Closure of meningomyeloceles with the 4-flap compound technique according to Ramirez

Benseler, S

Pediatric neuromyelitis optica-beyond the optic nerve and spinal cord

Berg, V

Heterozygous deletion of exon 3 of phospholipase C β1 gene causes neonatal epileptic encephalopathy?

Berger, T

A physiological characterization of biphasic transcranial magnetic stimulation

Bernert, G

Progressive myoclonus epilepsy: a differential diagnosis from juvenile chorea Huntington disease

Bernhard, MK

Ambulatory follow-up care of children treated with anticonvulsants and knowledge of parents regarding emergency treatment and safety precautions

Bernius, P

The Ulzibat method – a new surgical technique

Bertini, E

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Bertsche, A

Ambulatory follow-up care of children treated with anticonvulsants and knowledge of parents regarding emergency treatment and safety precautions

Bertsche, T

Ambulatory follow-up care of children treated with anticonvulsants and knowledge of parents regarding emergency treatment and safety precautions

Berweck, S

Which covariates influence effectiveness of intensified robotic-assisted treadmill therapy in children with cerebral palsy

Intraventricular baclofen therapy in refractory secondary dystonia-Indication, methodology, safety, and first results

Activities of daily living in children with hemiparesis: Influence of cognitive functions and motor competence on quality of performance

Severe dystonia caused by hemolytic-uremic syndrome with characteristic MRI scans

Interhemispheric connectivity in congenital hemiparesis

Outcome measurement in clinical pediatric neurorehabilitation: assessment of motor and process skills evaluates the effect of therapy in the area of activity of daily living

Biebl, A

Kernicterus: a case study

Transverse myelitis versus encephalitis disseminata

Steroids can influence the outcome of acute necroting encephalopathy

Congenital myasthenic syndromes: a difficult approach to diagnosis and therapy

Facial nerve palsy in children – is it as benign as supposed?

Bien, C

Anti-N-methyl-d-aspartate-receptor-encephalitis

Bien, CG

Central nervous system autoimmune syndrome associated with neuronal surface antibodies in the course of Enterovirus encephalitis

Uncommon presentation of voltage-gated potassium channel complex-antibody mediated central nervous system disease with eye movement disorder and ataxia

Bierhals, T

Confirmation of congenital mirror movements in a 19-month-old boy by detection of a de novo DCC mutation

Bigi, S

Plasma exchange in pediatric central nervous system inflammatory demyelination

Pediatric neuromyelitis optica-beyond the optic nerve and spinal cord

Bildstein, T

Epilepsy in children with cerebral palsy

Bimböse, P

Vitamin B in paediatric neurology

Bindt, C

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Biskup, S

Early childhood onset progressive myoclonic epilepsy phenotype caused by KCTD7 mutations

Paroxysmal dyskinesia due to PRRT2 mutation in 15-year-old female patient with benign familial infantile convulsions

Biotin-responsive basal ganglia disease in a 10-year-old German girl without SLC19A3 gene mutation

Mitochondrial encephalomyopathy presenting with deafness, mutism, ataxia and late onset external ophthalmoplegia caused by a mutation in the X-linked gene AIFM1

Biskup, W

Recurrent fever episodes after treatment of a subdural empyema: persisting infection or autoimmunological reaction?

Bittner, RE

Muscle-specific discordant skewing of X-chromosome inactivation leads to different clinical phenotypes of Duchenne muscular dystrophy in two monozygotic female twins

Blank, C

Dramatic neurological signs in children with intussusception

Blankenburg, M

Quantitative sensory testing in children and adolescents with tension type headache: changes in nociceptive processing are not specific for migraine

Biotin-responsive basal ganglia disease in a 10-year-old German girl without SLC19A3 gene mutation

Blaschek, A

Early white matter changes in childhood multiple sclerosis

Case report: oculomotor apraxia in ataxia telangiectasia

Blassnig-Ezeh, A

Benign partial epilepsy of infancy as defined by Watanabe: 2 case reports

Blau, N

Tetrahydrobiopterin deficiencies: an international survey of clinical and biochemical features, treatment strategies and follow-up of 626 patients

Bley, A

Hematopoietic stem cell transplantation (HSCT) in nine patients with juvenile MLD

Bluemcke, I

Coincidence of duplication in the PCDH 19 gene and focal cortical dysplasia

Boeckler, D

Hereditary neuralgic Amyotrophy – a case report of an affected family

Böhringer, E

Lafora disease in a 17-year-old boy due to a compound heterozygous mutation in the NHLRC1 gene

Characteristic MRI finding in severe tick-borne encephalitis in children and the effect of immunoglobulin G on the course of the disease

Böhringer, EM

Complex I and IV deficiency in an athletic adolescent with mild global retardation, exertional dyspnea, hypertrophic cardiomyopathy, and slight dysdiadochokinesia

Bok, L

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

Bölsterli Heinzle, B

Impairment of synaptic downscaling: A potential mechanism for neuropsychological deficits in continuous spike waves during slow wave sleep

Bolte, A

Nicolaides-Baraitser Syndrome

Boltshauser, E

Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum

Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

Congenital myopathy or neurofibromatosis type 1?

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Bonfert, M

A double-blinded, randomized, head-to-head trial of levetiracetam versus sulthiame in benign epilepsy with centrotemporal spikes

Bönnemann, C

Divergence in clinical presentation of Dynamin2-caused centronuclear myopathy is associated with mutations in distinct parts of the DNM2 gene

Borggraefe, I

Which covariates influence effectiveness of intensified robotic-assisted treadmill therapy in children with cerebral palsy

Borggräfe, I

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings

A double-blinded, randomized, head-to-head trial of levetiracetam versus sulthiame in benign epilepsy with centrotemporal spikes

Borusiak, P

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Bosemani, T

Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

Brackmann, F

Regenerative neuronal proliferation in hypoxic developing mouse brain is transient and modified by erythropoietin treatment

Interplay of inflammation and hypoxia in perinatal brain injury

Brockmann, K

Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism: Phenotypic spectrum of ATP1A3-associated disorders

Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders

Brückner, F

Isolated trochlear palsy in Lyme disease may persist

Brueckner, F

Paroxysmal dyskinesia due to PRRT2 mutation in 15-year-old female patient with benign familial infantile convulsions

13-year-old girl with antiphospholipid antibody-related chorea

Bruhn, H

Frontocerebellar tract lesions revealed by tractography in pediatric posterior fossa tumor survivors

Brunner, J

Lyme neuroborreliosis: aetiology and diagnosis of facial palsy in children from Tyrol

Brunner-Krainz, M

Vagal nerve stimulator in childhood absence epilepsy: 2 case reports

PANK2 disease with early onset: clinical and radiologic findings under short term treatment with deferiprone

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Antibodies against Mycoplasma pneumoniae in three patients with meningoencephalitis-causal relationship or epiphenomenon?

Tuberous sclerosis complex-successful therapy with everolimus

Autologous stem cell transplantation – a therapeutic option in childhood onset chronic inflammatory demyelinating polyneuroradiculopathy?

Bubl, BM

Complex I and IV deficiency in an athletic adolescent with mild global retardation, exertional dyspnea, hypertrophic cardiomyopathy, and slight dysdiadochokinesia

Buchfelder, M

Closure of meningomyeloceles with the 4-flap compound technique according to Ramirez

Büchner, B

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation

The German network for mitochondrial disorders (mitoNET)

Buck, A

Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich

Burfeind, P

Progressive myoclonus epilepsy: a differential diagnosis from juvenile chorea Huntington disease

Bürger, U

Characteristic MRI finding in severe tick-borne encephalitis in children and the effect of immunoglobulin G on the course of the disease

Bürki, S

Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

Busch, V

Central nervous system demyelination complicating Guillain-Barré syndrome

Busche, A

A large homozygous microdeletion in the RAB3GAP1 gene causes Warburg Micro syndrome

Bushby, K

Current care practice in Duchenne muscular dystrophy in Europe – results of the CARE-NMD cross-sectional survey

Büsscher, U

Isolated trochlear palsy in Lyme disease may persist

Bußmann, C

Postural headache due to spontaneous intracranial hypotension in an adolescent

Case report: cerebral atrophy-induced hygroma in a 3-month-old floppy infant: Unusual and severe manifestation of 5-methylentetrahydrofolate reductase (MTHFR) deficiency

Cag, C

Panic attacks in girls with double cortex syndrome: ictal amaurosis

Canstein, B

Outcome measurement in clinical pediatric neurorehabilitation: assessment of motor and process skills evaluates the effect of therapy in the area of activity of daily living

Capone Mori, A

Congenital myopathy or neurofibromatosis type 1?

Ceulemans, B

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Christen, HJ

Herpes simplex virus encephalitis – an unexpected relapse with choreoathetosis

Anti-N-methyl-d-aspartate-receptor encephalitis in a patient with acute organic brain syndrome with catatonia

Claeys, K

Central nervous system demyelination complicating Guillain-Barré syndrome

Clayton, P

PNPO mutations in patients with pyridoxine dependent epilepsy

Cloppenborg, T

Mutation p.Trp3X and mild phenotype of Becker muscular dystrophy

Connolly, M

PNPO mutations in patients with pyridoxine dependent epilepsy

Critelli, H

Impairment of synaptic downscaling: A potential mechanism for neuropsychological deficits in continuous spike waves during slow wave sleep

Cuno, S

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Dahse, AJ

Ambulatory follow-up care of children treated with anticonvulsants and knowledge of parents regarding emergency treatment and safety precautions

Das, A

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

Das, AM

Mutation p.Trp3X and mild phenotype of Becker muscular dystrophy

Datta, AN

Complex I and IV deficiency in an athletic adolescent with mild global retardation, exertional dyspnea, hypertrophic cardiomyopathy, and slight dysdiadochokinesia

Deanovic, D

Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich

Debus, O

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Deisenhammer, F

N-Methyl-D-Aspartate Receptor Antibodies in Neuroinflammatory Diseases

Deistung, A

Longitudinal Evaluation of Brain Iron Depositions in a Patient With Confirmed c19orf12 Mutation Using R2* Relaxometry and Quantitative Susceptibility Mapping

Dekomien, G

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt

Della Marina, A

Alpha-dystroglycanopathies: Clinical and genetic variability

Delvendahl, I

A physiological characterization of biphasic transcranial magnetic stimulation

der Hagen, M von

Hypertrophic olivary degeneration: a differential diagnosis to consider following surgical intervention in the posterior cranial fossa: review and two case reports

Mycoplasma pneumoniae and Borrelia burgdorferi as cause for facial paralysis in children: single-center experience of 10 years

Central nervous system autoimmune syndrome associated with neuronal surface antibodies in the course of Enterovirus encephalitis

Rituximab and Cyclophosphamide as an alternative in immunomodulatory therapy in Rasmussen encephalitis

Deschauer, M

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt

Deutz, U

Neurometabolic changes in patients with subacute sclerosing panencephalitis

Distelmaier, F

Transient ischemic attack in a 5-year-old girl due to focal vasculitis in neuroborreliosis

Recurrent fever episodes after treatment of a subdural empyema: persisting infection or autoimmunological reaction?

Biotin-responsive basal ganglia disease: a treatable differential diagnosis of Leigh syndrome

Dörr, HG

X-linked Creatine transport deficiency: Phenotypic variability in a family with SLC6A8 gene mutation

Doszpod, N

Case report: cerebral atrophy-induced hygroma in a 3-month-old floppy infant: Unusual and severe manifestation of 5-methylentetrahydrofolate reductase (MTHFR) deficiency

Dreha-Kulaczewski, S

Stepwise adaptation of treatment with calcium folinate in different modes of application leads to optimal therapeutic results for patients with cerebral folate transport deficiency

Drenckhahn, A

Ocular myasthenia with both AChR and MuSK antibodies

Dütemeyer, T

Case report: cerebral atrophy-induced hygroma in a 3-month-old floppy infant: Unusual and severe manifestation of 5-methylentetrahydrofolate reductase (MTHFR) deficiency

Dysek, S

Muscle-specific discordant skewing of X-chromosome inactivation leads to different clinical phenotypes of Duchenne muscular dystrophy in two monozygotic female twins

Eberhardt, H

Dramatic neurological signs in children with intussusception

Eder, H

Vagal nerve stimulator in childhood absence epilepsy: 2 case reports

Eisenkölbl, A

Kernicterus: a case study

Transverse myelitis versus encephalitis disseminata

Paroxysmal kinesogenic dyskinesia

13-year-old patient with headache, unclear on/off symptoms and psychosocial burden

Facial nerve palsy in children – is it as benign as supposed?

Ellenberger, D

Apheresis in the treatment of an acute attack of a demyelinating central nervous system disorder

Elpers, C

Rare cause of oculomotor palsy

Listening is all important!

Evolution of a channelopathy, CACNA1 mutation in a young man

Ketogenic diet in children with pharmacoresistant epilepsy

Kleine-Levin syndrome in a 10-year-old boy as the rare cause of hypersomnia

Fibroadenoma under therapy with interferons in multiple sclerosis

Endele, S

Nicolaides-Baraitser Syndrome

Engeland, B

A mutation in the SCN2A gene associated with BFNIS leads to seizures and behavioral impairment in a mouse model

Ensslen, M

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings

Ertl-Wagner, B

Early white matter changes in childhood multiple sclerosis

Eyüpoglu, I

Ultrasound-guided neuronavigation-the safest approach for Rickham capsule insertion in preterm infants

Eyüpoglu, IY

Closure of meningomyeloceles with the 4-flap compound technique according to Ramirez

Fauth, C

Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum

Epileptic seizures and chromosomal microdeletions/duplications

Familial occurrence of a 16p13 microdeletion including GRIN2A as a cause of developmental delay and epilepsy with continuous spike and waves during sleep

Fazeli, W

A mutation in the SCN2A gene associated with BFNIS leads to seizures and behavioral impairment in a mouse model

Feige, B

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Fiedler, A

A new heterozygote sequence variant of the CDKL5 Gene as the underlying cause of intractable early infantile epilepsy

Treatment of therapy-resistant sialorrhea with transdermal scopolamine in a 10-year-old girl with Wolf-Hirschhorn syndrome

Fiedler, B

Rare cause of oculomotor palsy

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Lacosamide in childhood-results of a retrospective analysis

Listening is all important!

Ocular myositis

Evolution of a channelopathy, CACNA1 mutation in a young man

Vitamin B in paediatric neurology

Ketogenic diet in children with pharmacoresistant epilepsy

Kleine-Levin syndrome in a 10-year-old boy as the rare cause of hypersomnia

Fibroadenoma under therapy with interferons in multiple sclerosis

Fink, GR

Young adults with dyskinetic cerebral palsy improve subjectively on pallidal stimulation but not in formal dystonia, gait, speech, and swallowing testing

Fischer, D

Congenital myopathy or neurofibromatosis type 1?

Flores-Sarnat, L

Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

Flossdorf, P

Young adults with dyskinetic cerebral palsy improve subjectively on pallidal stimulation but not in formal dystonia, gait, speech, and swallowing testing

Fogarasi, A

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Franck, EM

Anti-N-methyl-d-aspartate-receptor encephalitis in a patient with acute organic brain syndrome with catatonia

Franke, K

Increasing prematurity is associated with a more pronounced delay in brain maturation in older children and adolescents

Freilinger, M

Muscle-specific discordant skewing of X-chromosome inactivation leads to different clinical phenotypes of Duchenne muscular dystrophy in two monozygotic female twins

Quality of life and mental health of neuropediatric patients

Atypical and mild clinical manifestation in a boy with mitochondrial ATP6 mutation

Freisinger, P

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype

Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

The German network for mitochondrial disorders (mitoNET)

Freudenberg, L

Hypertrophic olivary degeneration: a differential diagnosis to consider following surgical intervention in the posterior cranial fossa: review and two case reports

Frey, D

Interplay of inflammation and hypoxia in perinatal brain injury

Fricke, O

Young adults with dyskinetic cerebral palsy improve subjectively on pallidal stimulation but not in formal dystonia, gait, speech, and swallowing testing

Friebel, D

Rituximab and Cyclophosphamide as an alternative in immunomodulatory therapy in Rasmussen encephalitis

Friede, T

Apheresis in the treatment of an acute attack of a demyelinating central nervous system disorder

Froelich, S

Natural course of pontocerebellar hypoplasia Type 2

Frontini, R

Ambulatory follow-up care of children treated with anticonvulsants and knowledge of parents regarding emergency treatment and safety precautions

Frühwald, MC

Uncommon presentation of voltage-gated potassium channel complex-antibody mediated central nervous system disease with eye movement disorder and ataxia

Furthner, D

Cerebral seizures, cardiopulmonary resuscitation, and posterior reversible encephalopathy syndrome after accidental ingestion of xylocain gel 2%

Congenital myasthenic syndromes: a difficult approach to diagnosis and therapy

Facial nerve palsy in children – is it as benign as supposed?

Fussenegger, B

Predictors of academic difficulties in preterm children compared with term-born children at the age of 5 years

Gädeke, JC

Intra- and cross-modal refractory period effects in healthy children and adults: An ERP study

Gallistl, S

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Ganslandt, O

Closure of meningomyeloceles with the 4-flap compound technique according to Ramirez

Ultrasound-guided neuronavigation-the safest approach for Rickham capsule insertion in preterm infants

Garavaglia, B

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation

Garkisch, S

Mutation analysis of KCNAB1 in rolandic epilepsy

Gärtner, J

Autosomal-recessive Kearns-Sayre syndrome is caused by mutations in the RRM2B gene with altered mitochondrial transcription

Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism: Phenotypic spectrum of ATP1A3-associated disorders

Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders

Evidence against the concept of chronic cerebrospinal venous insufficiency in multiple sclerosis

Disequilibrium syndrome caused by an unusual constellation of VLDLR mutations

Stepwise adaptation of treatment with calcium folinate in different modes of application leads to optimal therapeutic results for patients with cerebral folate transport deficiency

Apheresis in the treatment of an acute attack of a demyelinating central nervous system disorder

Mitochondrial encephalomyopathy presenting with deafness, mutism, ataxia and late onset external ophthalmoplegia caused by a mutation in the X-linked gene AIFM1

Gaser, C

Increasing prematurity is associated with a more pronounced delay in brain maturation in older children and adolescents

Gassner, S

Paroxysmal dyskinesia due to PRRT2 mutation in 15-year-old female patient with benign familial infantile convulsions

Gattinger, N

A physiological characterization of biphasic transcranial magnetic stimulation

Induction of cortical plasticity by biphasic quadro-pulse stimulation

Gautsch, K

Epileptic seizures and chromosomal microdeletions/duplications

Gburek-Augustat, J

Specific pontine MRI-pattern is a helpful marker to recognize ataxia Charlevoix-Saguenay

Gedik, A

Visual disorders in children with cerebral palsy

Epilepsy in children with cerebral palsy

Geis, T

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan

Giagkou, E

Neurodegeneration with brain iron accumulation type 4 by mutation in the C19orf12 gene: first time found in adolescent of Russian origin

Giner, T

Status epilepticus caused by hypocalcaemia in a 6-month old child with hypoparathyroidism

Gleich, B

A physiological characterization of biphasic transcranial magnetic stimulation

Induction of cortical plasticity by biphasic quadro-pulse stimulation

Goebel, HH

Molecular mechanisms of juvenile dermatomyositis

Goelz, R

Increasing prematurity is associated with a more pronounced delay in brain maturation in older children and adolescents

Gold, R

A prospective study on 71 children to investigate normative pediatric values in optical coherence tomography

Visual impairment – differential diagnoses

Göpel, W

Do developmental problems perceived by parents of very-low-birth weight infants during the first year of life correlate with objective criteria at 2 years of age?

Gosk, M

Progressive myoclonus epilepsy: a differential diagnosis from juvenile chorea Huntington disease

Gospe, S

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

Gramsch, K

Current care practice in Duchenne muscular dystrophy in Europe – results of the CARE-NMD cross-sectional survey

Granel, M

Intraventricular baclofen therapy in refractory secondary dystonia-Indication, methodology, safety, and first results

Severe dystonia caused by hemolytic-uremic syndrome with characteristic MRI scans

Grasl, C

Guidelines and examples for orthotic treatment of children and youth in case of myelomeningocele

Gröschel, S

Loss of speech in late-infantile and juvenile metachromatic leukodystrophy

Grosse, R

Longitudinal Evaluation of Brain Iron Depositions in a Patient With Confirmed c19orf12 Mutation Using R2* Relaxometry and Quantitative Susceptibility Mapping

Gruber-Sedlmayr, U

Vagal nerve stimulator in childhood absence epilepsy: 2 case reports

PANK2 disease with early onset: clinical and radiologic findings under short term treatment with deferiprone

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Antibodies against Mycoplasma pneumoniae in three patients with meningoencephalitis-causal relationship or epiphenomenon?

Tuberous sclerosis complex-successful therapy with everolimus

Autologous stem cell transplantation – a therapeutic option in childhood onset chronic inflammatory demyelinating polyneuroradiculopathy?

Grulich-Henn, J

Behçet disease – a rare differential diagnosis of inflammatory CNS disease in children

Grummel, V

Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease

Guerrini, R

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Gumpold, C

Analysis of myogenic and endothelial progenitor cells in muscle biopsies of juvenile dermatomyositis

Güngör, T

Fatal outcome of rhino-orbital-cerebral mucormycosis due to bilateral internal carotid occlusion in a child after hematopoietic stem cell transplantation

Haack, T

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype

Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

Haack, TB

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature

Haas-Lude, K

Lambdoid synostosis or positional plagiocephaly – a visual diagnosis?

Haberberger, B

Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

Haberlandt, E

Status epilepticus caused by hypocalcaemia in a 6-month old child with hypoparathyroidism

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings

Epileptic seizures and chromosomal microdeletions/duplications

Familial occurrence of a 16p13 microdeletion including GRIN2A as a cause of developmental delay and epilepsy with continuous spike and waves during sleep

Benign partial epilepsy of infancy as defined by Watanabe: 2 case reports

Epilepsy in children with cerebral palsy

Jeavon syndrome as a differential diagnosis of facial tics

Hackenberg, A

Differential diagnosis of central nervous system vasculopathies: two case reports

Infantile choreatic movements, early onset severe epileptic encephalopathy, and primary developmental impairment as a result of a de novo missense mutation in the SCN2A gene

Fatal outcome of rhino-orbital-cerebral mucormycosis due to bilateral internal carotid occlusion in a child after hematopoietic stem cell transplantation

Hader, WJ

Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum

Haffner, D

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Hagel, C

Lafora disease in a 17-year-old boy due to a compound heterozygous mutation in the NHLRC1 gene

Hahn, A

Quantification of muscular morphological alterations in patients with infantile and early-juvenile Pompe disease

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Linear scleroderma en coup de sabre – two case reports with inflammatory CNS lesions

Hahn, G

Hypertrophic olivary degeneration: a differential diagnosis to consider following surgical intervention in the posterior cranial fossa: review and two case reports

Central nervous system autoimmune syndrome associated with neuronal surface antibodies in the course of Enterovirus encephalitis

Rituximab and Cyclophosphamide as an alternative in immunomodulatory therapy in Rasmussen encephalitis

Haidenthaler, P

13-year-old patient with headache, unclear on/off symptoms and psychosocial burden

Harms, N

Severe dystonia caused by hemolytic-uremic syndrome with characteristic MRI scans

Hartig, M

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Longitudinal Evaluation of Brain Iron Depositions in a Patient With Confirmed c19orf12 Mutation Using R2* Relaxometry and Quantitative Susceptibility Mapping

Hartlieb, T

Intraventricular baclofen therapy in refractory secondary dystonia-Indication, methodology, safety, and first results

Hartman, AL

Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

Hartmann, B

Disequilibrium syndrome caused by an unusual constellation of VLDLR mutations

A large homozygous microdeletion in the RAB3GAP1 gene causes Warburg Micro syndrome

Hartmann, H

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Mutation p.Trp3X and mild phenotype of Becker muscular dystrophy

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

Hartmann, M

Hematopoietic stem cell transplantation (HSCT) in nine patients with juvenile MLD

Hasselmann, O

PNPO mutations in patients with pyridoxine dependent epilepsy

Hassink, R

Dopamine-responsive dystonia: Clinical and therapeutic variability with identical genetic defect

Haug, C

Induction of cortical plasticity by biphasic quadro-pulse stimulation

Haug, V

Complex regional pain syndrome I following vaccination against human papillomavirus

Hauke, K

Complex regional pain syndrome I following vaccination against human papillomavirus

Hauser, TK

Increasing prematurity is associated with a more pronounced delay in brain maturation in older children and adolescents

Häusler, M

Central nervous system demyelination complicating Guillain-Barré syndrome

Neurometabolic changes in patients with subacute sclerosing panencephalitis

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Hayflick, S

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Hedrich, U

A mutation in the SCN2A gene associated with BFNIS leads to seizures and behavioral impairment in a mouse model

Hehr, U

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan

Alpha-dystroglycanopathies: Clinical and genetic variability

Heider, C

Ischemic Stroke in a 14-year-old Boy with Homozygous C677T MTHFR Mutation

Heimering, S

A new heterozygote sequence variant of the CDKL5 Gene as the underlying cause of intractable early infantile epilepsy

Treatment of therapy-resistant sialorrhea with transdermal scopolamine in a 10-year-old girl with Wolf-Hirschhorn syndrome

Heinen, F

Which covariates influence effectiveness of intensified robotic-assisted treadmill therapy in children with cerebral palsy

Early white matter changes in childhood multiple sclerosis

Interhemispheric connectivity in congenital hemiparesis

A double-blinded, randomized, head-to-head trial of levetiracetam versus sulthiame in benign epilepsy with centrotemporal spikes

Heinrich, B

Unusual prodromal manifestation of neuromyelitis optica with prolonged seizures, fever, CSF pleocytosis and encephalopathic EEG-pattern

Heinzle, J

Impairment of synaptic downscaling: A potential mechanism for neuropsychological deficits in continuous spike waves during slow wave sleep

Hemmer, B

Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease

Hempel, M

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature

Henkes, H

Rare cause of oculomotor palsy

Herkenrath, P

Lacosamide in childhood-results of a retrospective analysis

Hernaiz-Driever, P

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Hernáiz Driever, P

Frontocerebellar tract lesions revealed by tractography in pediatric posterior fossa tumor survivors

Herterich, R

Cardiomyopathy in a patient with Mb Duchenne first presenting as myocardial infarction in childhood

Dramatic neurological signs in children with intussusception

Herting, E

Do developmental problems perceived by parents of very-low-birth weight infants during the first year of life correlate with objective criteria at 2 years of age?

Hertzberg, C

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Heruth, M

Hereditary neuralgic Amyotrophy – a case report of an affected family

Herzog, A

Hereditary congenital mirror movements

Hessenauer, M

Outcome measurement in clinical pediatric neurorehabilitation: assessment of motor and process skills evaluates the effect of therapy in the area of activity of daily living

Hethey, S

Lacosamide in childhood-results of a retrospective analysis

Herpes simplex virus encephalitis – an unexpected relapse with choreoathetosis

Anti-N-methyl-d-aspartate-receptor encephalitis in a patient with acute organic brain syndrome with catatonia

Heußinger, N

Ultrasound-guided neuronavigation-the safest approach for Rickham capsule insertion in preterm infants

X-linked Creatine transport deficiency: Phenotypic variability in a family with SLC6A8 gene mutation

Heyer, C

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt

Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene

Hiener, U

Fatal outcome in a case of recurrent acute necrotizing encephalopathy with RANBP2 gene mutation: importance and difficulty of an early MRI pattern recognition

Hillebrand, M

Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders

Hillebrandt, G

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Hinderhofer, K

Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene

Hirsch, A

Closure of meningomyeloceles with the 4-flap compound technique according to Ramirez

Hirschfeld, G

Quantitative sensory testing in children and adolescents with tension type headache: changes in nociceptive processing are not specific for migraine

Hjalgrim, H

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Hobbiebrunken, E

Divergence in clinical presentation of Dynamin2-caused centronuclear myopathy is associated with mutations in distinct parts of the DNM2 gene

Hoelzle, M

Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich

Hoess, C

Induction of cortical plasticity by biphasic quadro-pulse stimulation

Hofer, D

PNPO mutations in patients with pyridoxine dependent epilepsy

Hoffmann, GF

Neurometabolic changes in patients with subacute sclerosing panencephalitis

Tetrahydrobiopterin deficiencies: an international survey of clinical and biochemical features, treatment strategies and follow-up of 626 patients

Hofmann, C

Complex regional pain syndrome I following vaccination against human papillomavirus

Hofmann, R

Linear scleroderma en coup de sabre – two case reports with inflammatory CNS lesions

Holert, N

Rituximab and Cyclophosphamide as an alternative in immunomodulatory therapy in Rasmussen encephalitis

Holinksi-Feder, E

Coincidence of duplication in the PCDH 19 gene and focal cortical dysplasia

Holinski-Feder, E

Hereditary neuralgic Amyotrophy – a case report of an affected family

Holthausen, H

Coincidence of duplication in the PCDH 19 gene and focal cortical dysplasia

Holz, J

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Homburg, M

Which covariates influence effectiveness of intensified robotic-assisted treadmill therapy in children with cerebral palsy

Honold, M

Visual disorders in children with cerebral palsy

Horch, RE

Closure of meningomyeloceles with the 4-flap compound technique according to Ramirez

Horgath, P

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Horn, D

A large homozygous microdeletion in the RAB3GAP1 gene causes Warburg Micro syndrome

Horstmann, D

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Horvath, R

Autosomal-recessive Kearns-Sayre syndrome is caused by mutations in the RRM2B gene with altered mitochondrial transcription

Hosie, S

Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease

Hotz, A

Disequilibrium syndrome caused by an unusual constellation of VLDLR mutations

Hroncek, K

Facial nerve palsy in children – is it as benign as supposed?

Huber, R

Impairment of synaptic downscaling: A potential mechanism for neuropsychological deficits in continuous spike waves during slow wave sleep

Huemer, C

Neurological symptoms and demyelinating changes on MRI at 3 brothers with cryopyrin-associated periodic syndrome

Hug, M

Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich

Huhle, D

Hereditary neuralgic Amyotrophy – a case report of an affected family

Huisman, TAGM

Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum

Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

Maturation of the brainstem and cerebellar white matter tracts from the neonatal period to adolescence: a diffusion tensor imaging study

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Hummel, HM

Evidence against the concept of chronic cerebrospinal venous insufficiency in multiple sclerosis

Huppke, B

Apheresis in the treatment of an acute attack of a demyelinating central nervous system disorder

Huppke, P

Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism: Phenotypic spectrum of ATP1A3-associated disorders

Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders

Apheresis in the treatment of an acute attack of a demyelinating central nervous system disorder

Mitochondrial encephalomyopathy presenting with deafness, mutism, ataxia and late onset external ophthalmoplegia caused by a mutation in the X-linked gene AIFM1

Biotin-responsive basal ganglia disease: a treatable differential diagnosis of Leigh syndrome

Iff, T

Unusual prodromal manifestation of neuromyelitis optica with prolonged seizures, fever, CSF pleocytosis and encephalopathic EEG-pattern

Irnich, B

Acute hemiataxia in childhood

Isbrandt, D

A mutation in the SCN2A gene associated with BFNIS leads to seizures and behavioral impairment in a mouse model

Issa, L

Effects of CDK5RAP2 downregulation in murine embryonic stem cells correlate with cellular phenotype in MCPH3 patients

Jacobs, E

Mycoplasma pneumoniae and Borrelia burgdorferi as cause for facial paralysis in children: single-center experience of 10 years

Jaggumantri, S

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

Jahn, K

Which covariates influence effectiveness of intensified robotic-assisted treadmill therapy in children with cerebral palsy

Case report: oculomotor apraxia in ataxia telangiectasia

Jakobs, C

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

Janetschek, C

Epileptic seizures and chromosomal microdeletions/duplications

Epilepsy in children with cerebral palsy

Janzen, N

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt

Methylenetetrahydrofolate reductase deficiency: therapy and outcome (with video)

Jarisch, A

Myoclonic epilepsy as affection of central nervous system in Farber disease

Jenni, OG

Impairment of synaptic downscaling: A potential mechanism for neuropsychological deficits in continuous spike waves during slow wave sleep

Johannes, M

Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype

Johannsen, J

Intra- and cross-modal refractory period effects in healthy children and adults: An ERP study

Juenger, H

Interhemispheric connectivity in congenital hemiparesis

Jung, C

Jacobsen syndrome: a rare differential diagnosis of multifocal white matter lesions

Jung, N

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Induction of cortical plasticity by biphasic quadro-pulse stimulation

Jung, S

Regenerative neuronal proliferation in hypoxic developing mouse brain is transient and modified by erythropoietin treatment

Interplay of inflammation and hypoxia in perinatal brain injury

Jüngert, J

Ultrasound-guided neuronavigation-the safest approach for Rickham capsule insertion in preterm infants

Kadish Navah, E

Implementation of a (neuro-)psychological screening of infants with newly diagnosed epilepsy. Practicability and first results concerning potential premorbid problems

Kager, K

Predictors of academic difficulties in preterm children compared with term-born children at the age of 5 years

Kaindl, A

A large homozygous microdeletion in the RAB3GAP1 gene causes Warburg Micro syndrome

Effects of CDK5RAP2 downregulation in murine embryonic stem cells correlate with cellular phenotype in MCPH3 patients

Kaindl, AM

Ocular myasthenia with both AChR and MuSK antibodies

Kalle, T von

Biotin-responsive basal ganglia disease in a 10-year-old German girl without SLC19A3 gene mutation

Kalluri, SR

Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease

Kana, V

Congenital myopathy or neurofibromatosis type 1?

Kang, KS

Atypical Infantile neuroaxonal dystrophy: a case report

Postural headache due to spontaneous intracranial hypotension in an adolescent

Case report: cerebral atrophy-induced hygroma in a 3-month-old floppy infant: Unusual and severe manifestation of 5-methylentetrahydrofolate reductase (MTHFR) deficiency

Kanz, S

PNPO mutations in patients with pyridoxine dependent epilepsy

Kapelari, K

Status epilepticus caused by hypocalcaemia in a 6-month old child with hypoparathyroidism

Karacevic-Preradovic, T

Lacosamide in childhood-results of a retrospective analysis

Karall, D

Epileptic seizures and chromosomal microdeletions/duplications

Karenfort, M

Transient ischemic attack in a 5-year-old girl due to focal vasculitis in neuroborreliosis

Biotin-responsive basal ganglia disease: a treatable differential diagnosis of Leigh syndrome

Karlmeier, A

Coincidence of duplication in the PCDH 19 gene and focal cortical dysplasia

Keeser, D

Early white matter changes in childhood multiple sclerosis

Kehrer, C

Loss of speech in late-infantile and juvenile metachromatic leukodystrophy

Keimer, R

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Keller, E

First experiences with fingolimod in two female adolescents with relapsing multiple sclerosis

Kemper, M

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Kettwig, M

Mitochondrial encephalomyopathy presenting with deafness, mutism, ataxia and late onset external ophthalmoplegia caused by a mutation in the X-linked gene AIFM1

Khan, N

Differential diagnosis of central nervous system vasculopathies: two case reports

Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich

Kiechl-Kohlendorfer, U

Predictors of academic difficulties in preterm children compared with term-born children at the age of 5 years

Kieslich, M

Atypical case of a neurocutaneous melanosis with typical magnetic resonance imaging findings

Myoclonic epilepsy as affection of central nervous system in Farber disease

Absent biochemical evidence at an early age delayed diagnosis in a patient with a clinically severe form of peroxisomal biogenesis disorder

Kiess, W

Ambulatory follow-up care of children treated with anticonvulsants and knowledge of parents regarding emergency treatment and safety precautions

Kirschner, J

Current care practice in Duchenne muscular dystrophy in Europe – results of the CARE-NMD cross-sectional survey

Klaus, K

Quality of life and mental health of neuropediatric patients

Klein, A

Differential diagnosis of central nervous system vasculopathies: two case reports

Congenital myopathy or neurofibromatosis type 1?

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Kleinlein, B

Fatal outcome in a case of recurrent acute necrotizing encephalopathy with RANBP2 gene mutation: importance and difficulty of an early MRI pattern recognition

Kleiter, I

Visual impairment – differential diagnoses

Klepper, J

Hereditary congenital mirror movements

Klinge, L

Mitochondrial encephalomyopathy presenting with deafness, mutism, ataxia and late onset external ophthalmoplegia caused by a mutation in the X-linked gene AIFM1

Klopstock, T

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation

The German network for mitochondrial disorders (mitoNET)

Kluger, G

Refractory epilepsy in a patient with Doose syndrome: favorable response after add-on therapy with bromide

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Severe dystonia caused by hemolytic-uremic syndrome with characteristic MRI scans

Lafora disease in a 17-year-old boy due to a compound heterozygous mutation in the NHLRC1 gene

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Characteristic MRI finding in severe tick-borne encephalitis in children and the effect of immunoglobulin G on the course of the disease

Different courses of Foix-Chavany-Marie syndrome (FCMS) in children with herpes encephalitis

Kmiec, T

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation

Kneser, U

Closure of meningomyeloceles with the 4-flap compound technique according to Ramirez

Knotz, J

Atypical case of a neurocutaneous melanosis with typical magnetic resonance imaging findings

Koch, J

Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Atypical and mild clinical manifestation in a boy with mitochondrial ATP6 mutation

Koerte, IK

Early white matter changes in childhood multiple sclerosis

Interhemispheric connectivity in congenital hemiparesis

Kohl, B

Paroxysmal dyskinesia due to PRRT2 mutation in 15-year-old female patient with benign familial infantile convulsions

13-year-old girl with antiphospholipid antibody-related chorea

Köhler, C

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt

Methylenetetrahydrofolate reductase deficiency: therapy and outcome (with video)

Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene

Visual impairment – differential diagnoses

Kohlhase, J

Biotin-responsive basal ganglia disease: a treatable differential diagnosis of Leigh syndrome

Kohlschütter, A

Lafora disease in a 17-year-old boy due to a compound heterozygous mutation in the NHLRC1 gene

Hematopoietic stem cell transplantation (HSCT) in nine patients with juvenile MLD

Longitudinal Evaluation of Brain Iron Depositions in a Patient With Confirmed c19orf12 Mutation Using R2* Relaxometry and Quantitative Susceptibility Mapping

Kohns, M

Transient ischemic attack in a 5-year-old girl due to focal vasculitis in neuroborreliosis

Kolb, AK

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Kölker, S

Methylenetetrahydrofolate reductase deficiency: therapy and outcome (with video)

Case report: cerebral atrophy-induced hygroma in a 3-month-old floppy infant: Unusual and severe manifestation of 5-methylentetrahydrofolate reductase (MTHFR) deficiency

Kolodzieczyk, D

Coincidence of duplication in the PCDH 19 gene and focal cortical dysplasia

Kommer, N

Biomechanical significance of the rotational axes in the orthotic care

Konzett, K

Pyridoxine-dependent epilepsy: case report

Kopajtich, R

Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype

Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

Korenke, C

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Heterozygous deletion of exon 3 of phospholipase C β1 gene causes neonatal epileptic encephalopathy?

Connatal brain hemorrhage as fetal manifestation of Osler-Weber-Rendu syndrome (hereditary hemorrhagic telangiectasia)

Anti-N-methyl-d-aspartate-receptor-encephalitis

Korinthenberg, R

Diagnostics and management of pediatric headaches at a University Hospital

Bone health and vitamin D metabolism in children and adolescents with Duchenne muscular dystrophy compared with other neuromuscular diseases and cerebral palsy

Kortschak, A

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Autologous stem cell transplantation – a therapeutic option in childhood onset chronic inflammatory demyelinating polyneuroradiculopathy?

Kotzot, D

Epileptic seizures and chromosomal microdeletions/duplications

Familial occurrence of a 16p13 microdeletion including GRIN2A as a cause of developmental delay and epilepsy with continuous spike and waves during sleep

Kovacevic-Preradovic, T

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Kowald, T

Connatal brain hemorrhage as fetal manifestation of Osler-Weber-Rendu syndrome (hereditary hemorrhagic telangiectasia)

Koy, A

Young adults with dyskinetic cerebral palsy improve subjectively on pallidal stimulation but not in formal dystonia, gait, speech, and swallowing testing

Koziolek, M

Apheresis in the treatment of an acute attack of a demyelinating central nervous system disorder

Krabichler, B

Familial occurrence of a 16p13 microdeletion including GRIN2A as a cause of developmental delay and epilepsy with continuous spike and waves during sleep

Krägeloh-Mann, I

Natural course of pontocerebellar hypoplasia Type 2

Early childhood onset progressive myoclonic epilepsy phenotype caused by KCTD7 mutations

Loss of speech in late-infantile and juvenile metachromatic leukodystrophy

Krämer, N

Effects of CDK5RAP2 downregulation in murine embryonic stem cells correlate with cellular phenotype in MCPH3 patients

Kraus, V

Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease

Krebs, A

Results of calcaneo stop arthroereisis in children with neuromotoric disorders

Kremens-Korsch, U

Nicolaides-Baraitser Syndrome

Kress, W

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan

Alpha-dystroglycanopathies: Clinical and genetic variability

Krimmel, M

Lambdoid synostosis or positional plagiocephaly – a visual diagnosis?

Kröll, J

Infantile choreatic movements, early onset severe epileptic encephalopathy, and primary developmental impairment as a result of a de novo missense mutation in the SCN2A gene

Kröpl, M

Steroids can influence the outcome of acute necroting encephalopathy

Kudernatsch, M

Coincidence of duplication in the PCDH 19 gene and focal cortical dysplasia

Intraventricular baclofen therapy in refractory secondary dystonia-Indication, methodology, safety, and first results

Stereo-EEG in children with therapy-refractory epilepsies: Robot-assistance plus stereotaxy combines speed with maximal precision for the implantation of multiple depth electrodes

Kufner, S

Confirmation of congenital mirror movements in a 19-month-old boy by detection of a de novo DCC mutation

Kühle, HJ

Video-assisted behavior observation as a tool for methylphenidate dose finding in ADHD: longer term outcome

Kunz, F

Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich

Küpper, H

Intraventricular baclofen therapy in refractory secondary dystonia-Indication, methodology, safety, and first results

Kurlemann, G

Rare cause of oculomotor palsy

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Lacosamide in childhood-results of a retrospective analysis

Listening is all important!

Ocular myositis

Evolution of a channelopathy, CACNA1 mutation in a young man

Vitamin B in paediatric neurology

Ketogenic diet in children with pharmacoresistant epilepsy

Kleine-Levin syndrome in a 10-year-old boy as the rare cause of hypersomnia

Fibroadenoma under therapy with interferons in multiple sclerosis

Kurver, A

Implementation of a (neuro-)psychological screening of infants with newly diagnosed epilepsy. Practicability and first results concerning potential premorbid problems

Kutsche, K

Confirmation of congenital mirror movements in a 19-month-old boy by detection of a de novo DCC mutation

Laccone, F

Progressive myoclonus epilepsy: a differential diagnosis from juvenile chorea Huntington disease

Laimbacher, J

Atypical Absences, developmental delay, and neonatal diabetes-think of DEND-Syndrome. A Channelopathy involving pancreas, muscle, and brain with possible improvement by sulfonylurea treatment

Langer, S

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Langhagen, T

Case report: oculomotor apraxia in ataxia telangiectasia

Lanzersdorfer, R

Ischemic Stroke in a 14-year-old Boy with Homozygous C677T MTHFR Mutation

Latal, B

Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich

Lauffer, H

Sturge-Weber syndrome with hyposomatotropism

Laws, HJ

Transient ischemic attack in a 5-year-old girl due to focal vasculitis in neuroborreliosis

Lechner, E

Facial nerve palsy in children – is it as benign as supposed?

Lefering, R

Video-assisted behavior observation as a tool for methylphenidate dose finding in ADHD: longer term outcome

Lehnhardt, A

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Leiz, S

Fatal outcome in a case of recurrent acute necrotizing encephalopathy with RANBP2 gene mutation: importance and difficulty of an early MRI pattern recognition

Lafora disease in a 17-year-old boy due to a compound heterozygous mutation in the NHLRC1 gene

Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis in a 14-year-old girl probably associated with celiac disease

Confirmation of congenital mirror movements in a 19-month-old boy by detection of a de novo DCC mutation

Lemke, J

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Lengnick, K

MLC-1-related megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap Disease) – a rare cause of macrocephaly and mild motor developmental delay

Lerche, H

A mutation in the SCN2A gene associated with BFNIS leads to seizures and behavioral impairment in a mouse model

Liao, Y

A mutation in the SCN2A gene associated with BFNIS leads to seizures and behavioral impairment in a mouse model

Liebig, T

Young adults with dyskinetic cerebral palsy improve subjectively on pallidal stimulation but not in formal dystonia, gait, speech, and swallowing testing

Linden, T

Listening is all important!

Evolution of a channelopathy, CACNA1 mutation in a young man

Ketogenic diet in children with pharmacoresistant epilepsy

Kleine-Levin syndrome in a 10-year-old boy as the rare cause of hypersomnia

Fibroadenoma under therapy with interferons in multiple sclerosis

Linder-Lucht, M

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Liu, Y

A mutation in the SCN2A gene associated with BFNIS leads to seizures and behavioral impairment in a mouse model

Löbel, U

Hematopoietic stem cell transplantation (HSCT) in nine patients with juvenile MLD

Longitudinal Evaluation of Brain Iron Depositions in a Patient With Confirmed c19orf12 Mutation Using R2* Relaxometry and Quantitative Susceptibility Mapping

Lochmüller, H

Current care practice in Duchenne muscular dystrophy in Europe – results of the CARE-NMD cross-sectional survey

Loddenkemper, T

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Loew, YM

Case report: cerebral atrophy-induced hygroma in a 3-month-old floppy infant: Unusual and severe manifestation of 5-methylentetrahydrofolate reductase (MTHFR) deficiency

Lohmann, E

Paroxysmal dyskinesia due to PRRT2 mutation in 15-year-old female patient with benign familial infantile convulsions

Lohse, P

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt

Loos, S

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Lotte, J

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Different courses of Foix-Chavany-Marie syndrome (FCMS) in children with herpes encephalitis

Lücke, T

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt

Methylenetetrahydrofolate reductase deficiency: therapy and outcome (with video)

A prospective study on 71 children to investigate normative pediatric values in optical coherence tomography

Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene

Stepwise adaptation of treatment with calcium folinate in different modes of application leads to optimal therapeutic results for patients with cerebral folate transport deficiency

Visual impairment – differential diagnoses

Luebbig, A

Coincidence of duplication in the PCDH 19 gene and focal cortical dysplasia

Lueck, C

Mycoplasma pneumoniae and Borrelia burgdorferi as cause for facial paralysis in children: single-center experience of 10 years

Lusch, E

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Lüsebrink, N

Absent biochemical evidence at an early age delayed diagnosis in a patient with a clinically severe form of peroxisomal biogenesis disorder

Lütschg, J

Benign partial epilepsy of infancy as defined by Watanabe: 2 case reports

Pyridoxine-dependent epilepsy: case report

Weakness of the limb girdle type with finger tremor and elevated creatine kinase

Lütschgg, J

Dopamine-responsive dystonia: Clinical and therapeutic variability with identical genetic defect

Lutz, S

Alpha-dystroglycanopathies: Clinical and genetic variability

Tetrasomy X and neuropathy: double trouble or extended phenotype?

Neurodegeneration with brain iron accumulation type 4 by mutation in the C19orf12 gene: first time found in adolescent of Russian origin

Maarouf, M

Young adults with dyskinetic cerebral palsy improve subjectively on pallidal stimulation but not in formal dystonia, gait, speech, and swallowing testing

Mache, C

Autologous stem cell transplantation – a therapeutic option in childhood onset chronic inflammatory demyelinating polyneuroradiculopathy?

Mackel, F

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Mader, S

N-Methyl-D-Aspartate Receptor Antibodies in Neuroinflammatory Diseases

Maier, E

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Atypical and mild clinical manifestation in a boy with mitochondrial ATP6 mutation

Maier, O

Atypical Absences, developmental delay, and neonatal diabetes-think of DEND-Syndrome. A Channelopathy involving pancreas, muscle, and brain with possible improvement by sulfonylurea treatment

Neurological symptoms and demyelinating changes on MRI at 3 brothers with cryopyrin-associated periodic syndrome

Evoked potentials in pediatrics: options and limits

MLC-1-related megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap Disease) – a rare cause of macrocephaly and mild motor developmental delay

PNPO mutations in patients with pyridoxine dependent epilepsy

Mainberger, F

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Makowski, C

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Maljevic, S

A mutation in the SCN2A gene associated with BFNIS leads to seizures and behavioral impairment in a mouse model

Mall, V

A physiological characterization of biphasic transcranial magnetic stimulation

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Induction of cortical plasticity by biphasic quadro-pulse stimulation

Interhemispheric connectivity in congenital hemiparesis

Marquard, K

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Biotin-responsive basal ganglia disease in a 10-year-old German girl without SLC19A3 gene mutation

Marquardt, I

Chronic inflammatory demyelinating polyneuropathy (CIDP), Myasthenia gravis and Hashimoto thyroiditis – a very rare coincidence in a 17-year-old patient

Anti-N-methyl-d-aspartate-receptor-encephalitis

Marquardt, T

Quantification of muscular morphological alterations in patients with infantile and early-juvenile Pompe disease

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Martin, F

Congenital myopathy or neurofibromatosis type 1?

Maschke, U

Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism: Phenotypic spectrum of ATP1A3-associated disorders

Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders

Maßmann, K

A double-blinded, randomized, head-to-head trial of levetiracetam versus sulthiame in benign epilepsy with centrotemporal spikes

Maxonus, I

Atypical and mild clinical manifestation in a boy with mitochondrial ATP6 mutation

Maxton, C

Dysphagia following implantation of an vagus nerve stimulator – a case report

May, TW

A double-blinded, randomized, head-to-head trial of levetiracetam versus sulthiame in benign epilepsy with centrotemporal spikes

Mayatepek, E

Transient ischemic attack in a 5-year-old girl due to focal vasculitis in neuroborreliosis

Recurrent fever episodes after treatment of a subdural empyema: persisting infection or autoimmunological reaction?

Biotin-responsive basal ganglia disease: a treatable differential diagnosis of Leigh syndrome

Mayr, J

Autosomal-recessive Kearns-Sayre syndrome is caused by mutations in the RRM2B gene with altered mitochondrial transcription

Atypical and mild clinical manifestation in a boy with mitochondrial ATP6 mutation

Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

Mayr, JA

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Complex I and IV deficiency in an athletic adolescent with mild global retardation, exertional dyspnea, hypertrophic cardiomyopathy, and slight dysdiadochokinesia

Mehraein, Y

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan

Meitinger, T

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype

Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

The German network for mitochondrial disorders (mitoNET)

Melk, A

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Menezes, R

Immediate improvement of paretic hand function after epilepsy surgery in congenital hemiparesis

Mengel, E

Quantification of muscular morphological alterations in patients with infantile and early-juvenile Pompe disease

Mengershausen, U von

Atypical Absences, developmental delay, and neonatal diabetes-think of DEND-Syndrome. A Channelopathy involving pancreas, muscle, and brain with possible improvement by sulfonylurea treatment

Mennecke, A

X-linked Creatine transport deficiency: Phenotypic variability in a family with SLC6A8 gene mutation

Meoded, A

Maturation of the brainstem and cerebellar white matter tracts from the neonatal period to adolescence: a diffusion tensor imaging study

Mergardt, D

Dysphagia following implantation of an vagus nerve stimulator – a case report

Merkenschlager, A

Ambulatory follow-up care of children treated with anticonvulsants and knowledge of parents regarding emergency treatment and safety precautions

Meschede, D

Nicolaides-Baraitser Syndrome

Messmer, C

Central or combined central and peripheral hearing loss at an early born child

Meyer, U

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

Meyer-Osores, A

Lafora disease in a 17-year-old boy due to a compound heterozygous mutation in the NHLRC1 gene

Longitudinal Evaluation of Brain Iron Depositions in a Patient With Confirmed c19orf12 Mutation Using R2* Relaxometry and Quantitative Susceptibility Mapping

Mills, P

PNPO mutations in patients with pyridoxine dependent epilepsy

Moers, A von

Could a mutation in the TGIF-1 gene result in phenotypical expressions like pachygyria, intracerebral calcification, and neonatal epilepsy?

Möhlenbruch, M

Postural headache due to spontaneous intracranial hypotension in an adolescent

Möller-Hartmann, C

Neurodegeneration with brain iron accumulation type 4 by mutation in the C19orf12 gene: first time found in adolescent of Russian origin

Möllers, M

Microcephaly-capillary malformation syndrome: Delineation of a new syndrome

Morava, E

Biotin-responsive basal ganglia disease: a treatable differential diagnosis of Leigh syndrome

Morellini, F

A mutation in the SCN2A gene associated with BFNIS leads to seizures and behavioral impairment in a mouse model

Moret, O

Unusual prodromal manifestation of neuromyelitis optica with prolonged seizures, fever, CSF pleocytosis and encephalopathic EEG-pattern

Morlot, S

Mutation p.Trp3X and mild phenotype of Becker muscular dystrophy

Morris, M

Dopamine-responsive dystonia: Clinical and therapeutic variability with identical genetic defect

Morris-Rosendahl, D

Disequilibrium syndrome caused by an unusual constellation of VLDLR mutations

Microcephaly-capillary malformation syndrome: Delineation of a new syndrome

Effects of CDK5RAP2 downregulation in murine embryonic stem cells correlate with cellular phenotype in MCPH3 patients

Mücke, KH

Herpes simplex virus encephalitis – an unexpected relapse with choreoathetosis

Muehlmann, M

Interhemispheric connectivity in congenital hemiparesis

Mühlfeld, C

Quantification of muscular morphological alterations in patients with infantile and early-juvenile Pompe disease

Mühlhausen, J

Apheresis in the treatment of an acute attack of a demyelinating central nervous system disorder

Müller, A

Refractory epilepsy in a patient with Doose syndrome: favorable response after add-on therapy with bromide

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Different courses of Foix-Chavany-Marie syndrome (FCMS) in children with herpes encephalitis

Müller, C

Case report: cerebral atrophy-induced hygroma in a 3-month-old floppy infant: Unusual and severe manifestation of 5-methylentetrahydrofolate reductase (MTHFR) deficiency

Müller, GA

Apheresis in the treatment of an acute attack of a demyelinating central nervous system disorder

Müller, I

Hematopoietic stem cell transplantation (HSCT) in nine patients with juvenile MLD

Müller, M

Vagal nerve stimulator in childhood absence epilepsy: 2 case reports

Primary central nervous system vasculitis in childhood: more frequent and variable than thought

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Antibodies against Mycoplasma pneumoniae in three patients with meningoencephalitis-causal relationship or epiphenomenon?

Tuberous sclerosis complex-successful therapy with everolimus

Autologous stem cell transplantation – a therapeutic option in childhood onset chronic inflammatory demyelinating polyneuroradiculopathy?

Müller, S

Early white matter changes in childhood multiple sclerosis

Müller-Felber, W

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan

Analysis of myogenic and endothelial progenitor cells in muscle biopsies of juvenile dermatomyositis

Early white matter changes in childhood multiple sclerosis

Case report: oculomotor apraxia in ataxia telangiectasia

Müller-Reible, C

Divergence in clinical presentation of Dynamin2-caused centronuclear myopathy is associated with mutations in distinct parts of the DNM2 gene

Mundt, D

Lacosamide in childhood-results of a retrospective analysis

Nagel, B

Tuberous sclerosis complex-successful therapy with everolimus

Nägele, T

Specific pontine MRI-pattern is a helpful marker to recognize ataxia Charlevoix-Saguenay

Neef, J

Panic attacks in girls with double cortex syndrome: ictal amaurosis

Neininger, MP

Ambulatory follow-up care of children treated with anticonvulsants and knowledge of parents regarding emergency treatment and safety precautions

Neubauer, BA

Mutation analysis of KCNAB1 in rolandic epilepsy

A double-blinded, randomized, head-to-head trial of levetiracetam versus sulthiame in benign epilepsy with centrotemporal spikes

Linear scleroderma en coup de sabre – two case reports with inflammatory CNS lesions

Neubert, G

Effects of CDK5RAP2 downregulation in murine embryonic stem cells correlate with cellular phenotype in MCPH3 patients

Nguyen-Minh, S

A large homozygous microdeletion in the RAB3GAP1 gene causes Warburg Micro syndrome

Ninnemann, O

Effects of CDK5RAP2 downregulation in murine embryonic stem cells correlate with cellular phenotype in MCPH3 patients

Nissen, C

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Noachtar, S

A double-blinded, randomized, head-to-head trial of levetiracetam versus sulthiame in benign epilepsy with centrotemporal spikes

Nolte, K

Central nervous system demyelination complicating Guillain-Barré syndrome

Neurometabolic changes in patients with subacute sclerosing panencephalitis

Normann, C

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Novak, A

Quality of life and mental health of neuropediatric patients

Novotná, B

Rituximab and Cyclophosphamide as an alternative in immunomodulatory therapy in Rasmussen encephalitis

Nürnberg, P

Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism: Phenotypic spectrum of ATP1A3-associated disorders

Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders

Oexle, K

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature

Oh, J

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Ohlenbusch, A

Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders

Ohlmann, JAK

Panic attacks in girls with double cortex syndrome: ictal amaurosis

Olbert, C

Diagnostics and management of pediatric headaches at a University Hospital

Olze, A

Panic attacks in girls with double cortex syndrome: ictal amaurosis

Omran, H

Rare cause of oculomotor palsy

Vitamin B in paediatric neurology

Ketogenic diet in children with pharmacoresistant epilepsy

Opladen, T

Neurometabolic changes in patients with subacute sclerosing panencephalitis

Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene

Tetrahydrobiopterin deficiencies: an international survey of clinical and biochemical features, treatment strategies and follow-up of 626 patients

Otzelberger, B

Quality of life and mental health of neuropediatric patients

Pagel, B

Intra- and cross-modal refractory period effects in healthy children and adults: An ERP study

Paglioli, E

Immediate improvement of paretic hand function after epilepsy surgery in congenital hemiparesis

Palmini, A

Immediate improvement of paretic hand function after epilepsy surgery in congenital hemiparesis

Panzer, A

Could a mutation in the TGIF-1 gene result in phenotypical expressions like pachygyria, intracerebral calcification, and neonatal epilepsy?

Pape, L

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Parkin, N

Congenital myopathy or neurofibromatosis type 1?

Paschke, E

Pyridoxine-dependent epilepsy: case report

PNPO mutations in patients with pyridoxine dependent epilepsy

Pascoal, T

Immediate improvement of paretic hand function after epilepsy surgery in congenital hemiparesis

Paul, K

PNPO mutations in patients with pyridoxine dependent epilepsy

Pauls, A

Young adults with dyskinetic cerebral palsy improve subjectively on pallidal stimulation but not in formal dystonia, gait, speech, and swallowing testing

Paulus, W

Quantification of muscular morphological alterations in patients with infantile and early-juvenile Pompe disease

Pein, H von

Quantification of muscular morphological alterations in patients with infantile and early-juvenile Pompe disease

Pellacani, S

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Peterli, J

Evoked potentials in pediatrics: options and limits

Peters, J

Fatal outcome in a case of recurrent acute necrotizing encephalopathy with RANBP2 gene mutation: importance and difficulty of an early MRI pattern recognition

Philip, S

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Pieper, T

Coincidence of duplication in the PCDH 19 gene and focal cortical dysplasia

Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

Stereo-EEG in children with therapy-refractory epilepsies: Robot-assistance plus stereotaxy combines speed with maximal precision for the implantation of multiple depth electrodes

Piepkorn, M

Herpes simplex virus encephalitis – an unexpected relapse with choreoathetosis

Pietz, J

Implementation of a (neuro-)psychological screening of infants with newly diagnosed epilepsy. Practicability and first results concerning potential premorbid problems

Atypical Infantile neuroaxonal dystrophy: a case report

Behçet disease – a rare differential diagnosis of inflammatory CNS disease in children

Pietzsch, S

Dramatic neurological signs in children with intussusception

Plecko, B

Differential diagnosis of central nervous system vasculopathies: two case reports

PANK2 disease with early onset: clinical and radiologic findings under short term treatment with deferiprone

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings

Infantile choreatic movements, early onset severe epileptic encephalopathy, and primary developmental impairment as a result of a de novo missense mutation in the SCN2A gene

Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich

Pyridoxine-dependent epilepsy: case report

Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

Fatal outcome of rhino-orbital-cerebral mucormycosis due to bilateral internal carotid occlusion in a child after hematopoietic stem cell transplantation

PNPO mutations in patients with pyridoxine dependent epilepsy

Pless, M

Unusual prodromal manifestation of neuromyelitis optica with prolonged seizures, fever, CSF pleocytosis and encephalopathic EEG-pattern

Poggenburg, I

Anti-N-methyl-d-aspartate-receptor-encephalitis

Pohlig, K

Guidelines and examples for orthotic treatment of children and youth in case of myelomeningocele

Polster, T

Microcephaly-capillary malformation syndrome: Delineation of a new syndrome

Pons-Kühnemann, J

Mutation analysis of KCNAB1 in rolandic epilepsy

Poretti, A

Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum

Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

Maturation of the brainstem and cerebellar white matter tracts from the neonatal period to adolescence: a diffusion tensor imaging study

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Porto, L

Atypical case of a neurocutaneous melanosis with typical magnetic resonance imaging findings

Absent biochemical evidence at an early age delayed diagnosis in a patient with a clinically severe form of peroxisomal biogenesis disorder

Poschmann, S

Pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis in a 14-year-old girl probably associated with celiac disease

Prager-Puntigam, S

Vagal nerve stimulator in childhood absence epilepsy: 2 case reports

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Antibodies against Mycoplasma pneumoniae in three patients with meningoencephalitis-causal relationship or epiphenomenon?

Tuberous sclerosis complex-successful therapy with everolimus

Autologous stem cell transplantation – a therapeutic option in childhood onset chronic inflammatory demyelinating polyneuroradiculopathy?

Preisinger, A

Facial nerve palsy in children – is it as benign as supposed?

Preusse, C

Molecular mechanisms of juvenile dermatomyositis

Prietsch, V

Jacobsen syndrome: a rare differential diagnosis of multifocal white matter lesions

Pritsch, M

Acute hemiataxia in childhood

Prokisch, H

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype

Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

The German network for mitochondrial disorders (mitoNET)

Prölß, AK

Quantification of muscular morphological alterations in patients with infantile and early-juvenile Pompe disease

Prott, EC

Nicolaides-Baraitser Syndrome

Prüfer, M

Rituximab and Cyclophosphamide as an alternative in immunomodulatory therapy in Rasmussen encephalitis

Pupp-Peglow, U

Predictors of academic difficulties in preterm children compared with term-born children at the age of 5 years

Püst, B

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Paroxysmal dyskinesia due to PRRT2 mutation in 15-year-old female patient with benign familial infantile convulsions

Isolated trochlear palsy in Lyme disease may persist

13-year-old girl with antiphospholipid antibody-related chorea

Radke, I

Fibroadenoma under therapy with interferons in multiple sclerosis

Rahbek, J

Current care practice in Duchenne muscular dystrophy in Europe – results of the CARE-NMD cross-sectional survey

Ramberger, M

N-Methyl-D-Aspartate Receptor Antibodies in Neuroinflammatory Diseases

Ramisch, EM

Dramatic neurological signs in children with intussusception

Rating, D

Refractory epilepsy in a patient with Doose syndrome: favorable response after add-on therapy with bromide

Rauch, A

Infantile choreatic movements, early onset severe epileptic encephalopathy, and primary developmental impairment as a result of a de novo missense mutation in the SCN2A gene

Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich

Rauchenzauner, M

Activities of daily living in children with hemiparesis: Influence of cognitive functions and motor competence on quality of performance

Rauscher, C

Atypical and mild clinical manifestation in a boy with mitochondrial ATP6 mutation

Razmdjou, S

Bone health and vitamin D metabolism in children and adolescents with Duchenne muscular dystrophy compared with other neuromuscular diseases and cerebral palsy

Reichenbach, JR

Longitudinal Evaluation of Brain Iron Depositions in a Patient With Confirmed c19orf12 Mutation Using R2* Relaxometry and Quantitative Susceptibility Mapping

Reihle, C

Biotin-responsive basal ganglia disease in a 10-year-old German girl without SLC19A3 gene mutation

Reimnitz, D

Hereditary congenital mirror movements

Reindl, M

N-Methyl-D-Aspartate Receptor Antibodies in Neuroinflammatory Diseases

Reinhard, RW

Lyme neuroborreliosis: aetiology and diagnosis of facial palsy in children from Tyrol

Reis, A

Nicolaides-Baraitser Syndrome

Rensing-Zimmermann, C

Bone health and vitamin D metabolism in children and adolescents with Duchenne muscular dystrophy compared with other neuromuscular diseases and cerebral palsy

Rettinger, N

Case report: oculomotor apraxia in ataxia telangiectasia

Reuner, G

Implementation of a (neuro-)psychological screening of infants with newly diagnosed epilepsy. Practicability and first results concerning potential premorbid problems

Reutlinger, C

Dysphagia following implantation of an vagus nerve stimulator – a case report

Riccabona, M

PANK2 disease with early onset: clinical and radiologic findings under short term treatment with deferiprone

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Richter, G

Acute hemiataxia in childhood

Richter, M

Regenerative neuronal proliferation in hypoxic developing mouse brain is transient and modified by erythropoietin treatment

Rieß, A

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan

Ring, E

Tuberous sclerosis complex-successful therapy with everolimus

Röder, B

Intra- and cross-modal refractory period effects in healthy children and adults: An ERP study

Rodger, S

Current care practice in Duchenne muscular dystrophy in Europe – results of the CARE-NMD cross-sectional survey

Rödiger, M

Kleine-Levin syndrome in a 10-year-old boy as the rare cause of hypersomnia

Rödl, T

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan

Rohrbach, M

Myoclonic epilepsy as affection of central nervous system in Farber disease

Ros Cervera, G

Neurological symptoms and demyelinating changes on MRI at 3 brothers with cryopyrin-associated periodic syndrome

Rosewich, H

Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism: Phenotypic spectrum of ATP1A3-associated disorders

Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders

Rossegg, U

Kernicterus: a case study

Transverse myelitis versus encephalitis disseminata

Paroxysmal kinesogenic dyskinesia

Congenital myasthenic syndromes: a difficult approach to diagnosis and therapy

13-year-old patient with headache, unclear on/off symptoms and psychosocial burden

Ischemic Stroke in a 14-year-old Boy with Homozygous C677T MTHFR Mutation

Rost, I

Heterozygous deletion of exon 3 of phospholipase C β1 gene causes neonatal epileptic encephalopathy?

Rostásy, K

Status epilepticus caused by hypocalcaemia in a 6-month old child with hypoparathyroidism

Analysis of myogenic and endothelial progenitor cells in muscle biopsies of juvenile dermatomyositis

Neuropsychological long-term outcome in children with SVT

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings

Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum

Epileptic seizures and chromosomal microdeletions/duplications

Visual disorders in children with cerebral palsy

Epilepsy in children with cerebral palsy

Central nervous system demyelination complicating Guillain-Barré syndrome

Jeavon syndrome as a differential diagnosis of facial tics

Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease

Predictors of academic difficulties in preterm children compared with term-born children at the age of 5 years

N-Methyl-D-Aspartate Receptor Antibodies in Neuroinflammatory Diseases

Editorial

Rötig, A

Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

Rückriegel, S

Frontocerebellar tract lesions revealed by tractography in pediatric posterior fossa tumor survivors

Rudnik-Schöneborn, S

Specific pontine MRI-pattern is a helpful marker to recognize ataxia Charlevoix-Saguenay

Ruf, S

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Saadi, S

Pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis in a 14-year-old girl probably associated with celiac disease

Saake, M

X-linked Creatine transport deficiency: Phenotypic variability in a family with SLC6A8 gene mutation

Sánchez Albisua, I

Natural course of pontocerebellar hypoplasia Type 2

Specific pontine MRI-pattern is a helpful marker to recognize ataxia Charlevoix-Saguenay

Sánchez Fernández, I

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Sanford, L

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Santer, R

Hematopoietic stem cell transplantation (HSCT) in nine patients with juvenile MLD

Santorelli, FM

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Sarikaya, S

Recurrent fever episodes after treatment of a subdural empyema: persisting infection or autoimmunological reaction?

Sarnat, HB

Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

Sassen, R

Lacosamide in childhood-results of a retrospective analysis

Saurenmann, T

Differential diagnosis of central nervous system vasculopathies: two case reports

Saxena, A

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Schaffer, M

Treatment of therapy-resistant sialorrhea with transdermal scopolamine in a 10-year-old girl with Wolf-Hirschhorn syndrome

Schallner, J

Hypertrophic olivary degeneration: a differential diagnosis to consider following surgical intervention in the posterior cranial fossa: review and two case reports

Schallner, JC

Central nervous system autoimmune syndrome associated with neuronal surface antibodies in the course of Enterovirus encephalitis

Schanda, K

N-Methyl-D-Aspartate Receptor Antibodies in Neuroinflammatory Diseases

Schänzer, A

Quantification of muscular morphological alterations in patients with infantile and early-juvenile Pompe disease

Schaper, J

Transient ischemic attack in a 5-year-old girl due to focal vasculitis in neuroborreliosis

Recurrent fever episodes after treatment of a subdural empyema: persisting infection or autoimmunological reaction?

Biotin-responsive basal ganglia disease: a treatable differential diagnosis of Leigh syndrome

Schara, U

Molecular mechanisms of juvenile dermatomyositis

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan

Alpha-dystroglycanopathies: Clinical and genetic variability

Tetrasomy X and neuropathy: double trouble or extended phenotype?

Neurodegeneration with brain iron accumulation type 4 by mutation in the C19orf12 gene: first time found in adolescent of Russian origin

Scheer, I

Differential diagnosis of central nervous system vasculopathies: two case reports

Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich

Fatal outcome of rhino-orbital-cerebral mucormycosis due to bilateral internal carotid occlusion in a child after hematopoietic stem cell transplantation

Scheffner, T

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Schell-Apacik, C

Could a mutation in the TGIF-1 gene result in phenotypical expressions like pachygyria, intracerebral calcification, and neonatal epilepsy?

Schettler, KF

Dramatic neurological signs in children with intussusception

Schimmel, M

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings

Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease

Uncommon presentation of voltage-gated potassium channel complex-antibody mediated central nervous system disease with eye movement disorder and ataxia

Schlachter, K

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Schlotawa, L

Disequilibrium syndrome caused by an unusual constellation of VLDLR mutations

Schmidt, I

Muscle-specific discordant skewing of X-chromosome inactivation leads to different clinical phenotypes of Duchenne muscular dystrophy in two monozygotic female twins

Schmidt, WM

Muscle-specific discordant skewing of X-chromosome inactivation leads to different clinical phenotypes of Duchenne muscular dystrophy in two monozygotic female twins

Schmiedel, G

PNPO mutations in patients with pyridoxine dependent epilepsy

Schmitt, B

Infantile choreatic movements, early onset severe epileptic encephalopathy, and primary developmental impairment as a result of a de novo missense mutation in the SCN2A gene

Impairment of synaptic downscaling: A potential mechanism for neuropsychological deficits in continuous spike waves during slow wave sleep

Schmitt, K

Transverse myelitis versus encephalitis disseminata

Paroxysmal kinesogenic dyskinesia

Congenital myasthenic syndromes: a difficult approach to diagnosis and therapy

Facial nerve palsy in children – is it as benign as supposed?

Ischemic Stroke in a 14-year-old Boy with Homozygous C677T MTHFR Mutation

Schmitt-Mechelke, T

Primary central nervous system vasculitis in childhood: more frequent and variable than thought

Schmitz, N

Myoclonic epilepsy as affection of central nervous system in Farber disease

Schnakenbeurg, C von

Diagnostics and management of pediatric headaches at a University Hospital

Schneider, HC

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Schneider, JF

Complex I and IV deficiency in an athletic adolescent with mild global retardation, exertional dyspnea, hypertrophic cardiomyopathy, and slight dysdiadochokinesia

Schnekenbühl, S

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Schober, H

Benign partial epilepsy of infancy as defined by Watanabe: 2 case reports

Pyridoxine-dependent epilepsy: case report

Weakness of the limb girdle type with finger tremor and elevated creatine kinase

Schoberer, M

Central nervous system demyelination complicating Guillain-Barré syndrome

Scholl Bürgi, S

Epileptic seizures and chromosomal microdeletions/duplications

Schönau, E

Young adults with dyskinetic cerebral palsy improve subjectively on pallidal stimulation but not in formal dystonia, gait, speech, and swallowing testing

Schönberger, J

Postural headache due to spontaneous intracranial hypotension in an adolescent

Schöner, A

Connatal brain hemorrhage as fetal manifestation of Osler-Weber-Rendu syndrome (hereditary hemorrhagic telangiectasia)

Schöning, M

Specific pontine MRI-pattern is a helpful marker to recognize ataxia Charlevoix-Saguenay

Schoser, B

Molecular mechanisms of juvenile dermatomyositis

Analysis of myogenic and endothelial progenitor cells in muscle biopsies of juvenile dermatomyositis

Schotten, KJ

A double-blinded, randomized, head-to-head trial of levetiracetam versus sulthiame in benign epilepsy with centrotemporal spikes

Schöttler-Glas, A

Characteristic MRI finding in severe tick-borne encephalitis in children and the effect of immunoglobulin G on the course of the disease

Schröder, C

Sturge-Weber syndrome with hyposomatotropism

Schröder, S

Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders

Schroeder, AS

Early white matter changes in childhood multiple sclerosis

Schroeder, S

Which covariates influence effectiveness of intensified robotic-assisted treadmill therapy in children with cerebral palsy

Schrum, J

Hematopoietic stem cell transplantation (HSCT) in nine patients with juvenile MLD

Schubert, M

Quality of life and mental health of neuropediatric patients

Schubert-Bast, S

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings

Lacosamide in childhood-results of a retrospective analysis

Implementation of a (neuro-)psychological screening of infants with newly diagnosed epilepsy. Practicability and first results concerning potential premorbid problems

Case report: cerebral atrophy-induced hygroma in a 3-month-old floppy infant: Unusual and severe manifestation of 5-methylentetrahydrofolate reductase (MTHFR) deficiency

Schuler, E

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings

Atypical Infantile neuroaxonal dystrophy: a case report

Behçet disease – a rare differential diagnosis of inflammatory CNS disease in children

Schülke, M

Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease

Schulz, A

DEM-CHILD – a treatment-oriented research project of NCL disorders as a major cause of dementia in childhood

Longitudinal Evaluation of Brain Iron Depositions in a Patient With Confirmed c19orf12 Mutation Using R2* Relaxometry and Quantitative Susceptibility Mapping

Schuster, M

Central or combined central and peripheral hearing loss at an early born child

Schütz, C

Implementation of a (neuro-)psychological screening of infants with newly diagnosed epilepsy. Practicability and first results concerning potential premorbid problems

Schwartz, O

Ketogenic diet in children with pharmacoresistant epilepsy

Schwarz, R

Kernicterus: a case study

Transverse myelitis versus encephalitis disseminata

Steroids can influence the outcome of acute necroting encephalopathy

Congenital myasthenic syndromes: a difficult approach to diagnosis and therapy

Schwarz, T

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Schwarzmayr, T

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Schwerin-Nagel, A

Vagal nerve stimulator in childhood absence epilepsy: 2 case reports

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Tuberous sclerosis complex-successful therapy with everolimus

Autologous stem cell transplantation – a therapeutic option in childhood onset chronic inflammatory demyelinating polyneuroradiculopathy?

Schweser, F

Longitudinal Evaluation of Brain Iron Depositions in a Patient With Confirmed c19orf12 Mutation Using R2* Relaxometry and Quantitative Susceptibility Mapping

Schwindt, W

Rare cause of oculomotor palsy

Ocular myositis

Schwinger, W

Autologous stem cell transplantation – a therapeutic option in childhood onset chronic inflammatory demyelinating polyneuroradiculopathy?

Sedlacik, J

Longitudinal Evaluation of Brain Iron Depositions in a Patient With Confirmed c19orf12 Mutation Using R2* Relaxometry and Quantitative Susceptibility Mapping

Seidel, C

Ocular myasthenia with both AChR and MuSK antibodies

Seidel, MG

Autologous stem cell transplantation – a therapeutic option in childhood onset chronic inflammatory demyelinating polyneuroradiculopathy?

Seidel, U

Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease

Seidl, R

Muscle-specific discordant skewing of X-chromosome inactivation leads to different clinical phenotypes of Duchenne muscular dystrophy in two monozygotic female twins

Quality of life and mental health of neuropediatric patients

Seiler, A

Effects of CDK5RAP2 downregulation in murine embryonic stem cells correlate with cellular phenotype in MCPH3 patients

Seitz, A

Postural headache due to spontaneous intracranial hypotension in an adolescent

Seufert, J

Bone health and vitamin D metabolism in children and adolescents with Duchenne muscular dystrophy compared with other neuromuscular diseases and cerebral palsy

Severien, C

Biotin-responsive basal ganglia disease in a 10-year-old German girl without SLC19A3 gene mutation

Sibon, O

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation

Siebner, H

A physiological characterization of biphasic transcranial magnetic stimulation

Siegel, C

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature

Sigl-Baumgartner, S

Neuropsychological long-term outcome in children with SVT

Sigler, M

Apheresis in the treatment of an acute attack of a demyelinating central nervous system disorder

Simma, B

Benign partial epilepsy of infancy as defined by Watanabe: 2 case reports

Pyridoxine-dependent epilepsy: case report

Weakness of the limb girdle type with finger tremor and elevated creatine kinase

Smitka, M

Hypertrophic olivary degeneration: a differential diagnosis to consider following surgical intervention in the posterior cranial fossa: review and two case reports

Mycoplasma pneumoniae and Borrelia burgdorferi as cause for facial paralysis in children: single-center experience of 10 years

Central nervous system autoimmune syndrome associated with neuronal surface antibodies in the course of Enterovirus encephalitis

Rituximab and Cyclophosphamide as an alternative in immunomodulatory therapy in Rasmussen encephalitis

Soelva, V

Frontocerebellar tract lesions revealed by tractography in pediatric posterior fossa tumor survivors

Sorantin, E

Autologous stem cell transplantation – a therapeutic option in childhood onset chronic inflammatory demyelinating polyneuroradiculopathy?

Specht, S

Anti-N-methyl-d-aspartate-receptor encephalitis in a patient with acute organic brain syndrome with catatonia

Sperl, W

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Atypical and mild clinical manifestation in a boy with mitochondrial ATP6 mutation

Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype

Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

The German network for mitochondrial disorders (mitoNET)

Spiegler, J

Do developmental problems perceived by parents of very-low-birth weight infants during the first year of life correlate with objective criteria at 2 years of age?

Contactin-associated protein-like 2 antibodies (CASPR2) encephalopathy in 3-year-old dizygotic twins

Spors, B

A large homozygous microdeletion in the RAB3GAP1 gene causes Warburg Micro syndrome

Spranger, S

Heterozygous deletion of exon 3 of phospholipase C β1 gene causes neonatal epileptic encephalopathy?

Spreiz, A

Epileptic seizures and chromosomal microdeletions/duplications

Familial occurrence of a 16p13 microdeletion including GRIN2A as a cause of developmental delay and epilepsy with continuous spike and waves during sleep

Srivastava, R

Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease

Stange, M

Sturge-Weber syndrome with hyposomatotropism

Staudt, M

Refractory epilepsy in a patient with Doose syndrome: favorable response after add-on therapy with bromide

Coincidence of duplication in the PCDH 19 gene and focal cortical dysplasia

Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

Intraventricular baclofen therapy in refractory secondary dystonia-Indication, methodology, safety, and first results

Stereo-EEG in children with therapy-refractory epilepsies: Robot-assistance plus stereotaxy combines speed with maximal precision for the implantation of multiple depth electrodes

Activities of daily living in children with hemiparesis: Influence of cognitive functions and motor competence on quality of performance

Severe dystonia caused by hemolytic-uremic syndrome with characteristic MRI scans

Immediate improvement of paretic hand function after epilepsy surgery in congenital hemiparesis

Interhemispheric connectivity in congenital hemiparesis

Outcome measurement in clinical pediatric neurorehabilitation: assessment of motor and process skills evaluates the effect of therapy in the area of activity of daily living

Characteristic MRI finding in severe tick-borne encephalitis in children and the effect of immunoglobulin G on the course of the disease

Different courses of Foix-Chavany-Marie syndrome (FCMS) in children with herpes encephalitis

Confirmation of congenital mirror movements in a 19-month-old boy by detection of a de novo DCC mutation

Steffensen, B

Current care practice in Duchenne muscular dystrophy in Europe – results of the CARE-NMD cross-sectional survey

Steinbeis-von Stülpnagel, C

Lafora disease in a 17-year-old boy due to a compound heterozygous mutation in the NHLRC1 gene

Steiner, C

Absent biochemical evidence at an early age delayed diagnosis in a patient with a clinically severe form of peroxisomal biogenesis disorder

Steinfeld, R

Stepwise adaptation of treatment with calcium folinate in different modes of application leads to optimal therapeutic results for patients with cerebral folate transport deficiency

Stenzel, W

Molecular mechanisms of juvenile dermatomyositis

Stephani, U

German-wide survey on the management of status epilepticus in children

Steuernagel, P

Connatal brain hemorrhage as fetal manifestation of Osler-Weber-Rendu syndrome (hereditary hemorrhagic telangiectasia)

Stockler, S

PNPO mutations in patients with pyridoxine dependent epilepsy

Stöckler, S

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

Stodieck, S

Paroxysmal dyskinesia due to PRRT2 mutation in 15-year-old female patient with benign familial infantile convulsions

Stoffels, J

Pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis in a 14-year-old girl probably associated with celiac disease

Striano, P

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Strobl, K

Panic attacks in girls with double cortex syndrome: ictal amaurosis

Strobl, W

Results of calcaneo stop arthroereisis in children with neuromotoric disorders

Strobl, WM

Guidelines and examples for orthotic treatment of children and youth in case of myelomeningocele

Stroet, A

A prospective study on 71 children to investigate normative pediatric values in optical coherence tomography

Strom, T

Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

Strom, TM

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Struys, E

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

PNPO mutations in patients with pyridoxine dependent epilepsy

Stülpnagel, C von

Refractory epilepsy in a patient with Doose syndrome: favorable response after add-on therapy with bromide

Characteristic MRI finding in severe tick-borne encephalitis in children and the effect of immunoglobulin G on the course of the disease

Stummer, W

Rare cause of oculomotor palsy

Stüve, B

Nicolaides-Baraitser Syndrome

Synofzik, M

Specific pontine MRI-pattern is a helpful marker to recognize ataxia Charlevoix-Saguenay

Syrbe, S

Ambulatory follow-up care of children treated with anticonvulsants and knowledge of parents regarding emergency treatment and safety precautions

Tacke, U

Diagnostics and management of pediatric headaches at a University Hospital

Talmon l'Armée, E

Different courses of Foix-Chavany-Marie syndrome (FCMS) in children with herpes encephalitis

Tappauf, M

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Antibodies against Mycoplasma pneumoniae in three patients with meningoencephalitis-causal relationship or epiphenomenon?

Tardieu, M

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings

Tauer, U

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature

Theophil, M

Could a mutation in the TGIF-1 gene result in phenotypical expressions like pachygyria, intracerebral calcification, and neonatal epilepsy?

Thiede, A

Successful therapy with individualized combined speech-and-stutter therapy, psychological motivation, and learning help for an 11-years-old girl with cerebral palsy

Thiele, H

Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism: Phenotypic spectrum of ATP1A3-associated disorders

Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders

Thiels, C

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt

Methylenetetrahydrofolate reductase deficiency: therapy and outcome (with video)

Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene

Visual impairment – differential diagnoses

Thomale, U

Frontocerebellar tract lesions revealed by tractography in pediatric posterior fossa tumor survivors

Timmermann, L

Young adults with dyskinetic cerebral palsy improve subjectively on pallidal stimulation but not in formal dystonia, gait, speech, and swallowing testing

Tiranti, V

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Toelle, SP

Fatal outcome of rhino-orbital-cerebral mucormycosis due to bilateral internal carotid occlusion in a child after hematopoietic stem cell transplantation

Treumann, T

Primary central nervous system vasculitis in childhood: more frequent and variable than thought

Trippe, H

Alpha-dystroglycanopathies: Clinical and genetic variability

Tetrasomy X and neuropathy: double trouble or extended phenotype?

Trollmann, R

Regenerative neuronal proliferation in hypoxic developing mouse brain is transient and modified by erythropoietin treatment

Interplay of inflammation and hypoxia in perinatal brain injury

Closure of meningomyeloceles with the 4-flap compound technique according to Ramirez

Ultrasound-guided neuronavigation-the safest approach for Rickham capsule insertion in preterm infants

X-linked Creatine transport deficiency: Phenotypic variability in a family with SLC6A8 gene mutation

Tschiderer, B

Visual disorders in children with cerebral palsy

Tuxhorn, I

A double-blinded, randomized, head-to-head trial of levetiracetam versus sulthiame in benign epilepsy with centrotemporal spikes

Twilt, M

Pediatric neuromyelitis optica-beyond the optic nerve and spinal cord

Urban, C

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Utermann, G

Epileptic seizures and chromosomal microdeletions/duplications

Utzig, N

Sturge-Weber syndrome with hyposomatotropism

Valente, EM

Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

van Baalen, A

German-wide survey on the management of status epilepticus in children

Lacosamide in childhood-results of a retrospective analysis

Van Hove, J

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

van Karnebeek, C

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

van Moers, A

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Vermeulen, J

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Vieker, S

Lacosamide in childhood-results of a retrospective analysis

Viemann, M

Connatal brain hemorrhage as fetal manifestation of Osler-Weber-Rendu syndrome (hereditary hemorrhagic telangiectasia)

Vietzke, D

Recurrent fever episodes after treatment of a subdural empyema: persisting infection or autoimmunological reaction?

Vorgerd, M

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt

Vry, J

Current care practice in Duchenne muscular dystrophy in Europe – results of the CARE-NMD cross-sectional survey

Wagentristl, HP

Atypical and mild clinical manifestation in a boy with mitochondrial ATP6 mutation

Wagner, M

Intraventricular baclofen therapy in refractory secondary dystonia-Indication, methodology, safety, and first results

Wallis, J

Contactin-associated protein-like 2 antibodies (CASPR2) encephalopathy in 3-year-old dizygotic twins

Walsh, S

Hypertrophic olivary degeneration: a differential diagnosis to consider following surgical intervention in the posterior cranial fossa: review and two case reports

Walther, A

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Waltz, S

Nicolaides-Baraitser Syndrome

Wanschitz, J

Analysis of myogenic and endothelial progenitor cells in muscle biopsies of juvenile dermatomyositis

Warken, B

Which covariates influence effectiveness of intensified robotic-assisted treadmill therapy in children with cerebral palsy

Warmuth-Metz, M

Hypertrophic olivary degeneration: a differential diagnosis to consider following surgical intervention in the posterior cranial fossa: review and two case reports

Weber, K

Different courses of Foix-Chavany-Marie syndrome (FCMS) in children with herpes encephalitis

Weber, Y

Ocular myositis

Wegendt, C

Microcephaly-capillary malformation syndrome: Delineation of a new syndrome

Wehrmann, C

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Wei, XC

Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum

Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

Weigt-Usinger, K

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt

Methylenetetrahydrofolate reductase deficiency: therapy and outcome (with video)

A prospective study on 71 children to investigate normative pediatric values in optical coherence tomography

Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene

Stepwise adaptation of treatment with calcium folinate in different modes of application leads to optimal therapeutic results for patients with cerebral folate transport deficiency

Visual impairment – differential diagnoses

Weis, J

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Weissensteiner, M

Kernicterus: a case study

Werneck, H

Quality of life and mental health of neuropediatric patients

Wickede, M von

Fatal outcome in a case of recurrent acute necrotizing encephalopathy with RANBP2 gene mutation: importance and difficulty of an early MRI pattern recognition

Wiegand, G

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Wieland, T

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature

Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Wiemer-Kruel, A

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Panic attacks in girls with double cortex syndrome: ictal amaurosis

Wiesinger-Eidenberger, G

Kernicterus: a case study

Wilichowski, E

Autosomal-recessive Kearns-Sayre syndrome is caused by mutations in the RRM2B gene with altered mitochondrial transcription

Divergence in clinical presentation of Dynamin2-caused centronuclear myopathy is associated with mutations in distinct parts of the DNM2 gene

Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype

Wilke, M

Increasing prematurity is associated with a more pronounced delay in brain maturation in older children and adolescents

Interhemispheric connectivity in congenital hemiparesis

Will, B

Lambdoid synostosis or positional plagiocephaly – a visual diagnosis?

Wille, DA

Infantile choreatic movements, early onset severe epileptic encephalopathy, and primary developmental impairment as a result of a de novo missense mutation in the SCN2A gene

Winkler, A

Increasing prematurity is associated with a more pronounced delay in brain maturation in older children and adolescents

Witsch-Baumgartner, M

Weakness of the limb girdle type with finger tremor and elevated creatine kinase

Witt, O

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Wittig, I

The German network for mitochondrial disorders (mitoNET)

Wohlrab, G

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings

Myoclonic epilepsy as affection of central nervous system in Farber disease

Wolf, N

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

PNPO mutations in patients with pyridoxine dependent epilepsy

Wolf, P

Stepwise adaptation of treatment with calcium folinate in different modes of application leads to optimal therapeutic results for patients with cerebral folate transport deficiency

Acute hemiataxia in childhood

Wolff, M

Early childhood onset progressive myoclonic epilepsy phenotype caused by KCTD7 mutations

Lambdoid synostosis or positional plagiocephaly – a visual diagnosis?

Würfel, E

Evidence against the concept of chronic cerebrospinal venous insufficiency in multiple sclerosis

Würfel, J

Evidence against the concept of chronic cerebrospinal venous insufficiency in multiple sclerosis

Xompero, F

A mutation in the SCN2A gene associated with BFNIS leads to seizures and behavioral impairment in a mouse model

Yeh, EA

Plasma exchange in pediatric central nervous system inflammatory demyelination

Pediatric neuromyelitis optica-beyond the optic nerve and spinal cord

Zabel, B

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Zanni, G

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Zaugg, C

Dopamine-responsive dystonia: Clinical and therapeutic variability with identical genetic defect

Zebedin, D

Tuberous sclerosis complex-successful therapy with everolimus

Zeches-Kánsy, C

Characteristic MRI finding in severe tick-borne encephalitis in children and the effect of immunoglobulin G on the course of the disease

Zeiner, F

Cardiomyopathy in a patient with Mb Duchenne first presenting as myocardial infarction in childhood

Zellner, A

Lacosamide in childhood-results of a retrospective analysis

Zenz, W

Antibodies against Mycoplasma pneumoniae in three patients with meningoencephalitis-causal relationship or epiphenomenon?

Zernikow, B

Quantitative sensory testing in children and adolescents with tension type headache: changes in nociceptive processing are not specific for migraine

Zerres, K

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Zeschnigk, C

Disequilibrium syndrome caused by an unusual constellation of VLDLR mutations

Zimmerhackl, LB

Lyme neuroborreliosis: aetiology and diagnosis of facial palsy in children from Tyrol

Zimmermann, F

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Zirn, S

Central or combined central and peripheral hearing loss at an early born child

Zotter, S

Neuropsychological long-term outcome in children with SVT

Epileptic seizures and chromosomal microdeletions/duplications

Predictors of academic difficulties in preterm children compared with term-born children at the age of 5 years

Zschocke, J

Epileptic seizures and chromosomal microdeletions/duplications

Familial occurrence of a 16p13 microdeletion including GRIN2A as a cause of developmental delay and epilepsy with continuous spike and waves during sleep

Zweier, C

Nicolaides-Baraitser Syndrome