Abstracts of the 38th Annual Meeting of the Society of Neuropediatrics

Adler, C

Hand function after disconnection of the primary somatosensory representation as a consequence of hemispherotomy

Ipsilateral Motor Control Without Mirror Movements?

Aksu, F

Peroneal nerve palsy pointing towards a cerebral disorder

Impaired Control of Respiration as Crucial Evidence for Pitt-Hopkins Syndrome

Albers, J

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Albrecht, B

Deletion 22q13 (Phelan-McDermid-Syndrom) in two children with delayed development of speech and muscular hypotonia

Allkemper, T

Is neuritis nervi optici in children a predictor of multiple sclerosis in adulthood?

Alperin, N

Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis

Total cerebral blood flow during childhood and adolescence as assessed with phase-contrast imaging

Althaus, J

Ataxia Telangiectasia (AT) as a radiation sensitivity syndrom and limits of radiotherapeutic intervention

Alzheimer, C

Age dependent regulation of the neuroprotective factor activin in the mouse brain

Andresen, F

Minimal invasive fetoscopic closure of myelomeningocele – postoperative care and interdisciplinary disease-management

Arnig, L

Elevated alpha fetoprotein as indicator for ataxia with oculomotor apraxia type 2 (AOA2)

Arning, L

Ring chromosome 22 and neurofibromatosis type II: proof of two hit model for the loss of the NF2 gene in the development of meningioma

Arnold, R

Mowat-Wilson Syndrome, a rare genetic condition with intestinal and cerebral symptoms

Assmann, B

Brown-Vialetto-Van Laere syndrome: A riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene

Au, K von

Growth and psychomotor development of patients with Duchenne Muscular Dystrophy

Aznar Lain, G

Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity

Bächli, H

Minimal invasive fetoscopic closure of myelomeningocele – postoperative care and interdisciplinary disease-management

Baethmann, M

Gastroenteritis associated encephalopathy with reversible splenial lesion: three cases

Banwell, B

Hiccups, Vomiting and the Brain

Barkmann, C

Statistical properties of the jNCL scoring system according to Kohlschütter (1988)

Bartels, I

Ring chromosome 22 and neurofibromatosis type II: proof of two hit model for the loss of the NF2 gene in the development of meningioma

Array CGH in children and adolescents with developmental delay or intellectual disability: are there phenotypic clues to clinically relevant chromosomal microaberrations?

Barthelmie, A

Focal epilepsy caused by multiple cavernous hemangiomas and mental retardation – successful therapy and genetic cause (CCM3)

Deletion 22q13 (Phelan-McDermid-Syndrom) in two children with delayed development of speech and muscular hypotonia

Bast, T

Clinical characterization of myoclonic-astatic epilepsy

Baumann, M

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Bäumel, C

3D-Television and the Risk of Seizures in Children

Baumgart, A

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Baumgartner, M

Male Rett Syndrome – genetic diagnosis using oral mucosa swabs

Baumgartner, S

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Baz-Bartels, M

Ataxia Telangiectasia (AT) as a radiation sensitivity syndrom and limits of radiotherapeutic intervention

Becher, T

Neuroborreliosis without Neurology?!

Focal epilepsy caused by multiple cavernous hemangiomas and mental retardation – successful therapy and genetic cause (CCM3)

Beck, M

Respiration and its correlation with motoric function in non-classic Pompe disease

Treatment of Lysosomal Storage Disorders: Presence and Future

Berghoff, M

mRNA-expression patterns of Fas and its signalling cascade in Multiple Sclerosis (MS) and Experimental Autoimmune Encephalomyelitis (EAE)

Bernhard, M

Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?

Shaking the head without end – bobble-head doll syndrome in no-no direction

Bertsche, A

Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?

Shaking the head without end – bobble-head doll syndrome in no-no direction

Berweck, S

Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis

Long-term Outcome after Vegetative State due to Near-Drowning and Quality of Life of the Families

Ipsilateral Motor Control Without Mirror Movements?

Bettendorf, U

Influence of antiepileptic treatment on bone metabolism

Bevot, A

Relationship between growth and psychomotor development of preterm children

Beytia, M

Manifestation of muscular dystrophy by Anoctamin-5 mutation in infancy

Biebl, A

Prospective analysis on brain MRI in children with neurological disease

Bierbaum, A

Laterality, bimanual interference and short-term motor learning of fine motor movements in childhood and adolescence

Biesecker, L

A postzygotic activating AKT1 mutation in a discordant monozygotic twin with Proteus syndrome

Bigi, S

Hiccups, Vomiting and the Brain

Binggeli, R

Neuroleptic Malignant Syndrome due to Tetrabenazine in a Boy with a Subacute Extrapyramidal Disorder

Biskup, S

A familial epilepsy with behavioural features associated with a PCDH19 mutation

Bittner, R

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Blankenburg, M

Peroneal nerve palsy pointing towards a cerebral disorder

Impaired Control of Respiration as Crucial Evidence for Pitt-Hopkins Syndrome

Blaschek, A

Familial mutation in ACTA1 gene – clinical variability

Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis

Multiple sclerosis and periodic fever syndromes: Characterization of clinical symptoms

Blassnig-Ezeh, A

Central nervous system Lyme disease – Presentation of two cases

Bode, H

Predictors of comorbid psychiatric disorders in children and adolescents with cerebral palsy. Impact on family burden and quality of life. Results of a multicenter study

Böhm, R

Symptomatic Treatment of Tomaculous Polyneuropathy with Methylprednisolone

Böhringer, E

Isolated neonatal bilateral palsy of the n. radialis; case report and review of the literature

Mosaic ring chromosome 3 in a child with epilepsy and developmental delay

Boltshauser, E

Isolated spinal juvenile xanthogranuloma in an infant presenting as acute paraplegia

Oral-Facial-Digital Syndrome Type VI: Delineation and Diagnostic Criteria

Macrocerebellum: not a clinical and neuroimaging entity

Behavioural changes and unilateral movement disorder in 2 adolescents with Chorea Sydenham

Bannayan-Riley-Ruvalcaba-Syndrom with progressive spinal epidural lipomatosis

Bonin, M

Large interstitial duplication in the LARGE-gene in a patient with Walker-Warburg-syndrome.

Bönnemann, C

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Boor, R

Clinical characterization of myoclonic-astatic epilepsy

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Borggräfe, I

Immunoadsorption in refractory status epilepticus related to NMDAR-Encephalitis

Presurgical evaluation in refractory epilepsy in toddlers with depths electrodes

Borusiak, P

Influence of antiepileptic treatment on bone metabolism

Bozinov, O

Isolated spinal juvenile xanthogranuloma in an infant presenting as acute paraplegia

Brackmann, F

Age dependent regulation of the neuroprotective factor activin in the mouse brain

Brentrup, A

Rare course of an intraspinal dermoid

Brockmann, K

Array CGH in children and adolescents with developmental delay or intellectual disability: are there phenotypic clues to clinically relevant chromosomal microaberrations?

A familial epilepsy with behavioural features associated with a PCDH19 mutation

A postzygotic activating AKT1 mutation in a discordant monozygotic twin with Proteus syndrome

Broser, P

Lateralization of language pathways in children as assessed using fMRI-guided probabilistic tractography

Brueckner, F

Pseudotumor cerebri in an 8 month old infant

Brüggemann, N

Do young adolescents with periodic ataxia due to GLUT-1 Deficiency profit from introduction of a modified Atkins Diet?

Brunner-Krainz, M

CT Perfusion and CT Angiography in children and juvenile patients during an attack of migraine with aura

Chronic inflammatory bowel disease and cerebrovascular insults in a pediatric patient: a case report

Bannayan-Riley-Ruvalcaba-Syndrome – a rare differential diagnosis in children with macrocephaly

Budde, J

Pseudotumor cerebri under prednisolone treatment for infantile spasms

Bültmann, E

Fluctuating N IV paresis as presenting sign of a brain stem tumor: two pediatric cases

Burfeind, P

Array CGH in children and adolescents with developmental delay or intellectual disability: are there phenotypic clues to clinically relevant chromosomal microaberrations?

Burger, H

Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis

Burghardt, R

Laterality, bimanual interference and short-term motor learning of fine motor movements in childhood and adolescence

Bürki, S

Video documentation of a case of Dopa responsive Dystonia in early infancy: a rare but important diagnosis

Bußmann, C

Leukoencephalopathy with metaphyseal chondrodysplasia

Buyse, G

DELOS Phase III Study with Idebenone (Catena®) in Duchenne Muscular Dystrophy

Carlens, J

Fluctuating N IV paresis as presenting sign of a brain stem tumor: two pediatric cases

Cirak, S

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Clas, P

Metachromatic Leukodystrophy – cerebral grey and white matter volume changes and clinical course

Classen, G

Symptomatic Treatment of Tomaculous Polyneuropathy with Methylprednisolone

Colombi, M

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Czermin, B

FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment

Das, A

Fluctuating N IV paresis as presenting sign of a brain stem tumor: two pediatric cases

Datta, A

Mosaic ring chromosome 3 in a child with epilepsy and developmental delay

Dehn, L

Burdens of parents with epileptic children – Results of a study using a short-form of the German version of the Impact-on-Family-Scale

Della Marina, A

Myasthenia gravis in an 22 months-old girl – impressing improvement due to early adaequate therapy

A 16 year-old patient presenting with Lambert-Eaton myasthenic syndrome

Myasthenia gravis in young children and adolescents: clinical signs and treatment options

Delvendahl, I

Attention deficit in patients with Noonan Syndrome (NS)

der Hagen, M von

Measuring quality of life in patients with life-limiting neuromuscular disorders: a pilot study using the Kidscreen-27- and KINDL-R-questionnaire

Hypocretin-level during therapy with intravenous immunglobulines in an early stage of narcolepsy with cataplexy in childhood

The pathogenesis and phenotype of children with microcephaly – Retrospective analysis and development of a microcephaly database

The pathogenesis and phenotype of children with microcephaly (MC) – Establishment of a multi-center microcephaly database (Department of Child Neurology in Berlin 2000–2010)

Growth and psychomotor development of patients with Duchenne Muscular Dystrophy

Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia

Acetazolamide as treatment for GLUT1 deficiency syndrome?

Dertinger, S

Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities

Deutschmann, A

Chronic inflammatory bowel disease and cerebrovascular insults in a pediatric patient: a case report

Deutz, U

Bannayan-Riley-Ruvalcaba-syndrom – an unusual differential diagnosis of dilatated Virchow-Robin spaces

Di Donato, N

The pathogenesis and phenotype of children with microcephaly – Retrospective analysis and development of a microcephaly database

Dietz, B

Peroneal nerve palsy pointing towards a cerebral disorder

Impaired Control of Respiration as Crucial Evidence for Pitt-Hopkins Syndrome

Distelmaier, F

Sudden bilateral sensorineural deafness in a 5 years old girl with blue sclerae, keratoconus, hypermobility of the joints and hyperelasticity of the skin with a mutation in the ZNF469 gene encoding for Brittle-Cornea-Syndrome

Doerbeck, V

Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis

Dorninger, L

Long-term outcome and MRI findings in children with acute cerebellitis

Duckwitz, H

Chronic valproate encephalopathy – an important differential diagnosis of cognitive decline within the scope of a valproate therapy. Case report and literature review

Ebbersmeyer, C

Characterization of endophenotypes in juvenile idiopathic generalized epilepsies by transcranial magnetic stimulation

Eberhardt, W

A 16 year-old patient presenting with Lambert-Eaton myasthenic syndrome

Eisert, E

Total cerebral blood flow during childhood and adolescence as assessed with phase-contrast imaging

Elger, C

Temporal lobe epilepsy with amygdala swelling and consecutive hippocampal sclerosis: Limbic or Rasmussen Encephalitis?

Hypomelanosis Ito and hemimegalencephaly

Elpers, C

Rare course of an intraspinal dermoid

Is neuritis nervi optici in children a predictor of multiple sclerosis in adulthood?

Elsas, J

Fetuin A: a new neuroprotective serum protein?

Engel, M

Encephalocraniocutaneous lipomatosis (ECCL) – a case report

Engelhardt, K von

Anti-NMDA Receptor Encephalitis in children

Englbrecht, M

Risk factors for progression to Multiple Sclerosis after Optic Neuritis

Ensslen, M

Immunoadsorption in refractory status epilepticus related to NMDAR-Encephalitis

Presurgical evaluation in refractory epilepsy in toddlers with depths electrodes

Ertl-Wagner, B

Short vertigo attacks in childhood: vestibular paroxysmia

Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis

Total cerebral blood flow during childhood and adolescence as assessed with phase-contrast imaging

Faldum, A

Analysis of risk factors for pediatric low-grade glioma patients after long term follow-up of the HIT-LGG 1996 trial

Falkenstein, F

Analysis of risk factors for pediatric low-grade glioma patients after long term follow-up of the HIT-LGG 1996 trial

Fauth, C

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Fiedler, B

Rare course of an intraspinal dermoid

Is neuritis nervi optici in children a predictor of multiple sclerosis in adulthood?

Neuroborreliosis as a chameleon – mimicking tuberculous meningitis

Filges, I

Mosaic ring chromosome 3 in a child with epilepsy and developmental delay

Fisch, B

Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis

Fischbach, H

Burdens of parents with epileptic children – Results of a study using a short-form of the German version of the Impact-on-Family-Scale

Frantz, M

Burdens of parents with epileptic children – Results of a study using a short-form of the German version of the Impact-on-Family-Scale

Freiberg, C

Pseudotumor cerebri after resection of pituitary adenoma

Freudenberg, L

Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia

Friebel, D

Hypocretin-level during therapy with intravenous immunglobulines in an early stage of narcolepsy with cataplexy in childhood

Fritzsch, D

Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?

Frosch, M

CNS vasculitis as early manifestation of polyarteritis nodosa

Gärtner, J

Pseudotumor cerebri after resection of pituitary adenoma

Array CGH in children and adolescents with developmental delay or intellectual disability: are there phenotypic clues to clinically relevant chromosomal microaberrations?

Mitochondrial Encephalopathies caused by defective mitochondrial translation

Geis, T

Perinatal cerebral infarction due to incontinentia pigmenti

Genthner, A

Characterization of endophenotypes in juvenile idiopathic generalized epilepsies by transcranial magnetic stimulation

Gerlach, S von

Successful treatment of progressive hypertrophic cardiomyopathy with heart transplantation and rhapamycine in an infant with LEOPARD syndrome due to a heterozygous mutation in the PTPN11-gene (Q510E)

Gerling, C

Subacute sclerosing panencephalitis

Gerull, R

Neuroleptic Malignant Syndrome due to Tetrabenazine in a Boy with a Subacute Extrapyramidal Disorder

Giehler, J

Subacute sclerosing panencephalitis

Girisch, W

The role of Cochrane reviews in child neurology: A systematic analysis

Giunta, C

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Gnekow, A

Analysis of risk factors for pediatric low-grade glioma patients after long term follow-up of the HIT-LGG 1996 trial

An opel-label, multi-center, expanded access study of RAD001 (Everolimus) in patients with TSC SEGA

Goebel, H

Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia

Goecke, T

Sudden bilateral sensorineural deafness in a 5 years old girl with blue sclerae, keratoconus, hypermobility of the joints and hyperelasticity of the skin with a mutation in the ZNF469 gene encoding for Brittle-Cornea-Syndrome

Goelz, R

Relationship between growth and psychomotor development of preterm children

Gold, R

Optical Coherence Tomography in idiopathic intracranial hypertension – first experiences

Gortner, L

The role of Cochrane reviews in child neurology: A systematic analysis

Melatonin does not influence sleep-deprivation electroencephalogram recordings in children

Gottschling, S

Melatonin does not influence sleep-deprivation electroencephalogram recordings in children

Gräber, S

Melatonin does not influence sleep-deprivation electroencephalogram recordings in children

Gralla, J

Neuroleptic Malignant Syndrome due to Tetrabenazine in a Boy with a Subacute Extrapyramidal Disorder

Granel, M

Long-term Outcome after Vegetative State due to Near-Drowning and Quality of Life of the Families

Grasshoff, U

Large interstitial duplication in the LARGE-gene in a patient with Walker-Warburg-syndrome.

Grenzebach, U

Is neuritis nervi optici in children a predictor of multiple sclerosis in adulthood?

Gressnich, M

Focal epilepsy caused by multiple cavernous hemangiomas and mental retardation – successful therapy and genetic cause (CCM3)

Gröschel, S

Stem cell transplantation (SCT) in metachromatic leukodystrophy (MLD) – results from 9 patients

Metachromatic Leukodystrophy – cerebral grey and white matter volume changes and clinical course

Lateralization of language pathways in children as assessed using fMRI-guided probabilistic tractography

Grotzer, M

Isolated spinal juvenile xanthogranuloma in an infant presenting as acute paraplegia

Gruber-Sedlmayr, U

Tick-borne encephalitis: four cases in young vaccinated children

CT Perfusion and CT Angiography in children and juvenile patients during an attack of migraine with aura

Chronic inflammatory bowel disease and cerebrovascular insults in a pediatric patient: a case report

Bannayan-Riley-Ruvalcaba-Syndrome – a rare differential diagnosis in children with macrocephaly

Gruender, S

Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis

Grunt, S

Macrocerebellum: not a clinical and neuroimaging entity

Neuroleptic Malignant Syndrome due to Tetrabenazine in a Boy with a Subacute Extrapyramidal Disorder

Grzmil, P

Array CGH in children and adolescents with developmental delay or intellectual disability: are there phenotypic clues to clinically relevant chromosomal microaberrations?

Hackenberg, A

Behavioural changes and unilateral movement disorder in 2 adolescents with Chorea Sydenham

Hager, S

Laterality, bimanual interference and short-term motor learning of fine motor movements in childhood and adolescence

Hahn, A

Ring chromosome 22 and neurofibromatosis type II: proof of two hit model for the loss of the NF2 gene in the development of meningioma

Characterization of endophenotypes in juvenile idiopathic generalized epilepsies by transcranial magnetic stimulation

Treatment of infantile Pompe s disease with enzyme replacement therapy in Germany and Austria

Prevalence of Antineuronal Antibodies in Children with Autoimmune Thyreoiditis and/or Encephalitis of Unclear Etiology

Successful treatment of progressive hypertrophic cardiomyopathy with heart transplantation and rhapamycine in an infant with LEOPARD syndrome due to a heterozygous mutation in the PTPN11-gene (Q510E)

Cerebral Thiamine-Transporter-Deficiency (SLC19A3) – A Rare But Treatable Cause Of An Acute Necrotizing Encephalopathy

Hahn, G

The pathogenesis and phenotype of children with microcephaly – Retrospective analysis and development of a microcephaly database

Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia

Hallermann, G

Pseudotumor cerebri after resection of pituitary adenoma

Hantel, T

Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?

Happle, R

A postzygotic activating AKT1 mutation in a discordant monozygotic twin with Proteus syndrome

Harder, A

Sleepless flies – Clinical and molecular genetic characterization of sleep disturbances in neurofibromatosis

Hartmann, H

Long-term outcome and MRI findings in children with acute cerebellitis

Fluctuating N IV paresis as presenting sign of a brain stem tumor: two pediatric cases

Hartung, R

Respiration and its correlation with motoric function in non-classic Pompe disease

Haslinger, V

Validity of the clinical neurological state and nerve conduction velocity in diagnosing diabetic peripheral neuropathy

Hauser, A

Burdens of parents with epileptic children – Results of a study using a short-form of the German version of the Impact-on-Family-Scale

Hauser, T

Lateralization of language pathways in children as assessed using fMRI-guided probabilistic tractography

Häusler, M

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Long-term outcome and MRI findings in children with acute cerebellitis

FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment

Fetuin A: a new neuroprotective serum protein?

Subacute sclerosing panencephalitis

Bannayan-Riley-Ruvalcaba-syndrom – an unusual differential diagnosis of dilatated Virchow-Robin spaces

Hehr, U

Perinatal cerebral infarction due to incontinentia pigmenti

Large interstitial duplication in the LARGE-gene in a patient with Walker-Warburg-syndrome.

Heinen, F

Short vertigo attacks in childhood: vestibular paroxysmia

Familial mutation in ACTA1 gene – clinical variability

Immunoadsorption in refractory status epilepticus related to NMDAR-Encephalitis

Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis

Total cerebral blood flow during childhood and adolescence as assessed with phase-contrast imaging

Development of an evidence- and consensus-based guideline for the diagnosis of fetal alcohol syndrome in Germany

Multiple sclerosis and periodic fever syndromes: Characterization of clinical symptoms

Presurgical evaluation in refractory epilepsy in toddlers with depths electrodes

Heitzer, E

Bannayan-Riley-Ruvalcaba-Syndrome – a rare differential diagnosis in children with macrocephaly

Helbig, I

Clinical characterization of myoclonic-astatic epilepsy

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Heller, R

Myasthenic symptoms: From initial presentation to diagnosis

Hennekam, R

Oral-Facial-Digital Syndrome Type VI: Delineation and Diagnostic Criteria

Hennermann, J

Treatment of infantile Pompe s disease with enzyme replacement therapy in Germany and Austria

Hennes, E

Long-term outcome and MRI findings in children with acute cerebellitis

Hentschel, R

Mowat-Wilson Syndrome, a rare genetic condition with intestinal and cerebral symptoms

Hernáiz Driever, P

Analysis of risk factors for pediatric low-grade glioma patients after long term follow-up of the HIT-LGG 1996 trial

An opel-label, multi-center, expanded access study of RAD001 (Everolimus) in patients with TSC SEGA

Laterality, bimanual interference and short-term motor learning of fine motor movements in childhood and adolescence

Herraiz Rocamora, J

Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity

Herrmann, M

Fetuin A: a new neuroprotective serum protein?

Hertzberg, C

An opel-label, multi-center, expanded access study of RAD001 (Everolimus) in patients with TSC SEGA

Heruth, M

Influence of antiepileptic treatment on bone metabolism

Herzog, A

Respiration and its correlation with motoric function in non-classic Pompe disease

Hessenauer, M

Long-term Outcome after Vegetative State due to Near-Drowning and Quality of Life of the Families

Ipsilateral Motor Control Without Mirror Movements?

Heußinger, N

Risk factors for progression to Multiple Sclerosis after Optic Neuritis

Pyruvate dehydrogenase deficiency: Novel PDHA1 mutation in a child with progressive encephalopathy

Hiener, U

Gastroenteritis associated encephalopathy with reversible splenial lesion: three cases

Hjalgrim, H

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Hoche, F

Novel CLCN1 mutation in a young male with Becker Myotonia and unique clinical phenotype

Ataxia Telangiectasia (AT) as a radiation sensitivity syndrom and limits of radiotherapeutic intervention

Hoeliner, I

Validity of the clinical neurological state and nerve conduction velocity in diagnosing diabetic peripheral neuropathy

Hoffjan, S

Ring chromosome 22 and neurofibromatosis type II: proof of two hit model for the loss of the NF2 gene in the development of meningioma

Hofmann, R

mRNA-expression patterns of Fas and its signalling cascade in Multiple Sclerosis (MS) and Experimental Autoimmune Encephalomyelitis (EAE)

Prevalence of Antineuronal Antibodies in Children with Autoimmune Thyreoiditis and/or Encephalitis of Unclear Etiology

Hofmann-Peters, A

Comorbidity of Epilepsy and early onset autism or Landau-Kleffner-Syndrome only?

Tonic eyelid movements in a patient with hypothalamic hamartoma

Hohlfeld, R

Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis

Höhn, T

Brown-Vialetto-Van Laere syndrome: A riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene

Holert, N

Valproate induced nocturnal enuresis – a seldom side effect?

Höliner, I

Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities

Holzinger, D

CNS vasculitis as early manifestation of polyarteritis nodosa

Horn, D

The pathogenesis and phenotype of children with microcephaly (MC) – Establishment of a multi-center microcephaly database (Department of Child Neurology in Berlin 2000–2010)

Hornstein, S von

Analysis of risk factors for pediatric low-grade glioma patients after long term follow-up of the HIT-LGG 1996 trial

Hübner, C

A novel X-linked neurodegenerative disorder affecting the central, peripheral and autonomic nervous system

Huemer, M

Treatment of infantile Pompe s disease with enzyme replacement therapy in Germany and Austria

Huisman, T

Oral-Facial-Digital Syndrome Type VI: Delineation and Diagnostic Criteria

Macrocerebellum: not a clinical and neuroimaging entity

Bannayan-Riley-Ruvalcaba-Syndrom with progressive spinal epidural lipomatosis

Huppke, P

Pseudotumor cerebri after resection of pituitary adenoma

Long-term outcome and MRI findings in children with acute cerebellitis

i Dali, C

Metachromatic Leukodystrophy – cerebral grey and white matter volume changes and clinical course

Illsinger, S

Fluctuating N IV paresis as presenting sign of a brain stem tumor: two pediatric cases

Irnberger, E

Intranasal insulin may influence motor activities and behaviour in Phelan McDermid Syndrom

Isbrandt, D

KCNQ2(NMF134)-mutant mice as a model for severe neonatal epilepsy

Issa, L

Microcephaly and Effects of Cdk5rap2 Downregulation in Murine Embryonic Stem Cells

Jacobs, J

Long-term outcome and MRI findings in children with acute cerebellitis

Clinical characterization of myoclonic-astatic epilepsy

Jahn, K

Short vertigo attacks in childhood: vestibular paroxysmia

Jahnen-Dechent, W

Fetuin A: a new neuroprotective serum protein?

Janßen, G

An opel-label, multi-center, expanded access study of RAD001 (Everolimus) in patients with TSC SEGA

Jeibmann, A

Sleepless flies – Clinical and molecular genetic characterization of sleep disturbances in neurofibromatosis

Jenke, A

Influence of antiepileptic treatment on bone metabolism

Jorch, G

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Joseph, T

Successful treatment of progressive hypertrophic cardiomyopathy with heart transplantation and rhapamycine in an infant with LEOPARD syndrome due to a heterozygous mutation in the PTPN11-gene (Q510E)

Jung, N

Macrocerebellum: not a clinical and neuroimaging entity

Kaindl, A

The pathogenesis and phenotype of children with microcephaly – Retrospective analysis and development of a microcephaly database

The pathogenesis and phenotype of children with microcephaly (MC) – Establishment of a multi-center microcephaly database (Department of Child Neurology in Berlin 2000–2010)

Growth and psychomotor development of patients with Duchenne Muscular Dystrophy

Microcephaly and Effects of Cdk5rap2 Downregulation in Murine Embryonic Stem Cells

Kaiser, O

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Karabul, N

Respiration and its correlation with motoric function in non-classic Pompe disease

Karch, S

Encephalocraniocutaneous lipomatosis (ECCL) – a case report

Karenfort, M

Sudden bilateral sensorineural deafness in a 5 years old girl with blue sclerae, keratoconus, hypermobility of the joints and hyperelasticity of the skin with a mutation in the ZNF469 gene encoding for Brittle-Cornea-Syndrome

Myasthenia gravis in an 22 months-old girl – impressing improvement due to early adaequate therapy

An opel-label, multi-center, expanded access study of RAD001 (Everolimus) in patients with TSC SEGA

Influence of antiepileptic treatment on bone metabolism

Kehrer, C

Stem cell transplantation (SCT) in metachromatic leukodystrophy (MLD) – results from 9 patients

Metachromatic Leukodystrophy – cerebral grey and white matter volume changes and clinical course

Kieslich, M

Leucencephalopathy with intracranial calcifications and cysts as well as conjuctival and pharyngeal teleangiectasias: Labrune syndrome variant

Novel CLCN1 mutation in a young male with Becker Myotonia and unique clinical phenotype

A new de novo deletion 4q13.2q13.3 in a patient with mental retardation, growth retardation and various facial and skeletal dysmorphic features

Ataxia Telangiectasia (AT) as a radiation sensitivity syndrom and limits of radiotherapeutic intervention

Kilian, D

Statistical properties of the jNCL scoring system according to Kohlschütter (1988)

Kinder, S

Acetazolamide as treatment for GLUT1 deficiency syndrome?

Kinkeldey, A

Fetuin A: a new neuroprotective serum protein?

Kirsch, A

Long-term Outcome after Vegetative State due to Near-Drowning and Quality of Life of the Families

Kirschner, J

Manifestation of muscular dystrophy by Anoctamin-5 mutation in infancy

Klein, C

Do young adolescents with periodic ataxia due to GLUT-1 Deficiency profit from introduction of a modified Atkins Diet?

Klein, N

Array CGH in children and adolescents with developmental delay or intellectual disability: are there phenotypic clues to clinically relevant chromosomal microaberrations?

Kleiss, R

Clinical characterization of myoclonic-astatic epilepsy

Klitten, L

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Kluger, G

FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment

Clinical characterization of myoclonic-astatic epilepsy

Narrowing down the minimal critical region for epilepsy susceptibility in chromosome 5p

Oral-Facial-Digital Syndrome Type VI: Delineation and Diagnostic Criteria

Long-term Outcome after Vegetative State due to Near-Drowning and Quality of Life of the Families

3D-Television and the Risk of Seizures in Children

Visual diagnosis of Morbus Niemann Pick Typ C

Knöfler, R

Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia

Koch, J

Long-term outcome and MRI findings in children with acute cerebellitis

Koch, K

Minimal invasive fetoscopic closure of myelomeningocele – postoperative care and interdisciplinary disease-management

Koch, M

Peroneal nerve palsy pointing towards a cerebral disorder

Impaired Control of Respiration as Crucial Evidence for Pitt-Hopkins Syndrome

Koehler, U

Narrowing down the minimal critical region for epilepsy susceptibility in chromosome 5p

Koerte, I

Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis

Total cerebral blood flow during childhood and adolescence as assessed with phase-contrast imaging

Kohl, B

Pseudotumor cerebri in an 8 month old infant

Kohleis, K

Predictors of comorbid psychiatric disorders in children and adolescents with cerebral palsy. Impact on family burden and quality of life. Results of a multicenter study

Köhler, C

New mutation in TSC1-gene in a sporadic case with initially mild phenotype

Kohlhase, J

Sudden bilateral sensorineural deafness in a 5 years old girl with blue sclerae, keratoconus, hypermobility of the joints and hyperelasticity of the skin with a mutation in the ZNF469 gene encoding for Brittle-Cornea-Syndrome

Kohlschütter, A

Quantitative Brain Volumetric Analysis in Neuronal Ceroid Lipofuscinoses: A tool to precisely monitor disease progression

Statistical properties of the jNCL scoring system according to Kohlschütter (1988)

König, A

A postzygotic activating AKT1 mutation in a discordant monozygotic twin with Proteus syndrome

König, J

Nephronophthisis Registry

König, R

A new de novo deletion 4q13.2q13.3 in a patient with mental retardation, growth retardation and various facial and skeletal dysmorphic features

Konrad, M

Nephronophthisis Registry

Korinthenberg, R

Pseudotumor cerebri under prednisolone treatment for infantile spasms

Korn-Merker, E

Burdens of parents with epileptic children – Results of a study using a short-form of the German version of the Impact-on-Family-Scale

Comorbidity of Epilepsy and early onset autism or Landau-Kleffner-Syndrome only?

Tonic eyelid movements in a patient with hypothalamic hamartoma

Kortmann, R

Analysis of risk factors for pediatric low-grade glioma patients after long term follow-up of the HIT-LGG 1996 trial

Kotzaeridou, U

Encephalocraniocutaneous lipomatosis (ECCL) – a case report

Kovacevic-Preradovic, T

Symptomatic epilepsy in patient with Klippel-Trénauney-Weber Syndrome. Case report and review of the literature

Valproate induced nocturnal enuresis – a seldom side effect?

Kovanovic, D

Symptomatic epilepsy in patient with Klippel-Trénauney-Weber Syndrome. Case report and review of the literature

Koy, A

Brown-Vialetto-Van Laere syndrome: A riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene

Krabichler, B

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Krägeloh-Mann, I

Early left-hemispheric brain lesions: When is Language Comprehension Reorganized?

Relationship between growth and psychomotor development of preterm children

Stem cell transplantation (SCT) in metachromatic leukodystrophy (MLD) – results from 9 patients

Metachromatic Leukodystrophy – cerebral grey and white matter volume changes and clinical course

Krämer, N

Microcephaly and Effects of Cdk5rap2 Downregulation in Murine Embryonic Stem Cells

Kraus, V

Long-term outcome and MRI findings in children with acute cerebellitis

Kremens, B

A 16 year-old patient presenting with Lambert-Eaton myasthenic syndrome

Kreß, W

Familial mutation in ACTA1 gene – clinical variability

Kreth, FW

Presurgical evaluation in refractory epilepsy in toddlers with depths electrodes

Kropp, A

Characterization of endophenotypes in juvenile idiopathic generalized epilepsies by transcranial magnetic stimulation

Kubin, L

Early postnatal alcohol exposure (PAE) causes a partial loss of motoneurons (MNs) in the ventral part of the hypoglossal nucleus (XIIn) in rats

Kuczaty, S

Temporal lobe epilepsy with amygdala swelling and consecutive hippocampal sclerosis: Limbic or Rasmussen Encephalitis?

Hypomelanosis Ito and hemimegalencephaly

Kudernatsch, M

Hand function after disconnection of the primary somatosensory representation as a consequence of hemispherotomy

Ipsilateral Motor Control Without Mirror Movements?

Kümpfel, T

Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis

Kunkel, J

Controlled Hypothermia after cold water immersion – (more than) a therapeutic option?

Kurlemann, G

Rare course of an intraspinal dermoid

Nephronophthisis Registry

Is neuritis nervi optici in children a predictor of multiple sclerosis in adulthood?

Neuroborreliosis as a chameleon – mimicking tuberculous meningitis

Editorial

Charcot-Marie-Tooth type 2A2 and idiopathic intracranial hypertension coinciding in a 15-year old boy

Kuwertz-Bröking, E

Rare course of an intraspinal dermoid

Laass, M

Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia

Lablans, M

Nephronophthisis Registry

Laccone, F

Male Rett Syndrome – genetic diagnosis using oral mucosa swabs

Lahl, O

Long-term Outcome after Vegetative State due to Near-Drowning and Quality of Life of the Families

Lakshminarasimhan, M

Variants of Epidermal Nevus Syndromes with Hemimegalencephaly

Landgraf, M

Development of an evidence- and consensus-based guideline for the diagnosis of fetal alcohol syndrome in Germany

Langer, S

Attention deficit in patients with Noonan Syndrome (NS)

Langer, T

Influence of antiepileptic treatment on bone metabolism

Langhagen, T

Short vertigo attacks in childhood: vestibular paroxysmia

Längler, A

First discription of a Kearns-Sayre-like-syndrome with ragged red fibres and cerebral folate deficiency

Elevated alpha fetoprotein as indicator for ataxia with oculomotor apraxia type 2 (AOA2)

Laubender, R

Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis

Total cerebral blood flow during childhood and adolescence as assessed with phase-contrast imaging

Laufs, M

Leucencephalopathy with intracranial calcifications and cysts as well as conjuctival and pharyngeal teleangiectasias: Labrune syndrome variant

Novel CLCN1 mutation in a young male with Becker Myotonia and unique clinical phenotype

Ataxia Telangiectasia (AT) as a radiation sensitivity syndrom and limits of radiotherapeutic intervention

Lausch, E

Mowat-Wilson Syndrome, a rare genetic condition with intestinal and cerebral symptoms

Leiz, S

Gastroenteritis associated encephalopathy with reversible splenial lesion: three cases

Lidzba, K

Early left-hemispheric brain lesions: When is Language Comprehension Reorganized?

Lateralization of language pathways in children as assessed using fMRI-guided probabilistic tractography

Liebe, J

The pathogenesis and phenotype of children with microcephaly – Retrospective analysis and development of a microcephaly database

Liebner, T

Pseudotumor cerebri after resection of pituitary adenoma

Lindbichler, P

Bannayan-Riley-Ruvalcaba-Syndrome – a rare differential diagnosis in children with macrocephaly

Linden, T

Neuroborreliosis as a chameleon – mimicking tuberculous meningitis

Linder-Lucht, M

Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity

Lindhout, D

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Lindhurst, M

A postzygotic activating AKT1 mutation in a discordant monozygotic twin with Proteus syndrome

Link, A

Age dependent regulation of the neuroprotective factor activin in the mouse brain

Logeswaran, T

Successful treatment of progressive hypertrophic cardiomyopathy with heart transplantation and rhapamycine in an infant with LEOPARD syndrome due to a heterozygous mutation in the PTPN11-gene (Q510E)

Lohmeier, K

Sudden bilateral sensorineural deafness in a 5 years old girl with blue sclerae, keratoconus, hypermobility of the joints and hyperelasticity of the skin with a mutation in the ZNF469 gene encoding for Brittle-Cornea-Syndrome

Lohnstein, P

Sudden bilateral sensorineural deafness in a 5 years old girl with blue sclerae, keratoconus, hypermobility of the joints and hyperelasticity of the skin with a mutation in the ZNF469 gene encoding for Brittle-Cornea-Syndrome

Lohse, P

Multiple sclerosis and periodic fever syndromes: Characterization of clinical symptoms

Loll, J

Measuring quality of life in patients with life-limiting neuromuscular disorders: a pilot study using the Kidscreen-27- and KINDL-R-questionnaire

Losch, H

Multifocal Balo's concentric sclerosis in a 10-year-old German boy

Lucke, B

A novel X-linked neurodegenerative disorder affecting the central, peripheral and autonomic nervous system

Lücke, T

Neurocognitive testing of very low birth weight infants at an age of 4 years

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Optical Coherence Tomography in idiopathic intracranial hypertension – first experiences

New mutation in TSC1-gene in a sporadic case with initially mild phenotype

Lücking, K

Controlled Hypothermia after cold water immersion – (more than) a therapeutic option?

Lütschg, J

Central nervous system Lyme disease – Presentation of two cases

Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities

Validity of the clinical neurological state and nerve conduction velocity in diagnosing diabetic peripheral neuropathy

Lutz, S

Mutation in the Fukutin-Gene (FKTN) as cause of a mild congenital muscular dystrophy

Myasthenia gravis in an 22 months-old girl – impressing improvement due to early adaequate therapy

DELOS Phase III Study with Idebenone (Catena®) in Duchenne Muscular Dystrophy

A 16 year-old patient presenting with Lambert-Eaton myasthenic syndrome

Myasthenia gravis in young children and adolescents: clinical signs and treatment options

Machuta, K

Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis

Mainberger, F

Attention deficit in patients with Noonan Syndrome (NS)

Makhani, N

Hiccups, Vomiting and the Brain

Mall, V

Hypocretin-level during therapy with intravenous immunglobulines in an early stage of narcolepsy with cataplexy in childhood

Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia

Macrocerebellum: not a clinical and neuroimaging entity

Attention deficit in patients with Noonan Syndrome (NS)

Acetazolamide as treatment for GLUT1 deficiency syndrome?

Mallmann, R

Subacute sclerosing panencephalitis

Marquardt, T

Treatment of infantile Pompe s disease with enzyme replacement therapy in Germany and Austria

Massot Taurus, A

Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity

Maxonus, I

Intranasal insulin may influence motor activities and behaviour in Phelan McDermid Syndrom

May, T

Burdens of parents with epileptic children – Results of a study using a short-form of the German version of the Impact-on-Family-Scale

Mayatepek, E

Sudden bilateral sensorineural deafness in a 5 years old girl with blue sclerae, keratoconus, hypermobility of the joints and hyperelasticity of the skin with a mutation in the ZNF469 gene encoding for Brittle-Cornea-Syndrome

Brown-Vialetto-Van Laere syndrome: A riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene

Mayer, T

Valproate induced nocturnal enuresis – a seldom side effect?

Mayr, J

Pyruvate dehydrogenase deficiency: Novel PDHA1 mutation in a child with progressive encephalopathy

Meier, T

DELOS Phase III Study with Idebenone (Catena®) in Duchenne Muscular Dystrophy

Meitinger, T

Mitochondrial Encephalopathies caused by defective mitochondrial translation

Mellies, U

Myasthenic symptoms: From initial presentation to diagnosis

Mengel, E

Respiration and its correlation with motoric function in non-classic Pompe disease

Treatment of infantile Pompe s disease with enzyme replacement therapy in Germany and Austria

Merfort, J

Neuroborreliosis as a chameleon – mimicking tuberculous meningitis

Merkenschlager, A

Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?

Shaking the head without end – bobble-head doll syndrome in no-no direction

Meyer, S

The role of Cochrane reviews in child neurology: A systematic analysis

Melatonin does not influence sleep-deprivation electroencephalogram recordings in children

Middelhoff, C

Symptomatic Treatment of Tomaculous Polyneuropathy with Methylprednisolone

Milkereit, D

KCNQ2(NMF134)-mutant mice as a model for severe neonatal epilepsy

Miny, P

Mosaic ring chromosome 3 in a child with epilepsy and developmental delay

Möllers, M

Microcephaly – Capillary Malformation Syndrome: A new syndrome with severe epilepsy – the first german patient

Moll-Khosrawi, P

Statistical properties of the jNCL scoring system according to Kohlschütter (1988)

Moog, U

Encephalocraniocutaneous lipomatosis (ECCL) – a case report

Morellini, F

KCNQ2(NMF134)-mutant mice as a model for severe neonatal epilepsy

Morris-Rosendahl, D

Microcephaly – Capillary Malformation Syndrome: A new syndrome with severe epilepsy – the first german patient

Muehlhausen, C

Pseudotumor cerebri in an 8 month old infant

Mueller, A

Visual diagnosis of Morbus Niemann Pick Typ C

Mueller, G

Validity of the clinical neurological state and nerve conduction velocity in diagnosing diabetic peripheral neuropathy

Muhle, H

Clinical characterization of myoclonic-astatic epilepsy

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Müller, A

Long-term Outcome after Vegetative State due to Near-Drowning and Quality of Life of the Families

Müller, I

Stem cell transplantation (SCT) in metachromatic leukodystrophy (MLD) – results from 9 patients

Müller, M

Tick-borne encephalitis: four cases in young vaccinated children

CT Perfusion and CT Angiography in children and juvenile patients during an attack of migraine with aura

Müller-Felber, W

Familial mutation in ACTA1 gene – clinical variability

Multiple sclerosis and periodic fever syndromes: Characterization of clinical symptoms

Munteanu, M

Mutation in the Fukutin-Gene (FKTN) as cause of a mild congenital muscular dystrophy

Myasthenic symptoms: From initial presentation to diagnosis

Deletion 22q13 (Phelan-McDermid-Syndrom) in two children with delayed development of speech and muscular hypotonia

Münter, S

Symptomatic Treatment of Tomaculous Polyneuropathy with Methylprednisolone

Muntoni, F

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Møller, R

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Nagarajah, J

A 16 year-old patient presenting with Lambert-Eaton myasthenic syndrome

Nallinger, A

Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis

Nastulla, T

Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis

Nathrath, M

An opel-label, multi-center, expanded access study of RAD001 (Everolimus) in patients with TSC SEGA

Navarro-Ramirez, L

3D-Television and the Risk of Seizures in Children

Nebgen, S

Bannayan-Riley-Ruvalcaba-syndrom – an unusual differential diagnosis of dilatated Virchow-Robin spaces

Nelle, W

Epileptic seizures with mild gastroenteritis

Nestrasil, I

Quantitative Brain Volumetric Analysis in Neuronal Ceroid Lipofuscinoses: A tool to precisely monitor disease progression

Neu, A

KCNQ2(NMF134)-mutant mice as a model for severe neonatal epilepsy

Neubauer, B

Ring chromosome 22 and neurofibromatosis type II: proof of two hit model for the loss of the NF2 gene in the development of meningioma

Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity

Characterization of endophenotypes in juvenile idiopathic generalized epilepsies by transcranial magnetic stimulation

Prevalence of Antineuronal Antibodies in Children with Autoimmune Thyreoiditis and/or Encephalitis of Unclear Etiology

Cerebral Thiamine-Transporter-Deficiency (SLC19A3) – A Rare But Treatable Cause Of An Acute Necrotizing Encephalopathy

Neubert, G

Microcephaly and Effects of Cdk5rap2 Downregulation in Murine Embryonic Stem Cells

Neuhann, T

Narrowing down the minimal critical region for epilepsy susceptibility in chromosome 5p

Neumann, H

Neurocognitive testing of very low birth weight infants at an age of 4 years

Niederstadt, T

Is neuritis nervi optici in children a predictor of multiple sclerosis in adulthood?

CNS vasculitis as early manifestation of polyarteritis nodosa

Ninnemann, O

Microcephaly and Effects of Cdk5rap2 Downregulation in Murine Embryonic Stem Cells

Noachtar, S

Presurgical evaluation in refractory epilepsy in toddlers with depths electrodes

Nögel, S

Pyruvate dehydrogenase deficiency: Novel PDHA1 mutation in a child with progressive encephalopathy

Nolte, K

FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment

NolteBuchholtz, S

Measuring quality of life in patients with life-limiting neuromuscular disorders: a pilot study using the Kidscreen-27- and KINDL-R-questionnaire

Offner, F

Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities

Omran, H

Rare course of an intraspinal dermoid

Nephronophthisis Registry

CNS vasculitis as early manifestation of polyarteritis nodosa

Neuroborreliosis as a chameleon – mimicking tuberculous meningitis

Ondrouschek, M

Cerebral Thiamine-Transporter-Deficiency (SLC19A3) – A Rare But Treatable Cause Of An Acute Necrotizing Encephalopathy

Opladen, T

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment

Orlikowsky, T

FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment

Orosz, I

Relapsing hemiplegy and drop attacks in a patient with Sturge-Weber syndrome-like central nervous system abnormalities

Oschmann, P

mRNA-expression patterns of Fas and its signalling cascade in Multiple Sclerosis (MS) and Experimental Autoimmune Encephalomyelitis (EAE)

Otte, J

Symptomatic Treatment of Tomaculous Polyneuropathy with Methylprednisolone

Pargac, K

Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia

Acetazolamide as treatment for GLUT1 deficiency syndrome?

Penzien, J

An opel-label, multi-center, expanded access study of RAD001 (Everolimus) in patients with TSC SEGA

Peraud, A

Presurgical evaluation in refractory epilepsy in toddlers with depths electrodes

Perret, E

Neuroleptic Malignant Syndrome due to Tetrabenazine in a Boy with a Subacute Extrapyramidal Disorder

Peters, J

Gastroenteritis associated encephalopathy with reversible splenial lesion: three cases

Pfäfflin, M

Burdens of parents with epileptic children – Results of a study using a short-form of the German version of the Impact-on-Family-Scale

Pfleiderer, S

Multifocal Balo's concentric sclerosis in a 10-year-old German boy

Pieper, T

Narrowing down the minimal critical region for epilepsy susceptibility in chromosome 5p

Hand function after disconnection of the primary somatosensory representation as a consequence of hemispherotomy

Ipsilateral Motor Control Without Mirror Movements?

Pietsch, T

Analysis of risk factors for pediatric low-grade glioma patients after long term follow-up of the HIT-LGG 1996 trial

Pietz, J

Encephalocraniocutaneous lipomatosis (ECCL) – a case report

Anti-NMDA Receptor Encephalitis in children

Pilhatsch, A

Chronic inflammatory bowel disease and cerebrovascular insults in a pediatric patient: a case report

Pillekamp, F

Brown-Vialetto-Van Laere syndrome: A riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene

Pilz, M

Controlled Hypothermia after cold water immersion – (more than) a therapeutic option?

Pivarcsi, M

The pathogenesis and phenotype of children with microcephaly (MC) – Establishment of a multi-center microcephaly database (Department of Child Neurology in Berlin 2000–2010)

Plecko, B

Chronic inflammatory bowel disease and cerebrovascular insults in a pediatric patient: a case report

Plischke, H

3D-Television and the Risk of Seizures in Children

Poehler, V

Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity

Polster, T

Microcephaly – Capillary Malformation Syndrome: A new syndrome with severe epilepsy – the first german patient

Variants of Epidermal Nevus Syndromes with Hemimegalencephaly

Pomschar, A

Total cerebral blood flow during childhood and adolescence as assessed with phase-contrast imaging

Poretti, A

Oral-Facial-Digital Syndrome Type VI: Delineation and Diagnostic Criteria

Macrocerebellum: not a clinical and neuroimaging entity

Bannayan-Riley-Ruvalcaba-Syndrom with progressive spinal epidural lipomatosis

Porto, L

Leucencephalopathy with intracranial calcifications and cysts as well as conjuctival and pharyngeal teleangiectasias: Labrune syndrome variant

Preuss, M

Shaking the head without end – bobble-head doll syndrome in no-no direction

Prokisch, H

Mitochondrial Encephalopathies caused by defective mitochondrial translation

Prüfer, M

Hypocretin-level during therapy with intravenous immunglobulines in an early stage of narcolepsy with cataplexy in childhood

Püst, B

Pseudotumor cerebri in an 8 month old infant

Qirshi, M

Novel CLCN1 mutation in a young male with Becker Myotonia and unique clinical phenotype

Ataxia Telangiectasia (AT) as a radiation sensitivity syndrom and limits of radiotherapeutic intervention

Quijano-Roy, S

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Ranke, M

Relationship between growth and psychomotor development of preterm children

Reiser, M

Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis

Renneberg, A

Multifocal Balo's concentric sclerosis in a 10-year-old German boy

Rettinger, N

Short vertigo attacks in childhood: vestibular paroxysmia

Reuss, R

mRNA-expression patterns of Fas and its signalling cascade in Multiple Sclerosis (MS) and Experimental Autoimmune Encephalomyelitis (EAE)

Reutlinger, C

Clinical characterization of myoclonic-astatic epilepsy

Richter, M

Age dependent regulation of the neuroprotective factor activin in the mouse brain

Rieger-Fackeldey, E

Mowat-Wilson Syndrome, a rare genetic condition with intestinal and cerebral symptoms

Riess, A

Large interstitial duplication in the LARGE-gene in a patient with Walker-Warburg-syndrome.

Rieß, J

3D-Television and the Risk of Seizures in Children

Rittinger, O

Intranasal insulin may influence motor activities and behaviour in Phelan McDermid Syndrom

Rocamora Zuñiga, R

Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity

Rodemann, S

Relationship between growth and psychomotor development of preterm children

Rohrbach, M

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Rohrschneider, K

Encephalocraniocutaneous lipomatosis (ECCL) – a case report

Rompel, O

Risk factors for progression to Multiple Sclerosis after Optic Neuritis

Rosenbaum, T

Sleepless flies – Clinical and molecular genetic characterization of sleep disturbances in neurofibromatosis

Rosner, V

Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis

Rost, I

A new de novo deletion 4q13.2q13.3 in a patient with mental retardation, growth retardation and various facial and skeletal dysmorphic features

Rostásy, K

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Long-term outcome and MRI findings in children with acute cerebellitis

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Rübel, A

An opel-label, multi-center, expanded access study of RAD001 (Everolimus) in patients with TSC SEGA

Rückauer, K

Mowat-Wilson Syndrome, a rare genetic condition with intestinal and cerebral symptoms

Rückriegel, S

Laterality, bimanual interference and short-term motor learning of fine motor movements in childhood and adolescence

Rudnik-Schöneborn, S

FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment

Rupprich, K

A 16 year-old patient presenting with Lambert-Eaton myasthenic syndrome

Sander, J

Melatonin does not influence sleep-deprivation electroencephalogram recordings in children

Santer, R

Treatment of infantile Pompe s disease with enzyme replacement therapy in Germany and Austria

Sarrazin, E

Growth and psychomotor development of patients with Duchenne Muscular Dystrophy

Sassen, R

Temporal lobe epilepsy with amygdala swelling and consecutive hippocampal sclerosis: Limbic or Rasmussen Encephalitis?

Hypomelanosis Ito and hemimegalencephaly

Schaefer, S

Variants of Epidermal Nevus Syndromes with Hemimegalencephaly

Schaetz, K

Tonic eyelid movements in a patient with hypothalamic hamartoma

Schalamon, J

Chronic inflammatory bowel disease and cerebrovascular insults in a pediatric patient: a case report

Schara, U

Mutation in the Fukutin-Gene (FKTN) as cause of a mild congenital muscular dystrophy

Growth and psychomotor development of patients with Duchenne Muscular Dystrophy

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Myasthenia gravis in an 22 months-old girl – impressing improvement due to early adaequate therapy

DELOS Phase III Study with Idebenone (Catena®) in Duchenne Muscular Dystrophy

Myasthenic symptoms: From initial presentation to diagnosis

A 16 year-old patient presenting with Lambert-Eaton myasthenic syndrome

Myasthenia gravis in young children and adolescents: clinical signs and treatment options

Deletion 22q13 (Phelan-McDermid-Syndrom) in two children with delayed development of speech and muscular hypotonia

Schauer, U

Neurocognitive testing of very low birth weight infants at an age of 4 years

Scheer, I

Isolated spinal juvenile xanthogranuloma in an infant presenting as acute paraplegia

Bannayan-Riley-Ruvalcaba-Syndrom with progressive spinal epidural lipomatosis

Schenke, C

Risk factors for progression to Multiple Sclerosis after Optic Neuritis

Pyruvate dehydrogenase deficiency: Novel PDHA1 mutation in a child with progressive encephalopathy

Schetzek, S

Presurgical evaluation in refractory epilepsy in toddlers with depths electrodes

Schilling, S

Perinatal cerebral infarction due to incontinentia pigmenti

Controlled Hypothermia after cold water immersion – (more than) a therapeutic option?

Schlachter, K

Long-term outcome and MRI findings in children with acute cerebellitis

Schleede, L

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Schmid, H

Fluctuating N IV paresis as presenting sign of a brain stem tumor: two pediatric cases

Schmitt, B

FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment

Schmitt, O

Nephronophthisis Registry

Schmitt-Mechelke, T

Neonatal star gazing: tonic upward gaze as a manifestation of atypical non-ketotic hyperglycinemia

Acquired reversible pediatric parkinsonism of unknown origin – a case series

Schmitz, N

Novel CLCN1 mutation in a young male with Becker Myotonia and unique clinical phenotype

A new de novo deletion 4q13.2q13.3 in a patient with mental retardation, growth retardation and various facial and skeletal dysmorphic features

Ataxia Telangiectasia (AT) as a radiation sensitivity syndrom and limits of radiotherapeutic intervention

Schneider, S

Do young adolescents with periodic ataxia due to GLUT-1 Deficiency profit from introduction of a modified Atkins Diet?

Schneider-Gold, C

Myasthenic symptoms: From initial presentation to diagnosis

Schober, C

Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?

Shaking the head without end – bobble-head doll syndrome in no-no direction

Schober, H

Central nervous system Lyme disease – Presentation of two cases

Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities

Schoberer, M

FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment

Schoene-Bake, J

Temporal lobe epilepsy with amygdala swelling and consecutive hippocampal sclerosis: Limbic or Rasmussen Encephalitis?

Hypomelanosis Ito and hemimegalencephaly

Schönfelder, J

Hypocretin-level during therapy with intravenous immunglobulines in an early stage of narcolepsy with cataplexy in childhood

Schramm, J

Hypomelanosis Ito and hemimegalencephaly

Schreiber, G

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Schroeder, S

Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis

Schubert-Bast, S

Anti-NMDA Receptor Encephalitis in children

Schuelke, M

A novel X-linked neurodegenerative disorder affecting the central, peripheral and autonomic nervous system

Schulz, A

Quantitative Brain Volumetric Analysis in Neuronal Ceroid Lipofuscinoses: A tool to precisely monitor disease progression

Statistical properties of the jNCL scoring system according to Kohlschütter (1988)

Schwartz, O

Is neuritis nervi optici in children a predictor of multiple sclerosis in adulthood?

Charcot-Marie-Tooth type 2A2 and idiopathic intracranial hypertension coinciding in a 15-year old boy

Schwarz, C

Oral-Facial-Digital Syndrome Type VI: Delineation and Diagnostic Criteria

Schwarz, J

A novel X-linked neurodegenerative disorder affecting the central, peripheral and autonomic nervous system

Schwerin-Nagel, A

Bannayan-Riley-Ruvalcaba-Syndrome – a rare differential diagnosis in children with macrocephaly

Schwindt, W

Rare course of an intraspinal dermoid

Neuroborreliosis as a chameleon – mimicking tuberculous meningitis

Seelow, D

A novel X-linked neurodegenerative disorder affecting the central, peripheral and autonomic nervous system

Seick-Barbarini, D

Validity of the clinical neurological state and nerve conduction velocity in diagnosing diabetic peripheral neuropathy

Seiler, A

Microcephaly and Effects of Cdk5rap2 Downregulation in Murine Embryonic Stem Cells

Seitz, A

Encephalocraniocutaneous lipomatosis (ECCL) – a case report

Sellhaus, B

Fetuin A: a new neuroprotective serum protein?

Shadeen, G

Melatonin does not influence sleep-deprivation electroencephalogram recordings in children

Shamdeen, G

Myasthenia gravis in young children and adolescents: clinical signs and treatment options

Shapiro, E

Quantitative Brain Volumetric Analysis in Neuronal Ceroid Lipofuscinoses: A tool to precisely monitor disease progression

Shoukier, M

Ring chromosome 22 and neurofibromatosis type II: proof of two hit model for the loss of the NF2 gene in the development of meningioma

Array CGH in children and adolescents with developmental delay or intellectual disability: are there phenotypic clues to clinically relevant chromosomal microaberrations?

A familial epilepsy with behavioural features associated with a PCDH19 mutation

Siekmeyer, W

Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?

Simma, B

Central nervous system Lyme disease – Presentation of two cases

Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities

Validity of the clinical neurological state and nerve conduction velocity in diagnosing diabetic peripheral neuropathy

Skopnik, H

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Smitka, M

Measuring quality of life in patients with life-limiting neuromuscular disorders: a pilot study using the Kidscreen-27- and KINDL-R-questionnaire

Hypocretin-level during therapy with intravenous immunglobulines in an early stage of narcolepsy with cataplexy in childhood

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia

Treatment of infantile Pompe s disease with enzyme replacement therapy in Germany and Austria

Macrocerebellum: not a clinical and neuroimaging entity

Acetazolamide as treatment for GLUT1 deficiency syndrome?

Sorantin, E

CT Perfusion and CT Angiography in children and juvenile patients during an attack of migraine with aura

Speckmann, C

Mowat-Wilson Syndrome, a rare genetic condition with intestinal and cerebral symptoms

Sperl, W

Pyruvate dehydrogenase deficiency: Novel PDHA1 mutation in a child with progressive encephalopathy

Sperner, J

Do young adolescents with periodic ataxia due to GLUT-1 Deficiency profit from introduction of a modified Atkins Diet?

Spiczak, S von

Clinical characterization of myoclonic-astatic epilepsy

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Spiegler, J

Clinical characterization of myoclonic-astatic epilepsy

Do young adolescents with periodic ataxia due to GLUT-1 Deficiency profit from introduction of a modified Atkins Diet?

Stahn, V

Sleepless flies – Clinical and molecular genetic characterization of sleep disturbances in neurofibromatosis

Staudt, M

Narrowing down the minimal critical region for epilepsy susceptibility in chromosome 5p

Long-term Outcome after Vegetative State due to Near-Drowning and Quality of Life of the Families

3D-Television and the Risk of Seizures in Children

Visual diagnosis of Morbus Niemann Pick Typ C

Hand function after disconnection of the primary somatosensory representation as a consequence of hemispherotomy

Ipsilateral Motor Control Without Mirror Movements?

Steffinger, D

Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis

Total cerebral blood flow during childhood and adolescence as assessed with phase-contrast imaging

Stehling, F

Myasthenic symptoms: From initial presentation to diagnosis

Stehr, F

Networking strategies to fight a fatal children disease

Steiner, G

Clinical characterization of myoclonic-astatic epilepsy

Steinlin, M

Macrocerebellum: not a clinical and neuroimaging entity

Video documentation of a case of Dopa responsive Dystonia in early infancy: a rare but important diagnosis

Steinmann, B

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Stenzel, W

Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia

Stephan, S

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Stephani, U

Epileptic seizures with mild gastroenteritis

Clinical characterization of myoclonic-astatic epilepsy

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Stettner, G

Early postnatal alcohol exposure (PAE) causes a partial loss of motoneurons (MNs) in the ventral part of the hypoglossal nucleus (XIIn) in rats

Storck, M

Predictors of comorbid psychiatric disorders in children and adolescents with cerebral palsy. Impact on family burden and quality of life. Results of a multicenter study

Streckert, I

Subacute sclerosing panencephalitis

Strobl-Wildemann, G

Familial mutation in ACTA1 gene – clinical variability

Stroet, A

Optical Coherence Tomography in idiopathic intracranial hypertension – first experiences

Strozzi, S

Video documentation of a case of Dopa responsive Dystonia in early infancy: a rare but important diagnosis

Neuroleptic Malignant Syndrome due to Tetrabenazine in a Boy with a Subacute Extrapyramidal Disorder

Stuecklin, A

Hypomelanosis Ito and hemimegalencephaly

Stülpnagel, C von

Narrowing down the minimal critical region for epilepsy susceptibility in chromosome 5p

Long-term Outcome after Vegetative State due to Near-Drowning and Quality of Life of the Families

3D-Television and the Risk of Seizures in Children

Stupp, N

Is neuritis nervi optici in children a predictor of multiple sclerosis in adulthood?

Sutter, C

New mutation in TSC1-gene in a sporadic case with initially mild phenotype

Syrbe, S

Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?

Shaking the head without end – bobble-head doll syndrome in no-no direction

Tacke, U

Pseudotumor cerebri under prednisolone treatment for infantile spasms

Mowat-Wilson Syndrome, a rare genetic condition with intestinal and cerebral symptoms

Teig, N

Neurocognitive testing of very low birth weight infants at an age of 4 years

Theis, M

Novel CLCN1 mutation in a young male with Becker Myotonia and unique clinical phenotype

Ataxia Telangiectasia (AT) as a radiation sensitivity syndrom and limits of radiotherapeutic intervention

Thiels, C

New mutation in TSC1-gene in a sporadic case with initially mild phenotype

Thomas, T

mRNA-expression patterns of Fas and its signalling cascade in Multiple Sclerosis (MS) and Experimental Autoimmune Encephalomyelitis (EAE)

Thöny, B

Video documentation of a case of Dopa responsive Dystonia in early infancy: a rare but important diagnosis

Thyen, U

Relapsing hemiplegy and drop attacks in a patient with Sturge-Weber syndrome-like central nervous system abnormalities

Tibussek, D

Oral-Facial-Digital Syndrome Type VI: Delineation and Diagnostic Criteria

Tietz, S

mRNA-expression patterns of Fas and its signalling cascade in Multiple Sclerosis (MS) and Experimental Autoimmune Encephalomyelitis (EAE)

Tinschert, S

The pathogenesis and phenotype of children with microcephaly – Retrospective analysis and development of a microcephaly database

Toelle, S

Macrocerebellum: not a clinical and neuroimaging entity

Bannayan-Riley-Ruvalcaba-Syndrom with progressive spinal epidural lipomatosis

Trippe, H

Mutation in the Fukutin-Gene (FKTN) as cause of a mild congenital muscular dystrophy

Myasthenic symptoms: From initial presentation to diagnosis

Myasthenia gravis in young children and adolescents: clinical signs and treatment options

Deletion 22q13 (Phelan-McDermid-Syndrom) in two children with delayed development of speech and muscular hypotonia

Trollmann, R

Risk factors for progression to Multiple Sclerosis after Optic Neuritis

Age dependent regulation of the neuroprotective factor activin in the mouse brain

Pyruvate dehydrogenase deficiency: Novel PDHA1 mutation in a child with progressive encephalopathy

Tschumi, S

Neuroleptic Malignant Syndrome due to Tetrabenazine in a Boy with a Subacute Extrapyramidal Disorder

Uhrig, S

Bannayan-Riley-Ruvalcaba-Syndrome – a rare differential diagnosis in children with macrocephaly

Ulmer, H

Long-term outcome and MRI findings in children with acute cerebellitis

Urbach, H

Temporal lobe epilepsy with amygdala swelling and consecutive hippocampal sclerosis: Limbic or Rasmussen Encephalitis?

Hypomelanosis Ito and hemimegalencephaly

Valente, E

Oral-Facial-Digital Syndrome Type VI: Delineation and Diagnostic Criteria

van Baalen, A

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Long-term outcome and MRI findings in children with acute cerebellitis

Epileptic seizures with mild gastroenteritis

FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment

van Kempen, M

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

van Riesen, A

A novel X-linked neurodegenerative disorder affecting the central, peripheral and autonomic nervous system

Verhoeven, N

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Vieker, S

First discription of a Kearns-Sayre-like-syndrome with ragged red fibres and cerebral folate deficiency

Elevated alpha fetoprotein as indicator for ataxia with oculomotor apraxia type 2 (AOA2)

Vietzke, D

Sudden bilateral sensorineural deafness in a 5 years old girl with blue sclerae, keratoconus, hypermobility of the joints and hyperelasticity of the skin with a mutation in the ZNF469 gene encoding for Brittle-Cornea-Syndrome

Vivanco Hidalgo, R

Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity

Vlaho, S

Novel CLCN1 mutation in a young male with Becker Myotonia and unique clinical phenotype

Ataxia Telangiectasia (AT) as a radiation sensitivity syndrom and limits of radiotherapeutic intervention

Volgin, D

Early postnatal alcohol exposure (PAE) causes a partial loss of motoneurons (MNs) in the ventral part of the hypoglossal nucleus (XIIn) in rats

Vollmar, C

Presurgical evaluation in refractory epilepsy in toddlers with depths electrodes

Vry, J

Manifestation of muscular dystrophy by Anoctamin-5 mutation in infancy

Wagner, K

Bannayan-Riley-Ruvalcaba-Syndrome – a rare differential diagnosis in children with macrocephaly

Wagner, M

Visual diagnosis of Morbus Niemann Pick Typ C

Warmuth-Metz, M

Analysis of risk factors for pediatric low-grade glioma patients after long term follow-up of the HIT-LGG 1996 trial

Waterham, H

Brown-Vialetto-Van Laere syndrome: A riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene

Weber, G

Subacute sclerosing panencephalitis

Weber, L

Immunoadsorption in refractory status epilepticus related to NMDAR-Encephalitis

Weber, P

Isolated neonatal bilateral palsy of the n. radialis; case report and review of the literature

Wegendt, C

Microcephaly – Capillary Malformation Syndrome: A new syndrome with severe epilepsy – the first german patient

Wegener, A

Chronic valproate encephalopathy – an important differential diagnosis of cognitive decline within the scope of a valproate therapy. Case report and literature review

Wegjan, E

Chronic valproate encephalopathy – an important differential diagnosis of cognitive decline within the scope of a valproate therapy. Case report and literature review

Weigt-Usinger, K

Neurocognitive testing of very low birth weight infants at an age of 4 years

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Optical Coherence Tomography in idiopathic intracranial hypertension – first experiences

New mutation in TSC1-gene in a sporadic case with initially mild phenotype

Weimer, W

Charcot-Marie-Tooth type 2A2 and idiopathic intracranial hypertension coinciding in a 15-year old boy

Weis, J

FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment

Fetuin A: a new neuroprotective serum protein?

Weise, S

Neuroborreliosis without Neurology?!

Focal epilepsy caused by multiple cavernous hemangiomas and mental retardation – successful therapy and genetic cause (CCM3)

Chronic valproate encephalopathy – an important differential diagnosis of cognitive decline within the scope of a valproate therapy. Case report and literature review

Weitkämper, A

Neurocognitive testing of very low birth weight infants at an age of 4 years

Welcker, S

Characterization of endophenotypes in juvenile idiopathic generalized epilepsies by transcranial magnetic stimulation

Wiater, A

Sleepless flies – Clinical and molecular genetic characterization of sleep disturbances in neurofibromatosis

Wieczorek, D

Impaired Control of Respiration as Crucial Evidence for Pitt-Hopkins Syndrome

Deletion 22q13 (Phelan-McDermid-Syndrom) in two children with delayed development of speech and muscular hypotonia

Wiesmann, M

Bannayan-Riley-Ruvalcaba-syndrom – an unusual differential diagnosis of dilatated Virchow-Robin spaces

Wilichowski, E

Mitochondrial Encephalopathies caused by defective mitochondrial translation

Wilke, M

Early left-hemispheric brain lesions: When is Language Comprehension Reorganized?

Metachromatic Leukodystrophy – cerebral grey and white matter volume changes and clinical course

Lateralization of language pathways in children as assessed using fMRI-guided probabilistic tractography

Wilken, B

An opel-label, multi-center, expanded access study of RAD001 (Everolimus) in patients with TSC SEGA

Wille, D

Isolated spinal juvenile xanthogranuloma in an infant presenting as acute paraplegia

Behavioural changes and unilateral movement disorder in 2 adolescents with Chorea Sydenham

Willhelm, C

The role of Cochrane reviews in child neurology: A systematic analysis

Witt, O

An opel-label, multi-center, expanded access study of RAD001 (Everolimus) in patients with TSC SEGA

Woermann, F

Variants of Epidermal Nevus Syndromes with Hemimegalencephaly

Wolf, N

Leukoencephalopathy with metaphyseal chondrodysplasia

Wolff, M

Clinical characterization of myoclonic-astatic epilepsy

Wörnle, M

Immunoadsorption in refractory status epilepticus related to NMDAR-Encephalitis

Wortmann, S

First discription of a Kearns-Sayre-like-syndrome with ragged red fibres and cerebral folate deficiency

Wüller, D

Vena-Galeni-Malformation – What does the stethoscope has to look on the head?

Wunsch, R

Peroneal nerve palsy pointing towards a cerebral disorder

Wygoda, S

Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?

Young, P

Charcot-Marie-Tooth type 2A2 and idiopathic intracranial hypertension coinciding in a 15-year old boy

Zanier, U

Validity of the clinical neurological state and nerve conduction velocity in diagnosing diabetic peripheral neuropathy

Zebedin, D

CT Perfusion and CT Angiography in children and juvenile patients during an attack of migraine with aura

Zehle, K

Comorbidity of Epilepsy and early onset autism or Landau-Kleffner-Syndrome only?

Zenker, M

Successful treatment of progressive hypertrophic cardiomyopathy with heart transplantation and rhapamycine in an infant with LEOPARD syndrome due to a heterozygous mutation in the PTPN11-gene (Q510E)

Zenz, W

Tick-borne encephalitis: four cases in young vaccinated children

Zerres, K

Bannayan-Riley-Ruvalcaba-syndrom – an unusual differential diagnosis of dilatated Virchow-Robin spaces

Zinck, D

First discription of a Kearns-Sayre-like-syndrome with ragged red fibres and cerebral folate deficiency

Elevated alpha fetoprotein as indicator for ataxia with oculomotor apraxia type 2 (AOA2)

Zirn, B

Ring chromosome 22 and neurofibromatosis type II: proof of two hit model for the loss of the NF2 gene in the development of meningioma

Array CGH in children and adolescents with developmental delay or intellectual disability: are there phenotypic clues to clinically relevant chromosomal microaberrations?

Zoll, B

Array CGH in children and adolescents with developmental delay or intellectual disability: are there phenotypic clues to clinically relevant chromosomal microaberrations?

Zotter, S

Long-term outcome and MRI findings in children with acute cerebellitis

Zschocke, J

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Zsoter, A

Hand function after disconnection of the primary somatosensory representation as a consequence of hemispherotomy

Zwiener, I

Analysis of risk factors for pediatric low-grade glioma patients after long term follow-up of the HIT-LGG 1996 trial

Zwirner, A

A novel X-linked neurodegenerative disorder affecting the central, peripheral and autonomic nervous system

Ückert, F

Nephronophthisis Registry