Abstracts of the 33rd Annual Meeting – of the Society of Neuropediatrics – (Gesellschaft für Neuropädiatrie)

Aarab, S.

The 22q11 deletion syndrome poses a multidisciplinary challenge for pediatricians and child psychiatrists as shown by a case report

Abu-Tair, T.

PVL – A differentiation of various classifications

Akkurt, I.

Symptomatic west syndrome in neonatal diabetes and developmental delay (DEND-syndrome)?

Aksu, F.

Gait disturbance as a first sign of SSPE in early infancy

Albrecht, B.

Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K)

Albrecht, U.

3-Heptanone in exhaled breath gas of patients with propionic acidemia and therapy with valproate

Urea cycle defects: Changes of amino acid CSF/plasma-ratios

Allmendinger, A.

Levetiracetam in neonatal seizures

Altenmüller, D. M.

Factors influencing surgical outcome in patients with focal cortical dysplasia

Altenmüller, S.

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Amann, A.

3-Heptanone in exhaled breath gas of patients with propionic acidemia and therapy with valproate

Andres, O.

3-methylglutaconic aciduria in mitochondrial encepahlopathy: 2 case reports

Arnold, Y.

Vagus nerve stimulation and heart rate – the influence of vagus nerve stimulation output current on heart rate

Arslan, I.

Menkes-Syndrome: Delayed diagnosis because of misinterpretation as battered child syndrome in 2 of 3 children in 2006

Assmann, B.

Successfull therapy with Rituximab in an adolescent patient with severe multiple sclerosis

Auer, M.

Dextromethorphan an „old“ drug to protect the newborn brain against perinatal injury?

Baccin, C. E.

Sinus Pericranii: Diagnostic and therapeutic considerations

Bachmaier, N.

Loss of vertical gaze – the Parinaud syndrome

Baethmann, M.

Clinical and behavioural phenotype in a contiguous gene deletion syndrome at Xp22.3

Barthel, M.

Distal phalanx necrosis after intra-arterial injection of phenobarbital during treatment of subtle generalized convulsive status epilepticus

Bartmann, P.

Hemimegalencephaly – long-term follow up after functional hemispherectomy

Cerebrospinal fluid obstruction and CSF malresorption: Analysis of specific CSF biomarkers indicative for growth factor- and fibrosis- related CSF malabsorption in neonatal hydrocephalus

Bartsch, O.

Tuberous Sclerosis with deletion on chromosome 9q and TSC-2-like brain dysplasia but TSC 1- like outcome: a case report

Bast, T.

Combined EEG and MEG analysis of early tactile evoked activity in patients with focal epilepsies

Levetiracetam in neonatal seizures

Factors influencing surgical outcome in patients with focal cortical dysplasia

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Effects of signal-to-noise ratio and averaging in non-invasive source localization of interictal EEG spikes

Late diagnosis of pyridoxal- phosphate depending epilepsy: Case report of a 5 year old boy

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Efficacy of interstitial radiosurgery in the treatment of pharmacoresistant gelastic epilepsy due to hypothalamic hamartomas

Bauer, A.

Monosymptomatic rheumatic fever – Chorea Sydenham

Bauer, K.

Effect of early intervention on infantile postural asymmetry: a prospective 2 years follow-up

Baumgartner, S.

Therapy with ACTH versus pulsatile corticoid – retrospective analysis of efficacy in treatment of infantile epilepsy syndromes

Clinical experience using a rapid loading dose of levetiracetam in childhood epilepsy

Baumgärtner, U.

Combined EEG and MEG analysis of early tactile evoked activity in patients with focal epilepsies

Baumgartner Sigl, S.

Urea cycle defects: Changes of amino acid CSF/plasma-ratios

Baz Bartels, M.

Cognitive long- term outcomes after acute lymphoblastic leukaemia in childhood

Does valproic acid cause cardiac arrhythmias, in particular QT-prolongations, as possible SUDEP risk factor?

Bilateral decompressive craniectomy in a predominantly hypoxic brain damage

Retrobulbar pain, diplopia and exophthalmus as manifestations of an isolated ocular myositis in a 15 year old boy

Posterior Reversible Encephalopathy Syndrome (PRES) in children – a single-institution retrosprective study

Primary pseudotumor cerebri in association with obesity – a rare differential diagnosis even in childhood

Behnke-Mursch, J.

The evolution of shunt-technology

Bendl, C.

Valproic Acid associated encephalopathy –19 new cases in Germany from 1994 to 2003– a side effect associated to VPA-therapy not only in young children

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Bentele, K. H. P.

Partial trisomy 5p and deletion of the 1p region causes severe psychomotor delay, refractory epilepsy and cleft lip and palate in a 10-year old girl – a long way to diagnosis

Ptosis, microcephaly and delayed motor development as main clinical manifestations in a female patient with chromosome 18p deletion-syndrome

Bentfeld, M.

Symptomatic west syndrome in neonatal diabetes and developmental delay (DEND-syndrome)?

Bercker, S.

Neurodegeneration in newborn rats following general anesthesia

Bergmann, H.

Effect of early intervention on infantile postural asymmetry: a prospective 2 years follow-up

Bergmann, M.

Therapy resistant epilepsia partialis continua as leading symptom of Alpers disease

Bernert, G.

Double Trouble: A clinical, molecular genetic mixed type of FSHD and Selenoprotein N rigid spine syndrome as a „new“ neuromuscular disease

Bernhard, M. K.

Ophthalmological examination after a first seizure in paediatric patients are of low diagnostic value

Does barefoot walking alter the manifestation of idiopathic toe walking? – Low prevalence among the children slum population of Dhaka (Bangladesh)

Value and cost-benefit analysis of in-patient diagnosis of developmental retardation

Bert, B.

Neurodegeneration in newborn rats following general anesthesia

Bertini, E.

Frequency, Genotypic and Phenotypic Spectrum of Pelizaeus Merzbacher-like Disease caused by GJA12 Mutations

Berweck, S.

Reorganization in congenital hemiparesis: fMRI activation of ipsilateral basal ganglia during paretic hand movement

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a fMRI study

Intracortical inhibition in patients suffering from congenital hemiparesis

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

Integrity of the corticospinal system in children with bilateral cerebral palsy and periventricular leukomalacia: A transcranial magnetic stimulation study

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a TMS study

Formation of antibodies against botulinum toxin B after treatment of drooling in two children with cerebral palsy

Feasibility and first results of a binational, bicenter trial of locomotor therapy with a driven gait orthosis in children with central gait impairment

Bittigau, P.

Cannabinoids enhance the susceptibility of the immature brain to ethanol neurotoxicity

Neurodegeneration in newborn rats following general anesthesia

Bittner, R. E.

Double Trouble: A clinical, molecular genetic mixed type of FSHD and Selenoprotein N rigid spine syndrome as a „new“ neuromuscular disease

Blankenburg, M.

Gait disturbance as a first sign of SSPE in early infancy

Blanz, B.

Elective mutism, generalized seizures, developmental delay, mild mental retardation, dysmorphic features and renal dystopia in a 13-year-old boy – a case report

The 22q11 deletion syndrome poses a multidisciplinary challenge for pediatricians and child psychiatrists as shown by a case report

Blaschek, A.

Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option?

Blaschtikowitz, H.

Developmental testing in early infancy: aspects of stability and change in German preterm born infants and other biological high risk infants

Blaum, M.

Successful continuous lumbar intrathecal interferon alpha treatment in SSPE

Blümcke, I.

Histologic and molecular-genetic aspects of tuberous sclerosis complex

Boda, V.

Cognitive long- term outcomes after acute lymphoblastic leukaemia in childhood

Does valproic acid cause cardiac arrhythmias, in particular QT-prolongations, as possible SUDEP risk factor?

Bilateral decompressive craniectomy in a predominantly hypoxic brain damage

Retrobulbar pain, diplopia and exophthalmus as manifestations of an isolated ocular myositis in a 15 year old boy

Posterior Reversible Encephalopathy Syndrome (PRES) in children – a single-institution retrosprective study

Primary pseudotumor cerebri in association with obesity – a rare differential diagnosis even in childhood

Boespflug-Tanguy, O.

Frequency, Genotypic and Phenotypic Spectrum of Pelizaeus Merzbacher-like Disease caused by GJA12 Mutations

Boltshauser, E.

Pontine involvement as an imaging feature of severe hypoxic-ischemic encephalopathy in the term neonate

Failure of decussation of important pathways demonstrated by MR tractography in Joubert syndrome

Bonakdar, S.

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Efficacy of interstitial radiosurgery in the treatment of pharmacoresistant gelastic epilepsy due to hypothalamic hamartomas

Bönnemann, C.

Ubiquitin-Proteasome pathway alteration in distal myopathy due to a mutation in a novel kelch protein

Boor, R.

Combined EEG and MEG analysis of early tactile evoked activity in patients with focal epilepsies

Boppel, T.

Effects of signal-to-noise ratio and averaging in non-invasive source localization of interictal EEG spikes

Borell-Kost, S.

Developmental outcome of children conceived by ICSI at 5 years of age

Borggräfe, I.

Feasibility and first results of a binational, bicenter trial of locomotor therapy with a driven gait orthosis in children with central gait impairment

Borusiak, P.

Absence epilepsy and BECTS: just accident or genetics?

Bosch, F.

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Boscherini, D.

Clinical manifestations of benign tectal glioma in children and adolescents

Bougioukou, A.

Alexithymia in children, is it a brain disorder?

Brehmer, U.

Pontine involvement as an imaging feature of severe hypoxic-ischemic encephalopathy in the term neonate

Breuer, U.

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

Brocke, K. S.

Magnetic resonance imaging of skeletal muscles reveals a distinct pattern of muscle involvement in a family with congenital myopathy caused by a RYR1 mutation

Brockmann, K.

Treatment of epilepsy in patients with Rett syndrome

Leukoencephalopathy with brain stem and spinal cord involvement and elevated white matter lactate (LBSL): Serial proton MRS and DTI of a child over a period of 6 years

Frequency, Genotypic and Phenotypic Spectrum of Pelizaeus Merzbacher-like Disease caused by GJA12 Mutations

Brodbeck, V.

Intracortical inhibition in patients suffering from congenital hemiparesis

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a TMS study

Brückner, H.

Zonisamide in refractory epilepsies of childood and adolescence

Bruning, N.

Neurophysiological correlates of relatively enhanced local visual search in healthy and autistic adolescents

Bührer, C.

Neurodegeneration in newborn rats following general anesthesia

Burlina, A.

Frequency, Genotypic and Phenotypic Spectrum of Pelizaeus Merzbacher-like Disease caused by GJA12 Mutations

Busch, V.

Assessment of the respiratory center output in children with neuromuscular diseases

Büsing, D.

Valproic Acid associated encephalopathy –19 new cases in Germany from 1994 to 2003– a side effect associated to VPA-therapy not only in young children

Bußmann, C.

Levetiracetam in neonatal seizures

Calaminus, G.

Quality of life (QoL) in childhood craniopharyngioma – current status of the prospective multicenter study KRANIOPHARYNGEOM 2000 and results of a retrospective study on 185 long-term survivors

First randomized multicenter study in patients with childhood craniopharyngioma analyzing the appropriate time point of irradiation after incomplete resection – study design of KRANIOPHARYNGEOM 2007

Cirak, S.

Ubiquitin-Proteasome pathway alteration in distal myopathy due to a mutation in a novel kelch protein

Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K)

Collmann, H.

X-linked hydrocephalus: Another family with a novel mutation in the L1CAM-gene

Idiopathic intracranial hypertension – a review over 16 cases in childhood

Combes, P.

Frequency, Genotypic and Phenotypic Spectrum of Pelizaeus Merzbacher-like Disease caused by GJA12 Mutations

Cordes, J.

Atypical presentations of herpes simplex virus encephalitis

Cortesi, C.

Clinical manifestations of benign tectal glioma in children and adolescents

Courage, C.

An optimized scheme of motor learning

Czekalla, J.

Transition from immediate-release methylphenidate (IR-MPH) to extended-release methylphenidate (Oros®-MPH, Concerta®) is associated with an improvement in quality of life in patients with ADHD – results from an open label naturalistic study

Däublin, G.

Therapy resistant epilepsia partialis continua as leading symptom of Alpers disease

Daumer-Haas, C.

Clinical and behavioural phenotype in a contiguous gene deletion syndrome at Xp22.3

Debus, O.

Herpes Simplex Encephalitis: Progressive MRI-deterioration despite clinical stabilization with Acyclovir

Dechent, P.

Leukoencephalopathy with brain stem and spinal cord involvement and elevated white matter lactate (LBSL): Serial proton MRS and DTI of a child over a period of 6 years

Deeg, K. H.

Hydrocephalus – Sonographic differential diagnosis and Dopplersonographic flow measurements

Deimling, F.

Efficacy of interstitial radiosurgery in the treatment of pharmacoresistant gelastic epilepsy due to hypothalamic hamartomas

Deimling, F. von

Ubiquitin-Proteasome pathway alteration in distal myopathy due to a mutation in a novel kelch protein

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Demel, H.

Video and EEG documentation of seizures induced by showering in 2 photosensitive patients

Dewitz, R.

Cognitive long- term outcomes after acute lymphoblastic leukaemia in childhood

Dieckhöfer, A.

Neurological manifestations of EBV infection: a heterogeneous disease entity

Diekmann, S.

Frequency, Genotypic and Phenotypic Spectrum of Pelizaeus Merzbacher-like Disease caused by GJA12 Mutations

Dierks, T.

Clinical and molecular characterization of patients with multiple sulfatase deficiency

Dietz, B.

Gait disturbance as a first sign of SSPE in early infancy

Distelmaier, F.

Seasonal clustering of prepubertal idiopathic intracranial hypertension

Dittrich, S.

Cognitive long- term outcomes after acute lymphoblastic leukaemia in childhood

Does valproic acid cause cardiac arrhythmias, in particular QT-prolongations, as possible SUDEP risk factor?

Bilateral decompressive craniectomy in a predominantly hypoxic brain damage

Retrobulbar pain, diplopia and exophthalmus as manifestations of an isolated ocular myositis in a 15 year old boy

Posterior Reversible Encephalopathy Syndrome (PRES) in children – a single-institution retrosprective study

Primary pseudotumor cerebri in association with obesity – a rare differential diagnosis even in childhood

Dreha-Kulaczewski, S.

Leukoencephalopathy with brain stem and spinal cord involvement and elevated white matter lactate (LBSL): Serial proton MRS and DTI of a child over a period of 6 years

Dushe, T.

Video and EEG documentation of seizures induced by showering in 2 photosensitive patients

Ebenbichler, C.

Effect of valproic acid treatment on body composition, leptin and soluble leptin receptor in epileptic children

Eberhardt, F.

KCNQ3 and KCNQ2 mutations contribute to rare and common forms of idiopathic epilepsy

Ebner, A.

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Elger, C.

Efficacy of interstitial radiosurgery in the treatment of pharmacoresistant gelastic epilepsy due to hypothalamic hamartomas

Elger, C. E.

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Elkemann, U.

Cognitive outcome of postpubertal patients with benign partial epilepsy with centrotemporal sharp waves (type Rolando) in childhood and adolescence

Ellard, S.

Symptomatic west syndrome in neonatal diabetes and developmental delay (DEND-syndrome)?

Emser, A.

High rates of early relapses after complete resection and early tumor progressions after incomplete resection of childhood craniopharyngioma – update after three years of prospective evaluation in KRANIOPHARYNGEOM 2000

History and symptoms at primary diagnosis of childhood craniopharyngioma in 311 patients

Melatonin treatment in obese patients with childhood craniopharyngioma and increased daytime sleepiness

First randomized multicenter study in patients with childhood craniopharyngioma analyzing the appropriate time point of irradiation after incomplete resection – study design of KRANIOPHARYNGEOM 2007

Engelskirchen, R.

Can 18FDG-PET detect malignant transformation of neurofibromas in patients with neurofibromatosis type I?

Engl, J.

Effect of valproic acid treatment on body composition, leptin and soluble leptin receptor in epileptic children

Erhart, S.

3-Heptanone in exhaled breath gas of patients with propionic acidemia and therapy with valproate

Ernst, J. P.

Febrile seizures, loss of consciousness, EEG-patterns with focal and diffuse slowing, epilepsy in the family history – no epilepsy?

Zonisamide in refractory epilepsies of childood and adolescence

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Efficacy of interstitial radiosurgery in the treatment of pharmacoresistant gelastic epilepsy due to hypothalamic hamartomas

IQ-decrease by antiepileptic therapy

Esmaeili, A.

Does valproic acid cause cardiac arrhythmias, in particular QT-prolongations, as possible SUDEP risk factor?

Esslinger, P.

Relevance of abdominal fluid for the assessment of ventriculoperitoneal shunt function in children

Everts, R.

Reactivation of bilateral cognitive networks after stroke in childhood

Faggin, R.

Clinical manifestations of benign tectal glioma in children and adolescents

Fahnenstich, H.

Mismatch detection: an auditory event-related study to detect differences in pre-attentive and learning capability of fullterm and preterm newborns

Fahrbach, J.

Zonisamide in refractory epilepsies of childood and adolescence

Faist, M.

Integrity of the corticospinal system in children with bilateral cerebral palsy and periventricular leukomalacia: A transcranial magnetic stimulation study

Faldum, A.

High rates of early relapses after complete resection and early tumor progressions after incomplete resection of childhood craniopharyngioma – update after three years of prospective evaluation in KRANIOPHARYNGEOM 2000

History and symptoms at primary diagnosis of childhood craniopharyngioma in 311 patients

Melatonin treatment in obese patients with childhood craniopharyngioma and increased daytime sleepiness

Falke, M.

Subtelomeric findings in children with autistic behaviour: three case reports

Fastnacht, E.

Can 18FDG-PET detect malignant transformation of neurofibromas in patients with neurofibromatosis type I?

Fauser, S.

Factors influencing surgical outcome in patients with focal cortical dysplasia

Effects of signal-to-noise ratio and averaging in non-invasive source localization of interictal EEG spikes

Phenotype-genotype analyses in patients with focal cortical dysplasias

Feldmann, E.

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Feneberg, R.

Combined EEG and MEG analysis of early tactile evoked activity in patients with focal epilepsies

Ferrarini, A.

Microduplication 22Q11.2 in a child with autistic disorder: clinical and genetic study

Feucht, M.

Epilepsy surgery in children with tuberous sclerosis

Fiedler, B.

Herpes Simplex Encephalitis: Progressive MRI-deterioration despite clinical stabilization with Acyclovir

Dissociative disorders – from a neuropediatric point of view

Fiedler, B. J.

Cognitive outcome of postpubertal patients with benign partial epilepsy with centrotemporal sharp waves (type Rolando) in childhood and adolescence

Figura, K. von

Clinical and molecular characterization of patients with multiple sulfatase deficiency

Filz, C.

Elective mutism, generalized seizures, developmental delay, mild mental retardation, dysmorphic features and renal dystopia in a 13-year-old boy – a case report

Fink, G.

Neurophysiological correlates of relatively enhanced local visual search in healthy and autistic adolescents

Fink, H.

Neurodegeneration in newborn rats following general anesthesia

Finsterbusch, J.

Leukoencephalopathy with brain stem and spinal cord involvement and elevated white matter lactate (LBSL): Serial proton MRS and DTI of a child over a period of 6 years

Flentje, M.

High rates of early relapses after complete resection and early tumor progressions after incomplete resection of childhood craniopharyngioma – update after three years of prospective evaluation in KRANIOPHARYNGEOM 2000

First randomized multicenter study in patients with childhood craniopharyngioma analyzing the appropriate time point of irradiation after incomplete resection – study design of KRANIOPHARYNGEOM 2007

Foerster, S.

Therapy with ACTH versus pulsatile corticoid – retrospective analysis of efficacy in treatment of infantile epilepsy syndromes

Clinical experience using a rapid loading dose of levetiracetam in childhood epilepsy

Frahm, J.

Leukoencephalopathy with brain stem and spinal cord involvement and elevated white matter lactate (LBSL): Serial proton MRS and DTI of a child over a period of 6 years

Franz, A. R.

Late diagnosis of pyridoxal- phosphate depending epilepsy: Case report of a 5 year old boy

Freisinger, P.

Tuberous sclerosis and cystic kidney disease

Friebel, D.

Fulminant course of subacute sclerosing panencephalitis in an infant: electroencephalography as a guiding diagnostic instrument

Friedrich, M.

Thickening of the dura mater T3-T9– incidental finding or manifestation of neuroborreliosis?

Frings, L.

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Fuchs, S.

Ptosis, microcephaly and delayed motor development as main clinical manifestations in a female patient with chromosome 18p deletion-syndrome

Fues, A.

Does valproic acid cause cardiac arrhythmias, in particular QT-prolongations, as possible SUDEP risk factor?

Gal, A.

Economical diagnosis of neuronal ceroid lipofuscinoses

Ptosis, microcephaly and delayed motor development as main clinical manifestations in a female patient with chromosome 18p deletion-syndrome

Gandolfo, C.

Sinus Pericranii: Diagnostic and therapeutic considerations

Garkisch, S.

KCNQ3 and KCNQ2 mutations contribute to rare and common forms of idiopathic epilepsy

Gärtner, J.

Treatment of epilepsy in patients with Rett syndrome

Leukoencephalopathy with brain stem and spinal cord involvement and elevated white matter lactate (LBSL): Serial proton MRS and DTI of a child over a period of 6 years

Rational diagnostic for Zellweger Syndrome and other peroxisomal biogenesis defects

Frequency, Genotypic and Phenotypic Spectrum of Pelizaeus Merzbacher-like Disease caused by GJA12 Mutations

Clinical and molecular characterization of patients with multiple sulfatase deficiency

Gebhardt, U.

High rates of early relapses after complete resection and early tumor progressions after incomplete resection of childhood craniopharyngioma – update after three years of prospective evaluation in KRANIOPHARYNGEOM 2000

History and symptoms at primary diagnosis of childhood craniopharyngioma in 311 patients

Melatonin treatment in obese patients with childhood craniopharyngioma and increased daytime sleepiness

Quality of life (QoL) in childhood craniopharyngioma – current status of the prospective multicenter study KRANIOPHARYNGEOM 2000 and results of a retrospective study on 185 long-term survivors

Reduced sympathetic metabolites in urine of obese patients with craniopharyngioma

Secondary narcolepsy may be a causative factor of increased daytime sleepiness in obese patients with childhood craniopharyngioma

First randomized multicenter study in patients with childhood craniopharyngioma analyzing the appropriate time point of irradiation after incomplete resection – study design of KRANIOPHARYNGEOM 2007

Geis, T.

Treatment failure in idiopathic intracranial hypertension in a male teenager

Gempel, K.

3-methylglutaconic aciduria in mitochondrial encepahlopathy: 2 case reports

Gensthaler, A.

Elective mutism, generalized seizures, developmental delay, mild mental retardation, dysmorphic features and renal dystopia in a 13-year-old boy – a case report

Gerhard, U. J.

The 22q11 deletion syndrome poses a multidisciplinary challenge for pediatricians and child psychiatrists as shown by a case report

Gerlach, R.

Bilateral decompressive craniectomy in a predominantly hypoxic brain damage

Gerstl, E. M.

Tuberous sclerosis and cystic kidney disease

Gerstl, J.

Thickening of the dura mater T3-T9– incidental finding or manifestation of neuroborreliosis?

Gerstl, L.

Papillary hypothalamic tumour in a patient with tuberous sclerosis: A case report

Gerstner, T.

Valproic Acid associated encephalopathy –19 new cases in Germany from 1994 to 2003– a side effect associated to VPA-therapy not only in young children

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Gerwe, M.

Transition from immediate-release methylphenidate (IR-MPH) to extended-release methylphenidate (Oros®-MPH, Concerta®) is associated with an improvement in quality of life in patients with ADHD – results from an open label naturalistic study

Gil, P.

Ubiquitin-Proteasome pathway alteration in distal myopathy due to a mutation in a novel kelch protein

Gläser, A.

Ophthalmological examination after a first seizure in paediatric patients are of low diagnostic value

Gloger, C.

Dystonia or hysteria? A case study in respect of the neuropsychiatric problems after implantation

Golla, G.

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Greiner, P.

Relevance of abdominal fluid for the assessment of ventriculoperitoneal shunt function in children

Gressens, P.

Pharmacological inhibition of NADPH oxidase does not reduce excitotoxic brain lesion in newborn mice

Granulocyte-Colony stimulating factor reduces brain injury in newborn mice when given after the acute phase of brain injury

Dextromethorphan an „old“ drug to protect the newborn brain against perinatal injury?

Griesmaier, E.

Pharmacological inhibition of NADPH oxidase does not reduce excitotoxic brain lesion in newborn mice

Granulocyte-Colony stimulating factor reduces brain injury in newborn mice when given after the acute phase of brain injury

Dextromethorphan an „old“ drug to protect the newborn brain against perinatal injury?

Grodd, W.

Cerebellar activation in right-hemispheric language dominance following early left-sided brain lesions

Gross, C.

Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K)

Groß, D.

Effect of early intervention on infantile postural asymmetry: a prospective 2 years follow-up

Gruber, R.

No correlation for MDR1 polymorphisms and pharmacoresistent epilepsy in children

Gumbinger, C.

Phenotype-genotype analyses in patients with focal cortical dysplasias

Haas, J. P.

Loss of vertical gaze – the Parinaud syndrome

Haberlandt, E.

Effect of valproic acid treatment on body composition, leptin and soluble leptin receptor in epileptic children

Therapy with ACTH versus pulsatile corticoid – retrospective analysis of efficacy in treatment of infantile epilepsy syndromes

Clinical experience using a rapid loading dose of levetiracetam in childhood epilepsy

3-Heptanone in exhaled breath gas of patients with propionic acidemia and therapy with valproate

Urea cycle defects: Changes of amino acid CSF/plasma-ratios

Hadyk, T.

Intracortical inhibition in patients suffering from congenital hemiparesis

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a TMS study

Häffner, M.

Phenotype-genotype analyses in patients with focal cortical dysplasias

Hagen, M. von der

Magnetic resonance imaging of skeletal muscles reveals a distinct pattern of muscle involvement in a family with congenital myopathy caused by a RYR1 mutation

Aicardi-Goutières syndrome: clinical, laborchemical and neuroradiological findings in the first two years of life of an early diagnosed patient

Fulminant course of subacute sclerosing panencephalitis in an infant: electroencephalography as a guiding diagnostic instrument

Muscle Magnetic-Resonance-Imaging as diagnostic tool in patients with autosomal- recessive limb girdle muscular dystrophy (LGMD2)

Hahn, A.

KCNQ3 and KCNQ2 mutations contribute to rare and common forms of idiopathic epilepsy

Inspiratory muscle load during stenotic breathing in children with neuromuscular diseases

MRI- and neurophysiological findings in a case of Horizontal Gaze Palsy with Progressive Scoliosis (HGPPS)

Assessment of the respiratory center output in children with neuromuscular diseases

Hahn, G.

Magnetic resonance imaging of skeletal muscles reveals a distinct pattern of muscle involvement in a family with congenital myopathy caused by a RYR1 mutation

Aicardi-Goutières syndrome: clinical, laborchemical and neuroradiological findings in the first two years of life of an early diagnosed patient

Fulminant course of subacute sclerosing panencephalitis in an infant: electroencephalography as a guiding diagnostic instrument

Muscle Magnetic-Resonance-Imaging as diagnostic tool in patients with autosomal- recessive limb girdle muscular dystrophy (LGMD2)

Hahn, H.

Tuberous sclerosis and cystic kidney disease

Haller, S.

Horizontal gaze palsy with progressive scoliosis

Hambrecht, S.

Febrile seizures, loss of consciousness, EEG-patterns with focal and diffuse slowing, epilepsy in the family history – no epilepsy?

Hamm, A.

Neurophysiological correlatives of eating behavior in obese children and adolescents

Handwerker, G.

Melatonin treatment in obese patients with childhood craniopharyngioma and increased daytime sleepiness

Secondary narcolepsy may be a causative factor of increased daytime sleepiness in obese patients with childhood craniopharyngioma

Psychiatric disorders in pediatric outpatient care

Hanke, K.

Vagus nerve stimulation and heart rate – the influence of vagus nerve stimulation output current on heart rate

Hansen, H. H.

Cannabinoids enhance the susceptibility of the immature brain to ethanol neurotoxicity

Harding, P.

Therapy resistant epilepsia partialis continua as leading symptom of Alpers disease

Hargarter, L.

Transition from immediate-release methylphenidate (IR-MPH) to extended-release methylphenidate (Oros®-MPH, Concerta®) is associated with an improvement in quality of life in patients with ADHD – results from an open label naturalistic study

Harting, I.

Combined EEG and MEG analysis of early tactile evoked activity in patients with focal epilepsies

Effects of signal-to-noise ratio and averaging in non-invasive source localization of interictal EEG spikes

Hartmann, M.

Psychopathology of Batten Disease (BD)

Hasilik, M.

Partial trisomy 5p and deletion of the 1p region causes severe psychomotor delay, refractory epilepsy and cleft lip and palate in a 10-year old girl – a long way to diagnosis

Ptosis, microcephaly and delayed motor development as main clinical manifestations in a female patient with chromosome 18p deletion-syndrome

Hattersley, A.

Symptomatic west syndrome in neonatal diabetes and developmental delay (DEND-syndrome)?

Hauch, H.

Thickening of the dura mater T3-T9– incidental finding or manifestation of neuroborreliosis?

Häusler, M.

Subaponeurotic fluid-collection after birth- a self limiting cerebrospinal fluid fistula?

Successful continuous lumbar intrathecal interferon alpha treatment in SSPE

Neurological manifestations of EBV infection: a heterogeneous disease entity

Atypical presentations of herpes simplex virus encephalitis

Heckel, M.

Successfull therapy with Rituximab in an adolescent patient with severe multiple sclerosis

Heep, A.

Hemimegalencephaly – long-term follow up after functional hemispherectomy

Cerebrospinal fluid obstruction and CSF malresorption: Analysis of specific CSF biomarkers indicative for growth factor- and fibrosis- related CSF malabsorption in neonatal hydrocephalus

Hehr, U.

Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K)

Heinen, F.

Sodium channel influencing drugs may provoke refractory status epilepticus in patients with SCN1A-mutations!

Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option?

Formation of antibodies against botulinum toxin B after treatment of drooling in two children with cerebral palsy

Feasibility and first results of a binational, bicenter trial of locomotor therapy with a driven gait orthosis in children with central gait impairment

Heinrich, U.

Interstitial deletion (2)(q11.2-q21) in a newborn with multiple malformations

Subtelomeric findings in children with autistic behaviour: three case reports

Heinz-Erian, P.

Urea cycle defects: Changes of amino acid CSF/plasma-ratios

Helms, G.

Leukoencephalopathy with brain stem and spinal cord involvement and elevated white matter lactate (LBSL): Serial proton MRS and DTI of a child over a period of 6 years

Henneke, M.

Frequency, Genotypic and Phenotypic Spectrum of Pelizaeus Merzbacher-like Disease caused by GJA12 Mutations

Henschel, V.

Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option?

Herbertz, S.

Ophthalmological examination after a first seizure in paediatric patients are of low diagnostic value

Does barefoot walking alter the manifestation of idiopathic toe walking? – Low prevalence among the children slum population of Dhaka (Bangladesh)

Value and cost-benefit analysis of in-patient diagnosis of developmental retardation

Herm, M.

GTPCH enzyme activity in patients with suspected dopa-responsive dystonia

Hermann, E.

Bilateral decompressive craniectomy in a predominantly hypoxic brain damage

Herpertz-Dahlmann, B.

Neurophysiological correlates of relatively enhanced local visual search in healthy and autistic adolescents

Herrmann, R.

Ubiquitin-Proteasome pathway alteration in distal myopathy due to a mutation in a novel kelch protein

Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K)

Herting, E.

Tuberous Sclerosis Complex as a cause of prenatally diagnosed polycystic kidney disease

Hertzberg, C.

Partial trisomy 5p and deletion of the 1p region causes severe psychomotor delay, refractory epilepsy and cleft lip and palate in a 10-year old girl – a long way to diagnosis

Hetzel, P.

Mismatch detection: an auditory event-related study to detect differences in pre-attentive and learning capability of fullterm and preterm newborns

Heuvel, B. van den

Therapy resistant epilepsia partialis continua as leading symptom of Alpers disease

Hillenbrand, B.

Febrile seizures, loss of consciousness, EEG-patterns with focal and diffuse slowing, epilepsy in the family history – no epilepsy?

Zonisamide in refractory epilepsies of childood and adolescence

Hinderlich, S.

Ubiquitin-Proteasome pathway alteration in distal myopathy due to a mutation in a novel kelch protein

Hirschfeld, H.

Neurophysiological correlatives of eating behavior in obese children and adolescents

Hoechstetter, K.

Combined EEG and MEG analysis of early tactile evoked activity in patients with focal epilepsies

Effects of signal-to-noise ratio and averaging in non-invasive source localization of interictal EEG spikes

Hoffmann, G. F.

Late diagnosis of pyridoxal- phosphate depending epilepsy: Case report of a 5 year old boy

GTPCH enzyme activity in patients with suspected dopa-responsive dystonia

Hoffmann, K.

Ubiquitin-Proteasome pathway alteration in distal myopathy due to a mutation in a novel kelch protein

Hofmann-Peters, A.

ZONISAMIDE – Clinical experiences in 20 pharmacoresistant children and adolescents

Höger, P.

Gingival hyperplasia in children treated with valproate: A case report

Holland, K. D.

To evaluate the effectiveness of topiramate (TPM) monotherapy or add-on therapy in patients with juvenile myoclonic epilepsy (JME)

Holthausen, H.

No correlation for MDR1 polymorphisms and pharmacoresistent epilepsy in children

Menkes-Syndrome: Delayed diagnosis because of misinterpretation as battered child syndrome in 2 of 3 children in 2006

Long term use of zonisamide in refractory childhood-onset epilepsy

Sodium channel influencing drugs may provoke refractory status epilepticus in patients with SCN1A-mutations!

Hörster, F.

GTPCH enzyme activity in patients with suspected dopa-responsive dystonia

Horvath, J.

Ependymal cilia exhibit a cell-type specific axonemal distribution of outer dynein arm proteins

Hoving, E.

Cerebrospinal fluid obstruction and CSF malresorption: Analysis of specific CSF biomarkers indicative for growth factor- and fibrosis- related CSF malabsorption in neonatal hydrocephalus

Howell, T.

Loss of vertical gaze – the Parinaud syndrome

Hübner, C.

A new form of spinal muscular atrophy

Huebner, A.

Magnetic resonance imaging of skeletal muscles reveals a distinct pattern of muscle involvement in a family with congenital myopathy caused by a RYR1 mutation

Huisman, T. A.

Pontine involvement as an imaging feature of severe hypoxic-ischemic encephalopathy in the term neonate

Failure of decussation of important pathways demonstrated by MR tractography in Joubert syndrome

Hulihan, J.

Randomized dose-controlled multicenter study of topiramate as first line therapy in adolescents with epilepsy

Humpel, C.

Pharmacological inhibition of NADPH oxidase does not reduce excitotoxic brain lesion in newborn mice

Hunneman, D. H.

Reduced sympathetic metabolites in urine of obese patients with craniopharyngioma

Elevated urine catecholamine metabolites: Indicating parameters for identification of Costello syndrome

Huppke, P.

Treatment of epilepsy in patients with Rett syndrome

Leukoencephalopathy with brain stem and spinal cord involvement and elevated white matter lactate (LBSL): Serial proton MRS and DTI of a child over a period of 6 years

Hußmann, O.

MRI- and neurophysiological findings in a case of Horizontal Gaze Palsy with Progressive Scoliosis (HGPPS)

Ikonomidou, C.

Cannabinoids enhance the susceptibility of the immature brain to ethanol neurotoxicity

Neurodegeneration in newborn rats following general anesthesia

Decreased midbrain grey matter after prenatal exposure to antiepileptic drugs

Ikonomidou, H.

Aicardi-Goutières syndrome: clinical, laborchemical and neuroradiological findings in the first two years of life of an early diagnosed patient

Fulminant course of subacute sclerosing panencephalitis in an infant: electroencephalography as a guiding diagnostic instrument

Jagdhuhn, M.

Neurophysiological correlatives of eating behavior in obese children and adolescents

Janauschek, M.

Rare causes of hemicrania in childhood and youth

Janzarik, W. G.

Detection of a KRAS Mutation in a Pilocytic Astrocytoma

Jenke, A.

Absence epilepsy and BECTS: just accident or genetics?

Johannsen, J.

Partial trisomy 5p and deletion of the 1p region causes severe psychomotor delay, refractory epilepsy and cleft lip and palate in a 10-year old girl – a long way to diagnosis

Ptosis, microcephaly and delayed motor development as main clinical manifestations in a female patient with chromosome 18p deletion-syndrome

Juengling, F.

Decreased midbrain grey matter after prenatal exposure to antiepileptic drugs

Jung, T.

Effect of early intervention on infantile postural asymmetry: a prospective 2 years follow-up

Jünger, C. H.

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

Jünger, H.

Reorganization in congenital hemiparesis: fMRI activation of ipsilateral basal ganglia during paretic hand movement

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a fMRI study

Kafadar, I.

Inspiratory muscle load during stenotic breathing in children with neuromuscular diseases

Assessment of the respiratory center output in children with neuromuscular diseases

Kaindl, A. M.

Magnetic resonance imaging of skeletal muscles reveals a distinct pattern of muscle involvement in a family with congenital myopathy caused by a RYR1 mutation

Kaiser, J.

Frequency, Genotypic and Phenotypic Spectrum of Pelizaeus Merzbacher-like Disease caused by GJA12 Mutations

Kapeller, E.

Pharmacological inhibition of NADPH oxidase does not reduce excitotoxic brain lesion in newborn mice

Karall, D.

Effect of valproic acid treatment on body composition, leptin and soluble leptin receptor in epileptic children

Therapy with ACTH versus pulsatile corticoid – retrospective analysis of efficacy in treatment of infantile epilepsy syndromes

3-Heptanone in exhaled breath gas of patients with propionic acidemia and therapy with valproate

Urea cycle defects: Changes of amino acid CSF/plasma-ratios

Karenfort, M.

Successfull therapy with Rituximab in an adolescent patient with severe multiple sclerosis

Kaskel-Paul, S.

Progressive hearing loss as presenting symptom of benign intracranial hypertension

Kassubek, J.

Decreased midbrain grey matter after prenatal exposure to antiepileptic drugs

Kehrer, C.

Early symptoms and time period from the occurrence of first symptoms to the diagnosis of metachromatic leucodystrophy (MLD)

Keimer, R.

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Efficacy of interstitial radiosurgery in the treatment of pharmacoresistant gelastic epilepsy due to hypothalamic hamartomas

Keller, M.

Pharmacological inhibition of NADPH oxidase does not reduce excitotoxic brain lesion in newborn mice

Granulocyte-Colony stimulating factor reduces brain injury in newborn mice when given after the acute phase of brain injury

Dextromethorphan an „old“ drug to protect the newborn brain against perinatal injury?

Kentrup, H.

Atypical presentations of herpes simplex virus encephalitis

Keppler, J.

Fatal course of a mycoplasma hominis- and ureaplasma urealyticum-meningitis in a very low birth weight infant

Kerner, T.

Neurodegeneration in newborn rats following general anesthesia

Kiefer, C.

Reactivation of bilateral cognitive networks after stroke in childhood

Kiefer, P.

Subaponeurotic fluid-collection after birth- a self limiting cerebrospinal fluid fistula?

Kieslich, M.

Cognitive long- term outcomes after acute lymphoblastic leukaemia in childhood

Does valproic acid cause cardiac arrhythmias, in particular QT-prolongations, as possible SUDEP risk factor?

Bilateral decompressive craniectomy in a predominantly hypoxic brain damage

Retrobulbar pain, diplopia and exophthalmus as manifestations of an isolated ocular myositis in a 15 year old boy

Posterior Reversible Encephalopathy Syndrome (PRES) in children – a single-institution retrosprective study

Primary pseudotumor cerebri in association with obesity – a rare differential diagnosis even in childhood

Kleber, M.

Gait disturbance as a first sign of SSPE in early infancy

Klein, C.

Detection of a KRAS Mutation in a Pilocytic Astrocytoma

DYT11– Myoclonic Dystonia as a rare form of childhood dystonia

Kleines, M.

Successful continuous lumbar intrathecal interferon alpha treatment in SSPE

Neurological manifestations of EBV infection: a heterogeneous disease entity

Atypical presentations of herpes simplex virus encephalitis

Klepper, J.

Late diagnosis of pyridoxal- phosphate depending epilepsy: Case report of a 5 year old boy

Kluger, G.

No correlation for MDR1 polymorphisms and pharmacoresistent epilepsy in children

Neuropediatric aspects in the diagnosis of mentally retarded children with autism

Menkes-Syndrome: Delayed diagnosis because of misinterpretation as battered child syndrome in 2 of 3 children in 2006

Long term use of zonisamide in refractory childhood-onset epilepsy

Video and EEG documentation of seizures induced by showering in 2 photosensitive patients

Multiprofessional assessment and treatment of children with autistic disorders

Kluger, G. J.

Sodium channel influencing drugs may provoke refractory status epilepticus in patients with SCN1A-mutations!

Knecht, B.

Feasibility and first results of a binational, bicenter trial of locomotor therapy with a driven gait orthosis in children with central gait impairment

Knobloch, T.

Endoscopic cystoventriculostomy and ventriculocysternostomy using a recently developed 2.0 micron near infrared laser in patients with hydrocephalus

Koch, S.

Decreased midbrain grey matter after prenatal exposure to antiepileptic drugs

Koch-Graus, A.

Developmental testing in early infancy: aspects of stability and change in German preterm born infants and other biological high risk infants

Köhler, K.

Treatment of epilepsy in patients with Rett syndrome

Kohlschütter, A.

Economical diagnosis of neuronal ceroid lipofuscinoses

The NCL-Net: How a network can improve care for patients with rare neurological diseases

Psychopathology of Batten Disease (BD)

Kolb, R.

Quality of life (QoL) in childhood craniopharyngioma – current status of the prospective multicenter study KRANIOPHARYNGEOM 2000 and results of a retrospective study on 185 long-term survivors

König, S.

Valproic Acid associated encephalopathy –19 new cases in Germany from 1994 to 2003– a side effect associated to VPA-therapy not only in young children

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Konrad, K.

Neurophysiological correlates of relatively enhanced local visual search in healthy and autistic adolescents

Korall, H.

Extended selective screening for epilepsies by gas chromatography/mass spectrometry (GC/MS) and tandem mass spectrometry (TMS)

Korenke, G. C.

Elevated urine catecholamine metabolites: Indicating parameters for identification of Costello syndrome

Rare causes of hemicrania in childhood and youth

Therapy resistant epilepsia partialis continua as leading symptom of Alpers disease

Korinth, M.

Subaponeurotic fluid-collection after birth- a self limiting cerebrospinal fluid fistula?

Korinthenberg, R.

Detection of a KRAS Mutation in a Pilocytic Astrocytoma

Phenotype-genotype analyses in patients with focal cortical dysplasias

Relevance of abdominal fluid for the assessment of ventriculoperitoneal shunt function in children

Validity and responsiveness of the GMFM-66 for children and adolescents with traumatic brain injury

Kornbrust, A.

Hemimegalencephaly – long-term follow up after functional hemispherectomy

Korn-Merker, E.

ZONISAMIDE – Clinical experiences in 20 pharmacoresistant children and adolescents

Kortmann, R. D.

First randomized multicenter study in patients with childhood craniopharyngioma analyzing the appropriate time point of irradiation after incomplete resection – study design of KRANIOPHARYNGEOM 2007

Köster, B.

Progressive hearing loss as presenting symptom of benign intracranial hypertension

Kostoviæ, I.

The structural basis of developmental plasticity in the human brain

Kountouris, D.

Alexithymia in children, is it a brain disorder?

Krägeloh-Mann, I.

Cerebellar activation in right-hemispheric language dominance following early left-sided brain lesions

Developmental outcome of children conceived by ICSI at 5 years of age

Early symptoms and time period from the occurrence of first symptoms to the diagnosis of metachromatic leucodystrophy (MLD)

17-year-old boy with atypical mild clinical course of Canavan disease

Kratz, C.

Detection of a KRAS Mutation in a Pilocytic Astrocytoma

Krause, C.

Rational diagnostic for Zellweger Syndrome and other peroxisomal biogenesis defects

Krauss, J.

Papillary hypothalamic tumour in a patient with tuberous sclerosis: A case report

Krauß, J.

The role of endoscopic procedures in hydrocephalus therapy

Kremer, P.

Trigeminal neuralgia in children – differential therapy and neurosurgical indication

Kress, W.

Magnetic resonance imaging of skeletal muscles reveals a distinct pattern of muscle involvement in a family with congenital myopathy caused by a RYR1 mutation

Krings, T.

Sinus Pericranii: Diagnostic and therapeutic considerations

Kruse, B.

Symptomatic west syndrome in neonatal diabetes and developmental delay (DEND-syndrome)?

Partial trisomy 5p and deletion of the 1p region causes severe psychomotor delay, refractory epilepsy and cleft lip and palate in a 10-year old girl – a long way to diagnosis

Ptosis, microcephaly and delayed motor development as main clinical manifestations in a female patient with chromosome 18p deletion-syndrome

Krutz, B.

Cannabinoids enhance the susceptibility of the immature brain to ethanol neurotoxicity

Kuhnke, N.

An optimized scheme of motor learning

Intracortical inhibition in patients suffering from congenital hemiparesis

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a TMS study

Kurlemann, G.

KCNQ3 and KCNQ2 mutations contribute to rare and common forms of idiopathic epilepsy

Herpes Simplex Encephalitis: Progressive MRI-deterioration despite clinical stabilization with Acyclovir

Dissociative disorders – from a neuropediatric point of view

Cognitive outcome of postpubertal patients with benign partial epilepsy with centrotemporal sharp waves (type Rolando) in childhood and adolescence

Kustermann-Kuhn, B.

Early symptoms and time period from the occurrence of first symptoms to the diagnosis of metachromatic leucodystrophy (MLD)

Kutsche, K.

Elevated urine catecholamine metabolites: Indicating parameters for identification of Costello syndrome

Kutschke, G.

Sensory motor neuropathy, myopathy, white matter abnormalities and lethal intestinal motility disturbance in a 15 years old boy – mitochondrial dysfunction due to thymidine phosphoryase deficiency

Laage-Gaupp, A.

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

Laimer, M.

Effect of valproic acid treatment on body composition, leptin and soluble leptin receptor in epileptic children

Lämmer, C.

Follow-up of tuberous sclerosis in 3 year-old boy – a case report

Lampe, C.

Sensory motor neuropathy, myopathy, white matter abnormalities and lethal intestinal motility disturbance in a 15 years old boy – mitochondrial dysfunction due to thymidine phosphoryase deficiency

Landes, V.

Intracortical inhibition in patients suffering from congenital hemiparesis

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a TMS study

Larisch, R.

Can 18FDG-PET detect malignant transformation of neurofibromas in patients with neurofibromatosis type I?

Lasjaunias, P.

Sinus Pericranii: Diagnostic and therapeutic considerations

Lauffer, H.

Neurophysiological correlatives of eating behavior in obese children and adolescents

Lebrun, A. H.

Economical diagnosis of neuronal ceroid lipofuscinoses

Lee, S. H.

Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option?

Lee-Kirsch, M.

Aicardi-Goutières syndrome: clinical, laborchemical and neuroradiological findings in the first two years of life of an early diagnosed patient

Legius, E.

Can 18FDG-PET detect malignant transformation of neurofibromas in patients with neurofibromatosis type I?

Lehmkuhl, U.

Decreased midbrain grey matter after prenatal exposure to antiepileptic drugs

Lehrnbecher, T.

Posterior Reversible Encephalopathy Syndrome (PRES) in children – a single-institution retrosprective study

Leiz, S.

Clinical and behavioural phenotype in a contiguous gene deletion syndrome at Xp22.3

Lenz, A.

Follow-up of tuberous sclerosis in 3 year-old boy – a case report

Levisohn, P.

To evaluate the effectiveness of topiramate (TPM) monotherapy or add-on therapy in patients with juvenile myoclonic epilepsy (JME)

Licht, P.

Developmental outcome of children conceived by ICSI at 5 years of age

Lidzba, K.

Cerebellar activation in right-hemispheric language dominance following early left-sided brain lesions

Reactivation of bilateral cognitive networks after stroke in childhood

Developmental outcome of children conceived by ICSI at 5 years of age

Ligges, M.

Elective mutism, generalized seizures, developmental delay, mild mental retardation, dysmorphic features and renal dystopia in a 13-year-old boy – a case report

Linder-Lucht, M.

Reorganization in congenital hemiparesis: fMRI activation of ipsilateral basal ganglia during paretic hand movement

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a fMRI study

Integrity of the corticospinal system in children with bilateral cerebral palsy and periventricular leukomalacia: A transcranial magnetic stimulation study

Validity and responsiveness of the GMFM-66 for children and adolescents with traumatic brain injury

Lindner, T.

Ubiquitin-Proteasome pathway alteration in distal myopathy due to a mutation in a novel kelch protein

Lischetzki, G.

A cerebral sinus thrombosis in a 4 year old child

Lochmüller, H.

A new form of spinal muscular atrophy

Loges, N.

Ependymal cilia exhibit a cell-type specific axonemal distribution of outer dynein arm proteins

Loges, N. T.

Detection of a KRAS Mutation in a Pilocytic Astrocytoma

Lommel, M.

Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K)

Longin, E.

Valproic Acid associated encephalopathy –19 new cases in Germany from 1994 to 2003– a side effect associated to VPA-therapy not only in young children

Lorenz, I.

A cerebral sinus thrombosis in a 4 year old child

Ludwig, H. C.

Endoscopic cystoventriculostomy and ventriculocysternostomy using a recently developed 2.0 micron near infrared laser in patients with hydrocephalus

Luef, G.

Effect of valproic acid treatment on body composition, leptin and soluble leptin receptor in epileptic children

Lukacs, Z.

Economical diagnosis of neuronal ceroid lipofuscinoses

Luthe, L.

Rare causes of hemicrania in childhood and youth

Lütschg, J.

Mismatch detection: an auditory event-related study to detect differences in pre-attentive and learning capability of fullterm and preterm newborns

Horizontal gaze palsy with progressive scoliosis

Lutz, B.

Cannabinoids enhance the susceptibility of the immature brain to ethanol neurotoxicity

Mall, V.

An optimized scheme of motor learning

Reorganization in congenital hemiparesis: fMRI activation of ipsilateral basal ganglia during paretic hand movement

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a fMRI study

Intracortical inhibition in patients suffering from congenital hemiparesis

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

Integrity of the corticospinal system in children with bilateral cerebral palsy and periventricular leukomalacia: A transcranial magnetic stimulation study

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a TMS study

Validity and responsiveness of the GMFM-66 for children and adolescents with traumatic brain injury

Manjaly, Z.

Neurophysiological correlates of relatively enhanced local visual search in healthy and autistic adolescents

Mansmann, U.

Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option?

Marquardt, I.

Elevated urine catecholamine metabolites: Indicating parameters for identification of Costello syndrome

Therapy resistant epilepsia partialis continua as leading symptom of Alpers disease

Marsicano, G.

Cannabinoids enhance the susceptibility of the immature brain to ethanol neurotoxicity

Mattejat, F.

Transition from immediate-release methylphenidate (IR-MPH) to extended-release methylphenidate (Oros®-MPH, Concerta®) is associated with an improvement in quality of life in patients with ADHD – results from an open label naturalistic study

Mau-Holzmann, U.

Developmental outcome of children conceived by ICSI at 5 years of age

Mayatepek, E.

Seasonal clustering of prepubertal idiopathic intracranial hypertension

Successfull therapy with Rituximab in an adolescent patient with severe multiple sclerosis

Mayer, H.

IQ-decrease by antiepileptic therapy

Meindl, A.

Clinical and behavioural phenotype in a contiguous gene deletion syndrome at Xp22.3

Mennicke, K.

Partial trisomy 5p and deletion of the 1p region causes severe psychomotor delay, refractory epilepsy and cleft lip and palate in a 10-year old girl – a long way to diagnosis

Menzel, U.

Symptomatic west syndrome in neonatal diabetes and developmental delay (DEND-syndrome)?

Merkenschlager, A.

Ophthalmological examination after a first seizure in paediatric patients are of low diagnostic value

Does barefoot walking alter the manifestation of idiopathic toe walking? – Low prevalence among the children slum population of Dhaka (Bangladesh)

Value and cost-benefit analysis of in-patient diagnosis of developmental retardation

Merz, U.

Atypical presentations of herpes simplex virus encephalitis

Messing-Juenger, M.

Can 18FDG-PET detect malignant transformation of neurofibromas in patients with neurofibromatosis type I?

Meyer-Heim, A.

Feasibility and first results of a binational, bicenter trial of locomotor therapy with a driven gait orthosis in children with central gait impairment

Michaelis, I.

17-year-old boy with atypical mild clinical course of Canavan disease

Michaelis, U.

Validity and responsiveness of the GMFM-66 for children and adolescents with traumatic brain injury

Michaelis, U. S.

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

Morath, M. A.

Severe secondary mitochondrial dysfunction in classical organic acidemias

Motz, R.

Elevated urine catecholamine metabolites: Indicating parameters for identification of Costello syndrome

Muhle, H.

DYT11– Myoclonic Dystonia as a rare form of childhood dystonia

Müller, H. L.

High rates of early relapses after complete resection and early tumor progressions after incomplete resection of childhood craniopharyngioma – update after three years of prospective evaluation in KRANIOPHARYNGEOM 2000

History and symptoms at primary diagnosis of childhood craniopharyngioma in 311 patients

Melatonin treatment in obese patients with childhood craniopharyngioma and increased daytime sleepiness

Quality of life (QoL) in childhood craniopharyngioma – current status of the prospective multicenter study KRANIOPHARYNGEOM 2000 and results of a retrospective study on 185 long-term survivors

Reduced sympathetic metabolites in urine of obese patients with craniopharyngioma

Secondary narcolepsy may be a causative factor of increased daytime sleepiness in obese patients with childhood craniopharyngioma

First randomized multicenter study in patients with childhood craniopharyngioma analyzing the appropriate time point of irradiation after incomplete resection – study design of KRANIOPHARYNGEOM 2007

Müller, S.

Rare causes of hemicrania in childhood and youth

Effect of early intervention on infantile postural asymmetry: a prospective 2 years follow-up

Müller, U.

KCNQ3 and KCNQ2 mutations contribute to rare and common forms of idiopathic epilepsy

Müller-Stöver, S.

Secondary narcolepsy may be a causative factor of increased daytime sleepiness in obese patients with childhood craniopharyngioma

Mullik, A.

Does barefoot walking alter the manifestation of idiopathic toe walking? – Low prevalence among the children slum population of Dhaka (Bangladesh)

Neinert, J.

Can 18FDG-PET detect malignant transformation of neurofibromas in patients with neurofibromatosis type I?

Nerlich, A.

Tuberous sclerosis and cystic kidney disease

Neubauer, B.

KCNQ3 and KCNQ2 mutations contribute to rare and common forms of idiopathic epilepsy

Sodium channel influencing drugs may provoke refractory status epilepticus in patients with SCN1A-mutations!

Neubauer, B. A.

Inspiratory muscle load during stenotic breathing in children with neuromuscular diseases

MRI- and neurophysiological findings in a case of Horizontal Gaze Palsy with Progressive Scoliosis (HGPPS)

Assessment of the respiratory center output in children with neuromuscular diseases

Autism and Epilepsy

Neubauer, V.

Granulocyte-Colony stimulating factor reduces brain injury in newborn mice when given after the acute phase of brain injury

Neuberger, J.

Defect of peroxisomal beta oxidation with polymicrogyria, epilepsy and myopathy in a newborn

Neumann, D.

Zonisamide in refractory epilepsies of childood and adolescence

IQ-decrease by antiepileptic therapy

Ney, S.

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

Niemeyer, C.

Detection of a KRAS Mutation in a Pilocytic Astrocytoma

Nies, H.

Progressive hearing loss as presenting symptom of benign intracranial hypertension

Niesytto, C.

Loss of vertical gaze – the Parinaud syndrome

Niggemann, P.

Subaponeurotic fluid-collection after birth- a self limiting cerebrospinal fluid fistula?

Nikolai, T.

Sodium channel influencing drugs may provoke refractory status epilepticus in patients with SCN1A-mutations!

Nögel, S. C.

3-methylglutaconic aciduria in mitochondrial encepahlopathy: 2 case reports

Noterdaeme, M.

Neuropediatric aspects in the diagnosis of mentally retarded children with autism

Neuropediatric problems in child and adolescent psychiatry

Neuropsychological assessment of language and cognition in children with autistic disorders

Multiprofessional assessment and treatment of children with autistic disorders

Early diagnosis of autistic disorders: is a differentiation between autism, language disorder, attention deficit disorder and mental retardation possible?

Nürnberg, G.

A new form of spinal muscular atrophy

Nürnberg, P.

A new form of spinal muscular atrophy

Nüsken, E.

Acute encephalopathy as the presenting symptom in Henoch-Schoenlein purpura: A case report

Oberman, B.

Sensory motor neuropathy, myopathy, white matter abnormalities and lethal intestinal motility disturbance in a 15 years old boy – mitochondrial dysfunction due to thymidine phosphoryase deficiency

Oesch, V.

Diagnostic errors in shunt dysfunction

Ohlenbusch, A.

Frequency, Genotypic and Phenotypic Spectrum of Pelizaeus Merzbacher-like Disease caused by GJA12 Mutations

Olbrich, H.

Detection of a KRAS Mutation in a Pilocytic Astrocytoma

Ependymal cilia exhibit a cell-type specific axonemal distribution of outer dynein arm proteins

Omogbehin, P.

Is less more? Trend of epileptic seizures and behavior in a TSC 1 patient with and without anticonvulsant treatment

Omran, H.

Detection of a KRAS Mutation in a Pilocytic Astrocytoma

Ependymal cilia exhibit a cell-type specific axonemal distribution of outer dynein arm proteins

Opladen, T.

GTPCH enzyme activity in patients with suspected dopa-responsive dystonia

Orth, U.

Economical diagnosis of neuronal ceroid lipofuscinoses

Ostertag, C.

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Efficacy of interstitial radiosurgery in the treatment of pharmacoresistant gelastic epilepsy due to hypothalamic hamartomas

Oswald, S.

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

Othmer, V.

Validity and responsiveness of the GMFM-66 for children and adolescents with traumatic brain injury

Otte, J.

Distal phalanx necrosis after intra-arterial injection of phenobarbital during treatment of subtle generalized convulsive status epilepticus

Pälmke, M.

Cognitive outcome of postpubertal patients with benign partial epilepsy with centrotemporal sharp waves (type Rolando) in childhood and adolescence

Parbel, S.

Posterior Reversible Encephalopathy Syndrome (PRES) in children – a single-institution retrosprective study

Pascal, N.

Atypical presentations of herpes simplex virus encephalitis

Pescia, G.

Microduplication 22Q11.2 in a child with autistic disorder: clinical and genetic study

Peter, N.

Ubiquitin-Proteasome pathway alteration in distal myopathy due to a mutation in a novel kelch protein

Peters, C.

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Peters, H.

The rule of methylphenidate in the treatment of autism

Is less more? Trend of epileptic seizures and behavior in a TSC 1 patient with and without anticonvulsant treatment

Tuberous Sclerosis with deletion on chromosome 9q and TSC-2-like brain dysplasia but TSC 1- like outcome: a case report

Smith-Magenis syndrome: a case report of improved sleep after treatment with atomoxetin and melatonin

Peters, R.

Gingival hyperplasia in children treated with valproate: A case report

Petersen, B.

DYT11– Myoclonic Dystonia as a rare form of childhood dystonia

Pfister, S.

Detection of a KRAS Mutation in a Pilocytic Astrocytoma

Pfisterer, A.

Defect of peroxisomal beta oxidation with polymicrogyria, epilepsy and myopathy in a newborn

Philippi, H.

Effect of early intervention on infantile postural asymmetry: a prospective 2 years follow-up

Pieper, T.

Plasticity of the immature brain- observations from pediatric epilepsy surgery

Pietsch, T.

First randomized multicenter study in patients with childhood craniopharyngioma analyzing the appropriate time point of irradiation after incomplete resection – study design of KRANIOPHARYNGEOM 2007

Pietz, J.

Developmental testing in early infancy: aspects of stability and change in German preterm born infants and other biological high risk infants

Plank, C.

Acute encephalopathy as the presenting symptom in Henoch-Schoenlein purpura: A case report

Plecko, B.

Frequency, Genotypic and Phenotypic Spectrum of Pelizaeus Merzbacher-like Disease caused by GJA12 Mutations

Plischke, H.

No correlation for MDR1 polymorphisms and pharmacoresistent epilepsy in children

Poggenburg, I.

Elevated urine catecholamine metabolites: Indicating parameters for identification of Costello syndrome

Pohl, F.

High rates of early relapses after complete resection and early tumor progressions after incomplete resection of childhood craniopharyngioma – update after three years of prospective evaluation in KRANIOPHARYNGEOM 2000

First randomized multicenter study in patients with childhood craniopharyngioma analyzing the appropriate time point of irradiation after incomplete resection – study design of KRANIOPHARYNGEOM 2007

Polster, T.

Distal phalanx necrosis after intra-arterial injection of phenobarbital during treatment of subtle generalized convulsive status epilepticus

Pomarino, D.

Does barefoot walking alter the manifestation of idiopathic toe walking? – Low prevalence among the children slum population of Dhaka (Bangladesh)

Poretti, A.

Pontine involvement as an imaging feature of severe hypoxic-ischemic encephalopathy in the term neonate

Failure of decussation of important pathways demonstrated by MR tractography in Joubert syndrome

Porto, L.

Cognitive long- term outcomes after acute lymphoblastic leukaemia in childhood

Posterior Reversible Encephalopathy Syndrome (PRES) in children – a single-institution retrosprective study

Pothmann, R.

Trigeminal neuralgia in children – differential therapy and neurosurgical indication

Pragst, F.

Cannabinoids enhance the susceptibility of the immature brain to ethanol neurotoxicity

Preibisch, C.

Cognitive long- term outcomes after acute lymphoblastic leukaemia in childhood

Püst, B.

Gingival hyperplasia in children treated with valproate: A case report

Monosymptomatic rheumatic fever – Chorea Sydenham

Qirshi, M.

Cognitive long- term outcomes after acute lymphoblastic leukaemia in childhood

Bilateral decompressive craniectomy in a predominantly hypoxic brain damage

Retrobulbar pain, diplopia and exophthalmus as manifestations of an isolated ocular myositis in a 15 year old boy

Primary pseudotumor cerebri in association with obesity – a rare differential diagnosis even in childhood

Quiske, A.

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Raabe, C.

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

Ramantani, G.

Levetiracetam in neonatal seizures

Aicardi-Goutières syndrome: clinical, laborchemical and neuroradiological findings in the first two years of life of an early diagnosed patient

Ramelli, G. P.

Clinical manifestations of benign tectal glioma in children and adolescents

Microduplication 22Q11.2 in a child with autistic disorder: clinical and genetic study

Rapp, M.

Tuberous Sclerosis Complex as a cause of prenatally diagnosed polycystic kidney disease

Rating, D.

Combined EEG and MEG analysis of early tactile evoked activity in patients with focal epilepsies

Levetiracetam in neonatal seizures

Effects of signal-to-noise ratio and averaging in non-invasive source localization of interictal EEG spikes

Late diagnosis of pyridoxal- phosphate depending epilepsy: Case report of a 5 year old boy

Rauchenzauner, M.

Effect of valproic acid treatment on body composition, leptin and soluble leptin receptor in epileptic children

Therapy with ACTH versus pulsatile corticoid – retrospective analysis of efficacy in treatment of infantile epilepsy syndromes

Clinical experience using a rapid loading dose of levetiracetam in childhood epilepsy

Urea cycle defects: Changes of amino acid CSF/plasma-ratios

Reifenberger, G.

Can 18FDG-PET detect malignant transformation of neurofibromas in patients with neurofibromatosis type I?

Reiffer, C.

Feasibility and first results of a binational, bicenter trial of locomotor therapy with a driven gait orthosis in children with central gait impairment

Reilich, P.

Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option?

Reinehr, T.

Reduced sympathetic metabolites in urine of obese patients with craniopharyngioma

Reiter, K.

Sodium channel influencing drugs may provoke refractory status epilepticus in patients with SCN1A-mutations!

Reitter, B.

Sensory motor neuropathy, myopathy, white matter abnormalities and lethal intestinal motility disturbance in a 15 years old boy – mitochondrial dysfunction due to thymidine phosphoryase deficiency

Rekate, H. L.

Lessons learned in thirty years of hydocephalus research

Resch, F.

Dissociative Disorders – diagnostic and therapeutic challenges

Reuner, G.

Developmental testing in early infancy: aspects of stability and change in German preterm born infants and other biological high risk infants

Reuner, U.

Muscle Magnetic-Resonance-Imaging as diagnostic tool in patients with autosomal- recessive limb girdle muscular dystrophy (LGMD2)

Richterich, A.

Psychopathology of Batten Disease (BD)

Riebeling, P.

Loss of vertical gaze – the Parinaud syndrome

Ries, M.

Defect of peroxisomal beta oxidation with polymicrogyria, epilepsy and myopathy in a newborn

Riesen, A. van

A new form of spinal muscular atrophy

Rodriguez, D.

Frequency, Genotypic and Phenotypic Spectrum of Pelizaeus Merzbacher-like Disease caused by GJA12 Mutations

Roggendorf, W.

Papillary hypothalamic tumour in a patient with tuberous sclerosis: A case report

Rohayem, J.

Fulminant course of subacute sclerosing panencephalitis in an infant: electroencephalography as a guiding diagnostic instrument

Rohde, V.

Endoscopic cystoventriculostomy and ventriculocysternostomy using a recently developed 2.0 micron near infrared laser in patients with hydrocephalus

Rohsbach, C.

Phenotype-genotype analyses in patients with focal cortical dysplasias

Rosenbaum, T.

Can 18FDG-PET detect malignant transformation of neurofibromas in patients with neurofibromatosis type I?

Progressive hearing loss as presenting symptom of benign intracranial hypertension

Rosewich, H.

Rational diagnostic for Zellweger Syndrome and other peroxisomal biogenesis defects

Rostasy, K.

Endoscopic cystoventriculostomy and ventriculocysternostomy using a recently developed 2.0 micron near infrared laser in patients with hydrocephalus

Roth, C. L.

Reduced sympathetic metabolites in urine of obese patients with craniopharyngioma

Rubens, T.

Defect of peroxisomal beta oxidation with polymicrogyria, epilepsy and myopathy in a newborn

Rüdisser, K.

Tuberous sclerosis and cystic kidney disease

Rupp, A.

Combined EEG and MEG analysis of early tactile evoked activity in patients with focal epilepsies

Effects of signal-to-noise ratio and averaging in non-invasive source localization of interictal EEG spikes

Rutkowski, S.

Papillary hypothalamic tumour in a patient with tuberous sclerosis: A case report

Sanchez Albisua, I.

Developmental outcome of children conceived by ICSI at 5 years of age

Sander, T.

KCNQ3 and KCNQ2 mutations contribute to rare and common forms of idiopathic epilepsy

Sárközy, G.

Granulocyte-Colony stimulating factor reduces brain injury in newborn mice when given after the acute phase of brain injury

Dextromethorphan an „old“ drug to protect the newborn brain against perinatal injury?

Sassen, R.

Hemimegalencephaly – long-term follow up after functional hemispherectomy

Schaaf, M. E.

Sinus Pericranii: Diagnostic and therapeutic considerations

Schaeuble, B.

To evaluate the effectiveness of topiramate (TPM) monotherapy or add-on therapy in patients with juvenile myoclonic epilepsy (JME)

Transition from immediate-release methylphenidate (IR-MPH) to extended-release methylphenidate (Oros®-MPH, Concerta®) is associated with an improvement in quality of life in patients with ADHD – results from an open label naturalistic study

Schäfer, C.

The rule of methylphenidate in the treatment of autism

Schäfer, D. M.

Febrile seizures, loss of consciousness, EEG-patterns with focal and diffuse slowing, epilepsy in the family history – no epilepsy?

Schäfer, J.

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option?

Schäfer, K.

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

Schaller, C.

Cerebrospinal fluid obstruction and CSF malresorption: Analysis of specific CSF biomarkers indicative for growth factor- and fibrosis- related CSF malabsorption in neonatal hydrocephalus

Schallner, J.

Fulminant course of subacute sclerosing panencephalitis in an infant: electroencephalography as a guiding diagnostic instrument

Schäuble, B.

Randomized dose-controlled multicenter study of topiramate as first line therapy in adolescents with epilepsy

Scheer, I.

Decreased midbrain grey matter after prenatal exposure to antiepileptic drugs

Scheithauer, S.

Neurological manifestations of EBV infection: a heterogeneous disease entity

Scherg, M.

Effects of signal-to-noise ratio and averaging in non-invasive source localization of interictal EEG spikes

Scheurlen, W.

Detection of a KRAS Mutation in a Pilocytic Astrocytoma

Schilling, S.

Fatal course of a mycoplasma hominis- and ureaplasma urealyticum-meningitis in a very low birth weight infant

Treatment failure in idiopathic intracranial hypertension in a male teenager

Schlee-Böckh, K.

Is less more? Trend of epileptic seizures and behavior in a TSC 1 patient with and without anticonvulsant treatment

Schlegel, P.

Herpes Simplex Encephalitis: Progressive MRI-deterioration despite clinical stabilization with Acyclovir

Schlotawa, L.

Clinical and molecular characterization of patients with multiple sulfatase deficiency

Schlotter-Weigel, B.

A new form of spinal muscular atrophy

Schmidt, A.

3-Heptanone in exhaled breath gas of patients with propionic acidemia and therapy with valproate

Schmidtlein, C.

Interstitial deletion (2)(q11.2-q21) in a newborn with multiple malformations

First seizure as side effect of an enuresis therapy – a case report

Schmidt-Mader, B.

GTPCH enzyme activity in patients with suspected dopa-responsive dystonia

Schmitt, B.

Pontine involvement as an imaging feature of severe hypoxic-ischemic encephalopathy in the term neonate

Schnellbacher, S.

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Schoberer, A.

Subaponeurotic fluid-collection after birth- a self limiting cerebrospinal fluid fistula?

Scholl-Buergi, S.

Therapy with ACTH versus pulsatile corticoid – retrospective analysis of efficacy in treatment of infantile epilepsy syndromes

Scholl-Bürgi, S.

Effect of valproic acid treatment on body composition, leptin and soluble leptin receptor in epileptic children

3-Heptanone in exhaled breath gas of patients with propionic acidemia and therapy with valproate

Urea cycle defects: Changes of amino acid CSF/plasma-ratios

Schönherr, E.

Effect of valproic acid treatment on body composition, leptin and soluble leptin receptor in epileptic children

Schorle, H.

Hemimegalencephaly – long-term follow up after functional hemispherectomy

Schrader, K.

Symptomatic west syndrome in neonatal diabetes and developmental delay (DEND-syndrome)?

Schramm, J.

Hemimegalencephaly – long-term follow up after functional hemispherectomy

Schröder, C.

Neurophysiological correlatives of eating behavior in obese children and adolescents

Schröder, S.

High rates of early relapses after complete resection and early tumor progressions after incomplete resection of childhood craniopharyngioma – update after three years of prospective evaluation in KRANIOPHARYNGEOM 2000

History and symptoms at primary diagnosis of childhood craniopharyngioma in 311 patients

Quality of life (QoL) in childhood craniopharyngioma – current status of the prospective multicenter study KRANIOPHARYNGEOM 2000 and results of a retrospective study on 185 long-term survivors

Formation of antibodies against botulinum toxin B after treatment of drooling in two children with cerebral palsy

Schroeter, C.

Febrile seizures, loss of consciousness, EEG-patterns with focal and diffuse slowing, epilepsy in the family history – no epilepsy?

Schropp, C.

X-linked hydrocephalus: Another family with a novel mutation in the L1CAM-gene

Papillary hypothalamic tumour in a patient with tuberous sclerosis: A case report

Idiopathic intracranial hypertension – a review over 16 cases in childhood

Schröter, C.

Progressive leftsided cerebellar atrophy and intermittend CSWS-like EEG. Is it Rasmussen Encephalitis?

Zonisamide in refractory epilepsies of childood and adolescence

Schubert, S.

Late diagnosis of pyridoxal- phosphate depending epilepsy: Case report of a 5 year old boy

Schülke, M.

A new form of spinal muscular atrophy

Schulte-Markwort, M.

Psychopathology of Batten Disease (BD)

Schulte-Mönting, J.

Factors influencing surgical outcome in patients with focal cortical dysplasia

Schultz, C.

Tuberous Sclerosis Complex as a cause of prenatally diagnosed polycystic kidney disease

Schulz, A.

Economical diagnosis of neuronal ceroid lipofuscinoses

The NCL-Net: How a network can improve care for patients with rare neurological diseases

Psychopathology of Batten Disease (BD)

Schulze-Bonhage, A.

Factors influencing surgical outcome in patients with focal cortical dysplasia

Effects of signal-to-noise ratio and averaging in non-invasive source localization of interictal EEG spikes

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Efficacy of interstitial radiosurgery in the treatment of pharmacoresistant gelastic epilepsy due to hypothalamic hamartomas

Phenotype-genotype analyses in patients with focal cortical dysplasias

Schumacher, D.

Developmental testing in early infancy: aspects of stability and change in German preterm born infants and other biological high risk infants

Segerer, H.

Fatal course of a mycoplasma hominis- and ureaplasma urealyticum-meningitis in a very low birth weight infant

Treatment failure in idiopathic intracranial hypertension in a male teenager

Seifert, J.

Autism: diagnostic Questions and the clinic Picture

Seiffert, A.

Value and cost-benefit analysis of in-patient diagnosis of developmental retardation

Seiffert, P.

Atypical presentations of herpes simplex virus encephalitis

Sennhauser, F. H.

Feasibility and first results of a binational, bicenter trial of locomotor therapy with a driven gait orthosis in children with central gait impairment

Sifringer, M.

Cannabinoids enhance the susceptibility of the immature brain to ethanol neurotoxicity

Simbruner, G.

Pharmacological inhibition of NADPH oxidase does not reduce excitotoxic brain lesion in newborn mice

Granulocyte-Colony stimulating factor reduces brain injury in newborn mice when given after the acute phase of brain injury

Dextromethorphan an „old“ drug to protect the newborn brain against perinatal injury?

Sival, D.

Cerebrospinal fluid obstruction and CSF malresorption: Analysis of specific CSF biomarkers indicative for growth factor- and fibrosis- related CSF malabsorption in neonatal hydrocephalus

Skopnik, H.

Atypical presentations of herpes simplex virus encephalitis

Smeitink, J. A. M.

Therapy resistant epilepsia partialis continua as leading symptom of Alpers disease

Smitka, M.

Fulminant course of subacute sclerosing panencephalitis in an infant: electroencephalography as a guiding diagnostic instrument

Muscle Magnetic-Resonance-Imaging as diagnostic tool in patients with autosomal- recessive limb girdle muscular dystrophy (LGMD2)

Sörensen, N.

High rates of early relapses after complete resection and early tumor progressions after incomplete resection of childhood craniopharyngioma – update after three years of prospective evaluation in KRANIOPHARYNGEOM 2000

History and symptoms at primary diagnosis of childhood craniopharyngioma in 311 patients

Melatonin treatment in obese patients with childhood craniopharyngioma and increased daytime sleepiness

Quality of life (QoL) in childhood craniopharyngioma – current status of the prospective multicenter study KRANIOPHARYNGEOM 2000 and results of a retrospective study on 185 long-term survivors

Secondary narcolepsy may be a causative factor of increased daytime sleepiness in obese patients with childhood craniopharyngioma

First randomized multicenter study in patients with childhood craniopharyngioma analyzing the appropriate time point of irradiation after incomplete resection – study design of KRANIOPHARYNGEOM 2007

Spangenberg, P.

Successful continuous lumbar intrathecal interferon alpha treatment in SSPE

Sperner, J.

Vagus nerve stimulation and heart rate – the influence of vagus nerve stimulation output current on heart rate

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Tuberous Sclerosis Complex as a cause of prenatally diagnosed polycystic kidney disease

Spiczak, S. von

DYT11– Myoclonic Dystonia as a rare form of childhood dystonia

Springer, S.

Neuropediatric problems in child and adolescent psychiatry

Neuropsychological assessment of language and cognition in children with autistic disorders

Multiprofessional assessment and treatment of children with autistic disorders

Staudt, F.

PVL – A differentiation of various classifications

Interstitial deletion (2)(q11.2-q21) in a newborn with multiple malformations

First seizure as side effect of an enuresis therapy – a case report

Editorial

Thickening of the dura mater T3-T9– incidental finding or manifestation of neuroborreliosis?

Case report of a 13 year old girl with a congenital myasthenic syndrome (CMS), a long way to diagnosis

Subtelomeric findings in children with autistic behaviour: three case reports

Staudt, M.

Reorganization in congenital hemiparesis: fMRI activation of ipsilateral basal ganglia during paretic hand movement

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a fMRI study

Intracortical inhibition in patients suffering from congenital hemiparesis

Cerebellar activation in right-hemispheric language dominance following early left-sided brain lesions

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

(Re-)organization of sensorimotor and language functions after periventricular lesions

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a TMS study

Stein, S.

Constraint-Induced Movement Therapy (CIMT) in patients with congenital hemiparesis: Differences between two groups of patients, one with controlateral, one with ipsilateral cortico-spinal reorganisation

Validity and responsiveness of the GMFM-66 for children and adolescents with traumatic brain injury

Steinhoff, B. J.

Factors influencing surgical outcome in patients with focal cortical dysplasia

Steinlin, M.

Reactivation of bilateral cognitive networks after stroke in childhood

Diagnostic errors in shunt dysfunction

Stenger, R. D.

Loss of vertical gaze – the Parinaud syndrome

Stephani, U.

KCNQ3 and KCNQ2 mutations contribute to rare and common forms of idiopathic epilepsy

Inspiratory muscle load during stenotic breathing in children with neuromuscular diseases

DYT11– Myoclonic Dystonia as a rare form of childhood dystonia

Stettner, G. M.

Treatment of epilepsy in patients with Rett syndrome

Stienen, A.

Neurological manifestations of EBV infection: a heterogeneous disease entity

Stoffel-Wagner, B.

Reduced sympathetic metabolites in urine of obese patients with craniopharyngioma

Cerebrospinal fluid obstruction and CSF malresorption: Analysis of specific CSF biomarkers indicative for growth factor- and fibrosis- related CSF malabsorption in neonatal hydrocephalus

Stoltenburg-Dindinger, G.

Magnetic resonance imaging of skeletal muscles reveals a distinct pattern of muscle involvement in a family with congenital myopathy caused by a RYR1 mutation

Stöver, B.

Decreased midbrain grey matter after prenatal exposure to antiepileptic drugs

Strahl, S.

Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K)

Strobl, K.

Factors influencing surgical outcome in patients with focal cortical dysplasia

Progressive leftsided cerebellar atrophy and intermittend CSWS-like EEG. Is it Rasmussen Encephalitis?

Zonisamide in refractory epilepsies of childood and adolescence

Strobl-Wildemann, G.

Interstitial deletion (2)(q11.2-q21) in a newborn with multiple malformations

Case report of a 13 year old girl with a congenital myasthenic syndrome (CMS), a long way to diagnosis

Subtelomeric findings in children with autistic behaviour: three case reports

Stülpnagel, C. von

No correlation for MDR1 polymorphisms and pharmacoresistent epilepsy in children

Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option?

Tacke, J.

Thickening of the dura mater T3-T9– incidental finding or manifestation of neuroborreliosis?

Tacke, U.

Relevance of abdominal fluid for the assessment of ventriculoperitoneal shunt function in children

Tatarczyk, T.

Effect of valproic acid treatment on body composition, leptin and soluble leptin receptor in epileptic children

Teelken, A.

Cerebrospinal fluid obstruction and CSF malresorption: Analysis of specific CSF biomarkers indicative for growth factor- and fibrosis- related CSF malabsorption in neonatal hydrocephalus

Teichmann, H.

Endoscopic cystoventriculostomy and ventriculocysternostomy using a recently developed 2.0 micron near infrared laser in patients with hydrocephalus

Teske, C.

Quality of life (QoL) in childhood craniopharyngioma – current status of the prospective multicenter study KRANIOPHARYNGEOM 2000 and results of a retrospective study on 185 long-term survivors

Thimm, A.

Progressive hearing loss as presenting symptom of benign intracranial hypertension

Thomann, P.

Effect of early intervention on infantile postural asymmetry: a prospective 2 years follow-up

Thurner, B.

Successful continuous lumbar intrathecal interferon alpha treatment in SSPE

Tibussek, D.

Seasonal clustering of prepubertal idiopathic intracranial hypertension

Successfull therapy with Rituximab in an adolescent patient with severe multiple sclerosis

Titze, K.

Decreased midbrain grey matter after prenatal exposure to antiepileptic drugs

Tolnay, M.

Pontine involvement as an imaging feature of severe hypoxic-ischemic encephalopathy in the term neonate

Tost, F.

Loss of vertical gaze – the Parinaud syndrome

Traus, M.

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Treiss, I.

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Trippel, M.

Efficacy of interstitial radiosurgery in the treatment of pharmacoresistant gelastic epilepsy due to hypothalamic hamartomas

Trollmann, R.

Acute encephalopathy as the presenting symptom in Henoch-Schoenlein purpura: A case report

3-methylglutaconic aciduria in mitochondrial encepahlopathy: 2 case reports

Tuxhorn, I.

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Efficacy of interstitial radiosurgery in the treatment of pharmacoresistant gelastic epilepsy due to hypothalamic hamartomas

Uhlenberg, B.

Clinical manifestations and neuroimaging in neuroborreliosis – an unexpectedly high portion of patients with cerebral arteriopathy

A new form of spinal muscular atrophy

Urbanek, M.

Pharmacological inhibition of NADPH oxidase does not reduce excitotoxic brain lesion in newborn mice

Granulocyte-Colony stimulating factor reduces brain injury in newborn mice when given after the acute phase of brain injury

Dextromethorphan an „old“ drug to protect the newborn brain against perinatal injury?

Utzig, N.

Neurophysiological correlatives of eating behavior in obese children and adolescents

Uyanik, G.

Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K)

Valente, E. M.

Failure of decussation of important pathways demonstrated by MR tractography in Joubert syndrome

Vavrik, K.

Psychotraumatology and trauma management in the neurorehabilitation

Veelken, N.

Trigeminal neuralgia in children – differential therapy and neurosurgical indication

Velthoven, V. van

Relevance of abdominal fluid for the assessment of ventriculoperitoneal shunt function in children

Villain, M.

Rare causes of hemicrania in childhood and youth

Visconti, P.

Microduplication 22Q11.2 in a child with autistic disorder: clinical and genetic study

Vlaho, S.

Cognitive long- term outcomes after acute lymphoblastic leukaemia in childhood

Does valproic acid cause cardiac arrhythmias, in particular QT-prolongations, as possible SUDEP risk factor?

Bilateral decompressive craniectomy in a predominantly hypoxic brain damage

Retrobulbar pain, diplopia and exophthalmus as manifestations of an isolated ocular myositis in a 15 year old boy

Posterior Reversible Encephalopathy Syndrome (PRES) in children – a single-institution retrosprective study

Primary pseudotumor cerebri in association with obesity – a rare differential diagnosis even in childhood

Voit, T.

Ubiquitin-Proteasome pathway alteration in distal myopathy due to a mutation in a novel kelch protein

Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K)

Vry, J.

Integrity of the corticospinal system in children with bilateral cerebral palsy and periventricular leukomalacia: A transcranial magnetic stimulation study

Validity and responsiveness of the GMFM-66 for children and adolescents with traumatic brain injury

Vuksic, M.

The structural basis of developmental plasticity in the human brain

Wagner, K.

Neurophysiological correlatives of eating behavior in obese children and adolescents

Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma

Wagner, N.

Intracortical inhibition in patients suffering from congenital hemiparesis

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a TMS study

Wagner, S.

Mind and behaviour in children and young adults with monotherapy of the antipeleptic drugs valproic acid, carbamazepine and sultiam

Waldegger, S.

KCNQ3 and KCNQ2 mutations contribute to rare and common forms of idiopathic epilepsy

Walther, M.

An optimized scheme of motor learning

Intracortical inhibition in patients suffering from congenital hemiparesis

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a TMS study

Validity and responsiveness of the GMFM-66 for children and adolescents with traumatic brain injury

Wang, S.

Randomized dose-controlled multicenter study of topiramate as first line therapy in adolescents with epilepsy

Warmuth-Metz, M.

High rates of early relapses after complete resection and early tumor progressions after incomplete resection of childhood craniopharyngioma – update after three years of prospective evaluation in KRANIOPHARYNGEOM 2000

First randomized multicenter study in patients with childhood craniopharyngioma analyzing the appropriate time point of irradiation after incomplete resection – study design of KRANIOPHARYNGEOM 2007

Papillary hypothalamic tumour in a patient with tuberous sclerosis: A case report

Warnke, A.

Autism: diagnostic Questions and the clinic Picture

Weber, P.

Mismatch detection: an auditory event-related study to detect differences in pre-attentive and learning capability of fullterm and preterm newborns

Weber, V.

Relevance of abdominal fluid for the assessment of ventriculoperitoneal shunt function in children

Weger, C.

Therapy with ACTH versus pulsatile corticoid – retrospective analysis of efficacy in treatment of infantile epilepsy syndromes

Wegleiter, K.

Granulocyte-Colony stimulating factor reduces brain injury in newborn mice when given after the acute phase of brain injury

Weiller, C.

Detection of a KRAS Mutation in a Pilocytic Astrocytoma

Weimann, E.

Follow-up of tuberous sclerosis in 3 year-old boy – a case report

Weis, R.

The rule of methylphenidate in the treatment of autism

Is less more? Trend of epileptic seizures and behavior in a TSC 1 patient with and without anticonvulsant treatment

Tuberous Sclerosis with deletion on chromosome 9q and TSC-2-like brain dysplasia but TSC 1- like outcome: a case report

Smith-Magenis syndrome: a case report of improved sleep after treatment with atomoxetin and melatonin

Weiss, C.

Clinical manifestations and neuroimaging in neuroborreliosis – an unexpectedly high portion of patients with cerebral arteriopathy

Weiss, S.

Double Trouble: A clinical, molecular genetic mixed type of FSHD and Selenoprotein N rigid spine syndrome as a „new“ neuromuscular disease

Weiß, B.

Idiopathic intracranial hypertension – a review over 16 cases in childhood

Weissenmayer, H.

Validity and responsiveness of the GMFM-66 for children and adolescents with traumatic brain injury

Weithmann, L.

Case report of a 13 year old girl with a congenital myasthenic syndrome (CMS), a long way to diagnosis

Weltzien, A.

Distal phalanx necrosis after intra-arterial injection of phenobarbital during treatment of subtle generalized convulsive status epilepticus

Wenning, G.

Pharmacological inhibition of NADPH oxidase does not reduce excitotoxic brain lesion in newborn mice

Wenzel, D.

Acute encephalopathy as the presenting symptom in Henoch-Schoenlein purpura: A case report

3-methylglutaconic aciduria in mitochondrial encepahlopathy: 2 case reports

A cerebral sinus thrombosis in a 4 year old child

Weschke, B.

Clinical manifestations and neuroimaging in neuroborreliosis – an unexpectedly high portion of patients with cerebral arteriopathy

Wesiger, S.

The 22q11 deletion syndrome poses a multidisciplinary challenge for pediatricians and child psychiatrists as shown by a case report

Wesley, E.

Ubiquitin-Proteasome pathway alteration in distal myopathy due to a mutation in a novel kelch protein

Wiberg, A.

Multiprofessional assessment and treatment of children with autistic disorders

Wiegand, F.

Randomized dose-controlled multicenter study of topiramate as first line therapy in adolescents with epilepsy

Wiemer-Kruel, A.

Progressive leftsided cerebellar atrophy and intermittend CSWS-like EEG. Is it Rasmussen Encephalitis?

Zonisamide in refractory epilepsies of childood and adolescence

Wienecke, R.

Non-neurological aspects of tuberous sclerosis

Wilhelm, T.

Decreased midbrain grey matter after prenatal exposure to antiepileptic drugs

Wilke, M.

Constraint-induced movement therapy in congenital hemiparesis with different types of cortico-spinal reorganization: a fMRI study

Cerebellar activation in right-hemispheric language dominance following early left-sided brain lesions

Reactivation of bilateral cognitive networks after stroke in childhood

Willig, B.

Monosymptomatic rheumatic fever – Chorea Sydenham

Winkler, P.

Imaging in Tuberous Sclerosis Complex (TSC) with particular consideration of cerebral abnormalities

Wolff, M.

17-year-old boy with atypical mild clinical course of Canavan disease

Wright, T.

Combined EEG and MEG analysis of early tactile evoked activity in patients with focal epilepsies

Wyttenbach, M.

Clinical manifestations of benign tectal glioma in children and adolescents

Yagmur, E.

Subaponeurotic fluid-collection after birth- a self limiting cerebrospinal fluid fistula?

Zagler, J.

The rule of methylphenidate in the treatment of autism

Zeitler, P.

X-linked hydrocephalus: Another family with a novel mutation in the L1CAM-gene

Zeller, M.

First seizure as side effect of an enuresis therapy – a case report

Zentner, J.

Factors influencing surgical outcome in patients with focal cortical dysplasia

Zill, P.

No correlation for MDR1 polymorphisms and pharmacoresistent epilepsy in children

Zimmer, B.

Is less more? Trend of epileptic seizures and behavior in a TSC 1 patient with and without anticonvulsant treatment

Zschocke, J.

Late diagnosis of pyridoxal- phosphate depending epilepsy: Case report of a 5 year old boy

Zsoter, A.

Menkes-Syndrome: Delayed diagnosis because of misinterpretation as battered child syndrome in 2 of 3 children in 2006

Long term use of zonisamide in refractory childhood-onset epilepsy

Sodium channel influencing drugs may provoke refractory status epilepticus in patients with SCN1A-mutations!