Abstracts of the 32nd Annual Meeting – of the Society for Neuropediatrics – (Gesellschaft für Neuropädiatrie)

Ahlbory, K.

Vagusnerve stimulation in paediatric epilepsy: Bethel experience 2000–2004

Good seizure outcome after epilepsy surgery in young children with tuberous sclerosis complex

Aksu, F.

FLIP&FLAP: Development and evaluation of a structured epilepsy education programme for children and adolescents with epilepsy and their parents

Albani, M.

Comparison of the disease course of two patients with SMARD1

Allmendinger, A.

Differential diagnosis of gelastic seizures beside hypothalamic hamartoma

Altenmüller, S.

Cognition and behaviour in children and young adults related to monotherapy with valproic acid, carbamazepine and sulthiam – First results

Appel-Ramb, C.

Retrospective study on intellectual and scholastic development of 10–18-year-old former patients with febrile convulsions in the anamnesis

On the biographical significance of simple and complex febrile convulsions in a sample of 10–18-year old former patients. A retrospective study concerning the question: does parental anxiety cause anxiety in children?

Armbruster, S.

Efficacy of levetiracetam in the treatment of children with BECTS. A prospective, open-label pilot trial prior to a controlled, randomised, double-blind German multicentre trial (HEAD-Study)

Arroyo, S.

Adjunctive therapy of rufinamide in patients with Lennox-Gastaut syndrome

Ashcroft, F. M.

Successful therapy with glibenclamid in a patient with a muation of KIR 6.2 subunit of the ATP-sensitive potassium channel

Assmann, B.

Mydriasis without reaction to light, normal vigilance and pharyngitis: an unusual disorder

Benign infantile convulsions associated with mild gastroenteritis. Case report and review of the literature

Auer-Grumbach, M.

Chronic inflammatory demyelinating polyradiculoneuropathy in children and adolescents-longterm follow-up in 7 patients

MuSK autoantibody positive myasthenia gravis in a 14 year old boy: difficulties in diagnosis and response to treatment with plasmapheresis and immunosuppression

Auth, M.

Biliary atresia as initial manifestation of Niemann Pick C1 disease

Bächli, H.

Intrathecal Baclofen therapy in children and young adults: first experience

Bahn, E.

Proinflammatory molecules such as IFN-gamma and iNOS are not expressed in 25F9 positive macrophages in dermatomyositis

Ballauf, A.

Biliary atresia as initial manifestation of Niemann Pick C1 disease

Bast, T.

Successful therapy with glibenclamid in a patient with a muation of KIR 6.2 subunit of the ATP-sensitive potassium channel

Epilepsies in mitochondrial disorders: seizure types and history

Benefit of vagal nerve stimulation in epilepsia partialis continua: a case report

Usefulness of combined MEG and voxel-based morphometric MRI analysis in cryptogenic frontal lobe epilepsy

Delayed middle-latency auditory-evoked fields in children with benign centrotemporal sharp-waves

Differential diagnosis of gelastic seizures beside hypothalamic hamartoma

Bauder, F.

Neonatal seizures: eyes open or closed?

Bauer, B.

Adjunctive therapy of rufinamide in patients with Lennox-Gastaut syndrome

Bauer, R.

Effects of therapeutic and toxic phenobarbital doses on brain tissue caspase 3-activity in the neonatal rat

Baumeister, F.

Atypical variant of Alexander's disease with involvement of the spinal cord

Baumgartner, B.

Efficacy of levetiracetam in the treatment of children with BECTS. A prospective, open-label pilot trial prior to a controlled, randomised, double-blind German multicentre trial (HEAD-Study)

Baz Bartels, M.

Fatal course of maple syrup urine disease (MSUD) encephalopathy in a 6 year old boy with characteristic MRI-changes

A rare progressive neurometabolic disease (L-2-hydroxyglutaric aciduria) diagnosed by urinary organic acid analysis

Difficulties in diagnosing progressive bulbar paralysis (Fazio-Londe disease)

Cranial metastasis of a 13-year-old patient with bronchial carcinoma

Effect of intrathecal methotrexate on biogenic amines in CSF of children and adolescents with acute lymphoblastic leukaemia enrolled in the ALL-BFM 2000 multicentre treatment study

Beck, S.

Surface-binding autoantibodies in childhood opsoclonus-myoclonus syndrome – binding and pathogenic effects of autoantibodies

Becker, H.

Atrophy of vermis cerebelli in Schimke-immuno-osseous dysplasia

Behmer, M.

Morbus Hallervorden-Spatz and atomoxetin: a therapeutic option?

Behne, F.

Vagusnerve stimulation in paediatric epilepsy: Bethel experience 2000–2004

Good seizure outcome after epilepsy surgery in young children with tuberous sclerosis complex

Developmental progress in paediatric temporal lobe epilepsy

Bell, N.

Oral rapid loading of valproic acid – an alternative to the usual

Valproic acid induced pancreatitis: 16 new cases and literature overview

Bendl, C.

Smith-Lemli-Opitz syndrome: case report on two patients with different clinical presentation

Cognition and behaviour in children and young adults related to monotherapy with valproic acid, carbamazepine and sulthiam – First results

Berger, A.

Differential diagnosis of gelastic seizures beside hypothalamic hamartoma

Berger, K.

Congenital facial palsy and peripheral neuropathy. Manifestation of Neurofibromatosis Type 2 in childhood

Bergmann, M.

Congenital myopathy with rigid spine caused by Selenoproteine 1- deficiency

Bernert, G.

Sleep-related central respiratory drive disorder in so far unidentified primary disease

Bernhard, M. K.

Toe-walking as the first presenting symptom of Emery-Dreifuss muscular dystrophy type 1

Low level trisomy 16 mosaicism causing psychomotor retardation, epilepsia, adipositas and clubbing feet in an 8-year old girl

Long-term out-come, epidemiology and seizure recurrence of children with epilepsy of the University of Leipzig

Psychosocial aspects after a first seizure for children and parents

Berweck, S.

Increased fMRI activation in the primary sensorimotor cortex (M1S1) after constraint induced movement therapy in congenital hemiparesis

Bettendorf, U.

Valproic acid induced pancreatitis: 16 new cases and literature overview

Betzler, C.

Deficits in motor planning after acute damage to the posterior part of the corpus callosum –3 case reports

Severe anterograde memory deficits post traumatic damage to the thalamus –2 case-reports

Bevot, A.

Development of preterm children with early postnatally-acquired cytomegalovirus infection via breast milk

Bien, C. G.

Benefit of vagal nerve stimulation in epilepsia partialis continua: a case report

Atypical Rasmussen-encephalitis with progressing hemiparesis and lacking seizures

Bier, A.

Epilepsy and mental retardation with a distinctive facial phenotype – diagnosis on the spot with moleculargenetic confirmation – Mowat-Wilson syndrome

Bigalke, H.

Regulation of respiratory chain in intact N. phrenicus-hemi-diaphragm

Bittner, R.

MuSK autoantibody positive myasthenia gravis in a 14 year old boy: difficulties in diagnosis and response to treatment with plasmapheresis and immunosuppression

Blaes, F.

Surface-binding autoantibodies in childhood opsoclonus-myoclonus syndrome – binding and pathogenic effects of autoantibodies

Blank, R.

SEMG-feedback can improve fine motor control in children with hemiparesis – Two case reports

Bliedtner, A.

Psychosocial aspects after a first seizure for children and parents

Bochennek, K.

Effect of intrathecal methotrexate on biogenic amines in CSF of children and adolescents with acute lymphoblastic leukaemia enrolled in the ALL-BFM 2000 multicentre treatment study

Boda, V.

Fatal course of maple syrup urine disease (MSUD) encephalopathy in a 6 year old boy with characteristic MRI-changes

A rare progressive neurometabolic disease (L-2-hydroxyglutaric aciduria) diagnosed by urinary organic acid analysis

Complex intracerebral malformation with large occipital encephalocele – diagnose and interdisciplinary management

Difficulties in diagnosing progressive bulbar paralysis (Fazio-Londe disease)

Cranial metastasis of a 13-year-old patient with bronchial carcinoma

Effect of intrathecal methotrexate on biogenic amines in CSF of children and adolescents with acute lymphoblastic leukaemia enrolled in the ALL-BFM 2000 multicentre treatment study

Boerkoel, C. F.

Atrophy of vermis cerebelli in Schimke-immuno-osseous dysplasia

Bogena, B.

Regulation of respiratory chain in intact N. phrenicus-hemi-diaphragm

Böhles, H.

Normal ventricular size in brain imaging does not exclude blockage of cerebrospinal fluid shunts

Boltshauser, E.

PEHO syndrome: well described but easily missed

Outcome of intraspinal tumours in children: long-term complications and quality of life

Outcome of brain tumour in children less than 1 year of age: long-term complications and quality of life

Sinus venous thrombosis in Swiss children

Bonfert, M.

Efficacy of levetiracetam in the treatment of children with BECTS. A prospective, open-label pilot trial prior to a controlled, randomised, double-blind German multicentre trial (HEAD-Study)

Borusiak, P.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Successful treatment of atypical idiopathic focal epilepsy with CSWS with levetiracetam

Bosch, F.

Cognition and behaviour in children and young adults related to monotherapy with valproic acid, carbamazepine and sulthiam – First results

Boscherini, D.

Spontaneous spinal epidural haematomas in children: can we prevent a bad evolution? Reflection on 2 cases

Boxtermann, W.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Brandl, U.

Effects of therapeutic and toxic phenobarbital doses on brain tissue caspase 3-activity in the neonatal rat

Brocke, K. S.

Progressive ataxia and symptomatic epilepsy in a case of leukoencephalopathy with brainstem and spinal cord involvement

Brockhaus, A.

Benign Idiopathic Focal Epileptiform Discharges of Childhood (BIFEDC) and Benign Idiopathic Focal Epilepsies of Childhood (BIFEC) in children with drug-ressistant symptomatic focal epilepsies

Brockmann, K.

Leigh syndrome: an uncommon manifestation caused by biotinidase-deficiency

Acute cerebellitis with fatal and near-fatal course

Motor neuropathy and alacrima: oligosymptomatic triple A syndrome

Valproic acid induced pancreatitis: 16 new cases and literature overview

Broxtermann, W.

Benefit of vagal nerve stimulation in epilepsia partialis continua: a case report

Brückner, H.

Usefulness of combined MEG and voxel-based morphometric MRI analysis in cryptogenic frontal lobe epilepsy

Brückner, R.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Brühl, K.

Interactive functional Doppler sonography reveals right-hemispheric language lateralization in children with left-sided cortical malformations

Brunner, R.

Intrathecal Baclofen therapy in children and young adults: first experience

Brunner-Krainz, M.

Congenital methemoglobinemia type II (RCM II): an inherited neurodegenerative disease

Chronic inflammatory demyelinating polyradiculoneuropathy in children and adolescents-longterm follow-up in 7 patients

Burtzlaff, C.

Severe mitochondrial disorder in spite of normal findings? Alpers syndrome due to homozygosity for A467T mutation in POLG gene

Busch, V.

Atypical variant of Alexander's disease with involvement of the spinal cord

Büsing, D.

Valproic acid induced pancreatitis: 16 new cases and literature overview

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Bussmann, C.

Benefit of vagal nerve stimulation in epilepsia partialis continua: a case report

Chen, C.

Mydriasis without reaction to light, normal vigilance and pharyngitis: an unusual disorder

Benign infantile convulsions associated with mild gastroenteritis. Case report and review of the literature

Christen, H. J.

Acute cerebellitis with fatal and near-fatal course

Cirak, S.

Biliary atresia as initial manifestation of Niemann Pick C1 disease

Clewing, J. M.

Atrophy of vermis cerebelli in Schimke-immuno-osseous dysplasia

Das, A. M.

Acute cerebellitis with fatal and near-fatal course

Atrophy of vermis cerebelli in Schimke-immuno-osseous dysplasia

Regulation of respiratory chain in intact N. phrenicus-hemi-diaphragm

Däublin, G.

Arteria spinalis anterior syndrome after visit of an amusement park with roller coaster rides

Debus, O. M.

Primary symptoms and their influence on the interval between symptom onset and diagnosis in pediatric brain tumours

Degen, I.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Degenhardt, V.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Denne, C.

Diagnostic impact of intrathecally synthesized specific anti-viral antibodies

Application of Cox regression analysis to identify perinatal risk factors for neurodevelopmental outcome

deVile, C.

Paroxysmal eating-induced dystonic choreoathetosis – a second case

Dieckhoefer, A.

Diagnostic impact of intrathecally synthesized specific anti-viral antibodies

Diers, A.

Macrocephaly in a 10-week-old infant: isolated symptom of a citrobacter encephalitis with intracranial abscesses

Dimitrios, C.

Assessment of the autonomic nervous system function in infants: the pupillary light reflex: normative data and physiological observations

Dittrich, S.

Fatal course of maple syrup urine disease (MSUD) encephalopathy in a 6 year old boy with characteristic MRI-changes

Successful anticonvulsive therapy with D/L 3-hydroxybutyrate and ketogenic diet in a boy with agininosccinate lyase deficiency and status epileptics minor

A rare progressive neurometabolic disease (L-2-hydroxyglutaric aciduria) diagnosed by urinary organic acid analysis

Complex intracerebral malformation with large occipital encephalocele – diagnose and interdisciplinary management

Effect of intrathecal methotrexate on biogenic amines in CSF of children and adolescents with acute lymphoblastic leukaemia enrolled in the ALL-BFM 2000 multicentre treatment study

Donnerstag, F.

Atrophy of vermis cerebelli in Schimke-immuno-osseous dysplasia

Dötsch, J.

Differential up-regulation of hypoxia-inducible vasoactive factors in fetal mouse brain in vivo upon intrauterine hypoxia

Droste, S.

Regulation of respiratory chain in intact N. phrenicus-hemi-diaphragm

Dutschmann, M.

Comparative studies on the respiratory dysfunction in Rett syndrome patients and the corresponding mouse model

Eber, E.

Congenital methemoglobinemia type II (RCM II): an inherited neurodegenerative disease

Ebinger, F.

Successful therapy with glibenclamid in a patient with a muation of KIR 6.2 subunit of the ATP-sensitive potassium channel

Acute chorea as leading symptom in systemic lupus erythomatosus

Epilepsies in mitochondrial disorders: seizure types and history

Eckel, U.

Valproic acid induced pancreatitis: 16 new cases and literature overview

Emmert, R.

Pelizaeus Merzbacher phenotype with epilepsy and autosomal recessive inheritance in two siblings

Ernst, J. P.

Usefulness of combined MEG and voxel-based morphometric MRI analysis in cryptogenic frontal lobe epilepsy

Fauser, S.

Usefulness of combined MEG and voxel-based morphometric MRI analysis in cryptogenic frontal lobe epilepsy

Feichtinger, M.

Stereotactic radiosurgery for hypothalamic hamartomas

Feldmann, E.

Cognition and behaviour in children and young adults related to monotherapy with valproic acid, carbamazepine and sulthiam – First results

Ferreiro, A.

Phenotype of children with congenital SEPN1-related myopathy and rigid spine

Fey-Engbert, M.

Morbus Hallervorden-Spatz and atomoxetin: a therapeutic option?

Fiedler, B. J.

Primary symptoms and their influence on the interval between symptom onset and diagnosis in pediatric brain tumours

Fink, H. S.

Effects of therapeutic and toxic phenobarbital doses on brain tissue caspase 3-activity in the neonatal rat

Fitzek, S.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Freisinger, P.

Atypical variant of Alexander's disease with involvement of the spinal cord

Clinical spectrum of polymerase-gamma mutation in 9 children

Freitag, H.

Vagusnerve stimulation in paediatric epilepsy: Bethel experience 2000–2004

Developmental progress in paediatric temporal lobe epilepsy

Friebel, D.

Epilepsy and mental retardation with a distinctive facial phenotype – diagnosis on the spot with moleculargenetic confirmation – Mowat-Wilson syndrome

Frischer, T.

Sleep-related central respiratory drive disorder in so far unidentified primary disease

Fuchs, U.

Successful therapy with glibenclamid in a patient with a muation of KIR 6.2 subunit of the ATP-sensitive potassium channel

Fühlhuber, V.

Surface-binding autoantibodies in childhood opsoclonus-myoclonus syndrome – binding and pathogenic effects of autoantibodies

Fütterer, N.

Clinical spectrum of polymerase-gamma mutation in 9 children

Gaiser, U.

Pelizaeus Merzbacher phenotype with epilepsy and autosomal recessive inheritance in two siblings

Gärtner, J.

Proinflammatory molecules such as IFN-gamma and iNOS are not expressed in 25F9 positive macrophages in dermatomyositis

Comparative studies on the respiratory dysfunction in Rett syndrome patients and the corresponding mouse model

Motor neuropathy and alacrima: oligosymptomatic triple A syndrome

Mitochondrial Myopathies in childhood and adolescence – Presentation, diagnosis und treatment

Identification of a novel inborn neurodegenerative disease of childhood: cathepsin D deficiency

Gassmann, M.

Differential up-regulation of hypoxia-inducible vasoactive factors in fetal mouse brain in vivo upon intrauterine hypoxia

Gebhardt, B.

Successful anticonvulsive therapy with D/L 3-hydroxybutyrate and ketogenic diet in a boy with agininosccinate lyase deficiency and status epileptics minor

A rare progressive neurometabolic disease (L-2-hydroxyglutaric aciduria) diagnosed by urinary organic acid analysis

L-Dopa/Carbidopa-therapy in children

Effect of intrathecal methotrexate on biogenic amines in CSF of children and adolescents with acute lymphoblastic leukaemia enrolled in the ALL-BFM 2000 multicentre treatment study

Gempel, K.

Mitochondrial Myopathies in childhood and adolescence – Presentation, diagnosis und treatment

Gerber, N. U.

Outcome of brain tumour in children less than 1 year of age: long-term complications and quality of life

Gerlach, R.

Complex intracerebral malformation with large occipital encephalocele – diagnose and interdisciplinary management

Normal ventricular size in brain imaging does not exclude blockage of cerebrospinal fluid shunts

Cranial metastasis of a 13-year-old patient with bronchial carcinoma

Gerstner, T.

Autonomic function in children and adolescents with neurogenic syncopes

Assessment of the autonomic nervous system function in infants: the pupillary light reflex: normative data and physiological observations

Maturation of the autonomic nervous system: differences in heart rate variability in premature vs. term infants

Capillary microscopy and hemorheology in children during antiepileptic monotherapy with carbamazepine and valproate

Oral rapid loading of valproic acid – an alternative to the usual

Valproic acid induced pancreatitis: 16 new cases and literature overview

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Cognition and behaviour in children and young adults related to monotherapy with valproic acid, carbamazepine and sulthiam – First results

Glauser, T.

Adjunctive therapy of rufinamide in patients with Lennox-Gastaut syndrome

Goelz, R.

Development of preterm children with early postnatally-acquired cytomegalovirus infection via breast milk

Golla, G.

Cognition and behaviour in children and young adults related to monotherapy with valproic acid, carbamazepine and sulthiam – First results

Groeschel, S.

Virchow-Robin spaces on magnetic resonance images: normative data and their association with diseases

Grotzer, M. A.

Outcome of intraspinal tumours in children: long-term complications and quality of life

Outcome of brain tumour in children less than 1 year of age: long-term complications and quality of life

Gruber-Sedlmayr, U.

Congenital methemoglobinemia type II (RCM II): an inherited neurodegenerative disease

Chronic inflammatory demyelinating polyradiculoneuropathy in children and adolescents-longterm follow-up in 7 patients

Grulich-Henn, J.

Successful therapy with glibenclamid in a patient with a muation of KIR 6.2 subunit of the ATP-sensitive potassium channel

Gubser, D.

Sinus venous thrombosis in Swiss children

Haberlandt, E.

Clinical spectrum of polymerase-gamma mutation in 9 children

Haenggeli, C.

Sinus venous thrombosis in Swiss children

Haensch, C.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Haeusler, M.

Diagnostic impact of intrathecally synthesized specific anti-viral antibodies

Application of Cox regression analysis to identify perinatal risk factors for neurodevelopmental outcome

Häger, S.

FLIP&FLAP: Development and evaluation of a structured epilepsy education programme for children and adolescents with epilepsy and their parents

Hagleitner, N.

Chameleon Moebius syndrome

Hahn, A.

Rapidly progressive moyamoya syndrome in a 19-month old girl with Bartonella henselae infection and Factor V Leiden mutation

Hahn, G.

Progressive ataxia and symptomatic epilepsy in a case of leukoencephalopathy with brainstem and spinal cord involvement

Progressive leucoencephalopathy with macrocephaly, optic atrophy, epileptic seizures, and primary ovarian dysfunction with relative preservation of cognitive functions

Partially thrombosed megadolichobasilar artery in an 8-year old child with recurrent episodes of somnolence

Phenotype of children with congenital SEPN1-related myopathy and rigid spine

Hameister, K.

Atypical Rasmussen-encephalitis with progressing hemiparesis and lacking seizures

Hamprecht, K.

Development of preterm children with early postnatally-acquired cytomegalovirus infection via breast milk

Hanefeld, F.

Leigh syndrome: an uncommon manifestation caused by biotinidase-deficiency

Valproic acid induced pancreatitis: 16 new cases and literature overview

Virchow-Robin spaces on magnetic resonance images: normative data and their association with diseases

Hanusch, R.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Hartmann, H.

Acute cerebellitis with fatal and near-fatal course

Atrophy of vermis cerebelli in Schimke-immuno-osseous dysplasia

Hartmann, M.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Hattersley, A. T.

Successful therapy with glibenclamid in a patient with a muation of KIR 6.2 subunit of the ATP-sensitive potassium channel

Häussermann, P.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Hebing, B.

Valproic acid induced pancreatitis: 16 new cases and literature overview

Heckel, M.

Rapidly progressive moyamoya syndrome in a 19-month old girl with Bartonella henselae infection and Factor V Leiden mutation

Heidinger, B.

Morbus Hallervorden-Spatz and atomoxetin: a therapeutic option?

Heinen, F.

Efficacy of levetiracetam in the treatment of children with BECTS. A prospective, open-label pilot trial prior to a controlled, randomised, double-blind German multicentre trial (HEAD-Study)

Herbertz, S.

Toe-walking as the first presenting symptom of Emery-Dreifuss muscular dystrophy type 1

Low level trisomy 16 mosaicism causing psychomotor retardation, epilepsia, adipositas and clubbing feet in an 8-year old girl

Psychosocial aspects after a first seizure for children and parents

Herwig, J.

Fatal course of maple syrup urine disease (MSUD) encephalopathy in a 6 year old boy with characteristic MRI-changes

Heubner, G.

Progressive ataxia and symptomatic epilepsy in a case of leukoencephalopathy with brainstem and spinal cord involvement

Hillebrand, M.

Identification of a novel inborn neurodegenerative disease of childhood: cathepsin D deficiency

Hobbiebrunken, E.

Mitochondrial Myopathies in childhood and adolescence – Presentation, diagnosis und treatment

Hoffmann, R.

Valproic acid induced pancreatitis: 16 new cases and literature overview

Holthausen, H.

Benign Idiopathic Focal Epileptiform Discharges of Childhood (BIFEDC) and Benign Idiopathic Focal Epilepsies of Childhood (BIFEC) in children with drug-ressistant symptomatic focal epilepsies

Fast titration of adjunctive topiramate in paediatric patients with difficult-to-treat epilepsy

Deficits in motor planning after acute damage to the posterior part of the corpus callosum –3 case reports

Severe anterograde memory deficits post traumatic damage to the thalamus –2 case-reports

Hoppen, T.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Hörnchen, H.

Application of Cox regression analysis to identify perinatal risk factors for neurodevelopmental outcome

Hörster, F.

Successful therapy with glibenclamid in a patient with a muation of KIR 6.2 subunit of the ATP-sensitive potassium channel

Horvath, R.

Severe mitochondrial disorder in spite of normal findings? Alpers syndrome due to homozygosity for A467T mutation in POLG gene

Clinical spectrum of polymerase-gamma mutation in 9 children

Howell, T.

Indication and outcome of decompressive craniectomy of 6 children and teenagers with not conservative influenced posttraumatic cerebral swelling

Hübner, A.

Progressive leucoencephalopathy with macrocephaly, optic atrophy, epileptic seizures, and primary ovarian dysfunction with relative preservation of cognitive functions

Motor neuropathy and alacrima: oligosymptomatic triple A syndrome

Huebner, C.

Comparison of the disease course of two patients with SMARD1

Huehn, R.

Intracranial hypotension synodome – a rare cause of postural headache

Huismann, T.

PEHO syndrome: well described but easily missed

Huneus, U.

Morbus Hallervorden-Spatz and atomoxetin: a therapeutic option?

Huppertz, H. J.

Usefulness of combined MEG and voxel-based morphometric MRI analysis in cryptogenic frontal lobe epilepsy

Huppke, P.

Comparative studies on the respiratory dysfunction in Rett syndrome patients and the corresponding mouse model

Husain, R.

Effects of therapeutic and toxic phenobarbital doses on brain tissue caspase 3-activity in the neonatal rat

Ikonomidou, C.

Partially thrombosed megadolichobasilar artery in an 8-year old child with recurrent episodes of somnolence

Ikonomidou, H.

Progressive leucoencephalopathy with macrocephaly, optic atrophy, epileptic seizures, and primary ovarian dysfunction with relative preservation of cognitive functions

Illerhaus, M.

Morbus Hallervorden-Spatz and atomoxetin: a therapeutic option?

Illsinger, S.

Regulation of respiratory chain in intact N. phrenicus-hemi-diaphragm

Jansma, C.

Atypical Rasmussen-encephalitis with progressing hemiparesis and lacking seizures

Jantzen, S.

FLIP&FLAP: Development and evaluation of a structured epilepsy education programme for children and adolescents with epilepsy and their parents

Jenke, A.

Successful treatment of atypical idiopathic focal epilepsy with CSWS with levetiracetam

Jungck, A.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Jünger, C. H.

Increased fMRI activation in the primary sensorimotor cortex (M1S1) after constraint induced movement therapy in congenital hemiparesis

Kaindl, A.

Macrocephaly in a 10-week-old infant: isolated symptom of a citrobacter encephalitis with intracranial abscesses

Phenotype of children with congenital SEPN1-related myopathy and rigid spine

Kammerer, E.

Retrospective study on intellectual and scholastic development of 10–18-year-old former patients with febrile convulsions in the anamnesis

On the biographical significance of simple and complex febrile convulsions in a sample of 10–18-year old former patients. A retrospective study concerning the question: does parental anxiety cause anxiety in children?

Kaps, M.

Surface-binding autoantibodies in childhood opsoclonus-myoclonus syndrome – binding and pathogenic effects of autoantibodies

Karagiannopoulou, S.

Benign paroxysmal vertigo and migraine in children: epidemiological evidence

Prognostic markers for multiple febrile seizure recurrences

Karall, D.

Clinical spectrum of polymerase-gamma mutation in 9 children

Karch, D.

Editorial

Karenfort, M.

Benign infantile convulsions associated with mild gastroenteritis. Case report and review of the literature

Shuddering attacks as an important differential diagnosis of infantile epilepsy. A video-EEG presentation

Karremann, M.

Intracranial hypotension synodome – a rare cause of postural headache

Kasper, J. M.

Valproic acid induced pancreatitis: 16 new cases and literature overview

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Kaufmann, F.

Sinus venous thrombosis in Swiss children

Kehrli, P.

Spontaneous spinal epidural haematomas in children: can we prevent a bad evolution? Reflection on 2 cases

Keilmann, A.

Interactive functional Doppler sonography reveals right-hemispheric language lateralization in children with left-sided cortical malformations

Keller, E.

Sinus venous thrombosis in Swiss children

Kieslich, M.

Fatal course of maple syrup urine disease (MSUD) encephalopathy in a 6 year old boy with characteristic MRI-changes

Successful anticonvulsive therapy with D/L 3-hydroxybutyrate and ketogenic diet in a boy with agininosccinate lyase deficiency and status epileptics minor

A rare progressive neurometabolic disease (L-2-hydroxyglutaric aciduria) diagnosed by urinary organic acid analysis

Complex intracerebral malformation with large occipital encephalocele – diagnose and interdisciplinary management

Difficulties in diagnosing progressive bulbar paralysis (Fazio-Londe disease)

Normal ventricular size in brain imaging does not exclude blockage of cerebrospinal fluid shunts

Cranial metastasis of a 13-year-old patient with bronchial carcinoma

Effect of intrathecal methotrexate on biogenic amines in CSF of children and adolescents with acute lymphoblastic leukaemia enrolled in the ALL-BFM 2000 multicentre treatment study

Kiess, W.

Low level trisomy 16 mosaicism causing psychomotor retardation, epilepsia, adipositas and clubbing feet in an 8-year old girl

Kirsten, A.

Surface-binding autoantibodies in childhood opsoclonus-myoclonus syndrome – binding and pathogenic effects of autoantibodies

Klein, C.

Complex intracerebral malformation with large occipital encephalocele – diagnose and interdisciplinary management

Kleines, M.

Diagnostic impact of intrathecally synthesized specific anti-viral antibodies

Kleist-Welch Guerra, W.

Indication and outcome of decompressive craniectomy of 6 children and teenagers with not conservative influenced posttraumatic cerebral swelling

Klepper, J.

Biliary atresia as initial manifestation of Niemann Pick C1 disease

Klostermann, W.

Valproic acid induced pancreatitis: 16 new cases and literature overview

Kluger, G.

Benign Idiopathic Focal Epileptiform Discharges of Childhood (BIFEDC) and Benign Idiopathic Focal Epilepsies of Childhood (BIFEC) in children with drug-ressistant symptomatic focal epilepsies

Fast titration of adjunctive topiramate in paediatric patients with difficult-to-treat epilepsy

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Adjunctive therapy of rufinamide in patients with Lennox-Gastaut syndrome

Klusmann, A.

Paroxysmal eating-induced dystonic choreoathetosis – a second case

Knapp, R.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Knauer-Fischer, S.

Mydriasis without reaction to light, normal vigilance and pharyngitis: an unusual disorder

Knauth, M.

Atrophy of vermis cerebelli in Schimke-immuno-osseous dysplasia

Koch, H. G.

Mitochondrial Myopathies in childhood and adolescence – Presentation, diagnosis und treatment

Koch, J.

Clinical spectrum of polymerase-gamma mutation in 9 children

Koehler, K.

Motor neuropathy and alacrima: oligosymptomatic triple A syndrome

Kohl, B.

Differential diagnosis of gelastic seizures beside hypothalamic hamartoma

Köhler, G.

Morbus Hallervorden-Spatz and atomoxetin: a therapeutic option?

Kohlschütter, A.

Progressive ataxia and symptomatic epilepsy in a case of leukoencephalopathy with brainstem and spinal cord involvement

König, S.

Smith-Lemli-Opitz syndrome: case report on two patients with different clinical presentation

Autonomic function in children and adolescents with neurogenic syncopes

Assessment of the autonomic nervous system function in infants: the pupillary light reflex: normative data and physiological observations

Maturation of the autonomic nervous system: differences in heart rate variability in premature vs. term infants

Capillary microscopy and hemorheology in children during antiepileptic monotherapy with carbamazepine and valproate

Oral rapid loading of valproic acid – an alternative to the usual

Valproic acid induced pancreatitis: 16 new cases and literature overview

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Cognition and behaviour in children and young adults related to monotherapy with valproic acid, carbamazepine and sulthiam – First results

Königs, I.

Smith-Lemli-Opitz syndrome: case report on two patients with different clinical presentation

Kontopoulos, E.

Prognostic markers for multiple febrile seizure recurrences

Korenke, G. C.

Congenital myopathy with rigid spine caused by Selenoproteine 1- deficiency

Arteria spinalis anterior syndrome after visit of an amusement park with roller coaster rides

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Korinthenberg, R.

Validity of the Gross Motor Function Measure in children and adolescents with traumatic brain injury

Koutsobelis, D.

Electroencephalographical findings by Chiari malformation syndrome

Krägeloh-Mann, I.

Development of preterm children with early postnatally-acquired cytomegalovirus infection via breast milk

Krahn-Peper, C.

Vagusnerve stimulation in paediatric epilepsy: Bethel experience 2000–2004

Good seizure outcome after epilepsy surgery in young children with tuberous sclerosis complex

Developmental progress in paediatric temporal lobe epilepsy

Krasenbrink, I.

Surface-binding autoantibodies in childhood opsoclonus-myoclonus syndrome – binding and pathogenic effects of autoantibodies

Krauss, G.

Adjunctive therapy of rufinamide in patients with Lennox-Gastaut syndrome

Kress, W.

Congenital myopathy with rigid spine caused by Selenoproteine 1- deficiency

Krisl, T.

FLIP&FLAP: Development and evaluation of a structured epilepsy education programme for children and adolescents with epilepsy and their parents

Kroisel, P.

Mental retardation in a girl with a subtelomeric 20q deletion and loss of the myelin transcription factor 1 (MYT1)

Kröll, J.

PEHO syndrome: well described but easily missed

Kröpfl, T.

Mental retardation in a girl with a subtelomeric 20q deletion and loss of the myelin transcription factor 1 (MYT1)

Krumbholz, M.

Motor neuropathy and alacrima: oligosymptomatic triple A syndrome

Kuhn, H.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Kujat, A.

Low level trisomy 16 mosaicism causing psychomotor retardation, epilepsia, adipositas and clubbing feet in an 8-year old girl

Kunze, V.

Arteria spinalis anterior syndrome after visit of an amusement park with roller coaster rides

Kurlemann, G.

Retrospective study on intellectual and scholastic development of 10–18-year-old former patients with febrile convulsions in the anamnesis

On the biographical significance of simple and complex febrile convulsions in a sample of 10–18-year old former patients. A retrospective study concerning the question: does parental anxiety cause anxiety in children?

Primary symptoms and their influence on the interval between symptom onset and diagnosis in pediatric brain tumours

Kurth, C.

Usefulness of combined MEG and voxel-based morphometric MRI analysis in cryptogenic frontal lobe epilepsy

Kutschke, G.

Interactive functional Doppler sonography reveals right-hemispheric language lateralization in children with left-sided cortical malformations

Lang, K.

Effects of therapeutic and toxic phenobarbital doses on brain tissue caspase 3-activity in the neonatal rat

Lang-Dullenkopf, A.

Intrathecal Baclofen therapy in children and young adults: first experience

Lauffer, H.

Severe mitochondrial disorder in spite of normal findings? Alpers syndrome due to homozygosity for A467T mutation in POLG gene

Clinical spectrum of polymerase-gamma mutation in 9 children

Lee-Kirsch, M. A.

Epilepsy and mental retardation with a distinctive facial phenotype – diagnosis on the spot with moleculargenetic confirmation – Mowat-Wilson syndrome

Lehmann, A. C.

Indication and outcome of decompressive craniectomy of 6 children and teenagers with not conservative influenced posttraumatic cerebral swelling

Lehrnbecher, T.

Effect of intrathecal methotrexate on biogenic amines in CSF of children and adolescents with acute lymphoblastic leukaemia enrolled in the ALL-BFM 2000 multicentre treatment study

Lenz, T.

Autonomic function in children and adolescents with neurogenic syncopes

Assessment of the autonomic nervous system function in infants: the pupillary light reflex: normative data and physiological observations

Maturation of the autonomic nervous system: differences in heart rate variability in premature vs. term infants

Linder-Lucht, M.

Increased fMRI activation in the primary sensorimotor cortex (M1S1) after constraint induced movement therapy in congenital hemiparesis

Validity of the Gross Motor Function Measure in children and adolescents with traumatic brain injury

Lindmayer, F.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Longin, E.

Autonomic function in children and adolescents with neurogenic syncopes

Assessment of the autonomic nervous system function in infants: the pupillary light reflex: normative data and physiological observations

Maturation of the autonomic nervous system: differences in heart rate variability in premature vs. term infants

Oral rapid loading of valproic acid – an alternative to the usual

Valproic acid induced pancreatitis: 16 new cases and literature overview

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Lücke, T.

Acute cerebellitis with fatal and near-fatal course

Atrophy of vermis cerebelli in Schimke-immuno-osseous dysplasia

Regulation of respiratory chain in intact N. phrenicus-hemi-diaphragm

Lütjen, S.

Deficits in motor planning after acute damage to the posterior part of the corpus callosum –3 case reports

Severe anterograde memory deficits post traumatic damage to the thalamus –2 case-reports

Lütschg, J.

Sinus venous thrombosis in Swiss children

Maag, S.

Application of Cox regression analysis to identify perinatal risk factors for neurodevelopmental outcome

Mache, C.

Chronic inflammatory demyelinating polyradiculoneuropathy in children and adolescents-longterm follow-up in 7 patients

Macke, K.

Cerebral palsy covers Segawa syndrome

Maier, O.

Brainstem auditory evoked potentials in the diagnosis of congenital hearing impairment

Mall, V.

Increased fMRI activation in the primary sensorimotor cortex (M1S1) after constraint induced movement therapy in congenital hemiparesis

Validity of the Gross Motor Function Measure in children and adolescents with traumatic brain injury

Marcoz, J.

Sinus venous thrombosis in Swiss children

Marquardt, I.

Congenital myopathy with rigid spine caused by Selenoproteine 1- deficiency

Arteria spinalis anterior syndrome after visit of an amusement park with roller coaster rides

Martin, E.

PEHO syndrome: well described but easily missed

Marton, M. A.

SEMG-feedback can improve fine motor control in children with hemiparesis – Two case reports

Mayatepek, E.

Congenital facial palsy and peripheral neuropathy. Manifestation of Neurofibromatosis Type 2 in childhood

Mydriasis without reaction to light, normal vigilance and pharyngitis: an unusual disorder

Benign infantile convulsions associated with mild gastroenteritis. Case report and review of the literature

Shuddering attacks as an important differential diagnosis of infantile epilepsy. A video-EEG presentation

Mayr, J. A.

Clinical spectrum of polymerase-gamma mutation in 9 children

Meinck, H. M.

Benefit of vagal nerve stimulation in epilepsia partialis continua: a case report

Merkenschlager, A.

Toe-walking as the first presenting symptom of Emery-Dreifuss muscular dystrophy type 1

Low level trisomy 16 mosaicism causing psychomotor retardation, epilepsia, adipositas and clubbing feet in an 8-year old girl

Long-term out-come, epidemiology and seizure recurrence of children with epilepsy of the University of Leipzig

Psychosocial aspects after a first seizure for children and parents

Merkle, B.

Effects of therapeutic and toxic phenobarbital doses on brain tissue caspase 3-activity in the neonatal rat

Merz, U.

Application of Cox regression analysis to identify perinatal risk factors for neurodevelopmental outcome

Michaelis, U.

Validity of the Gross Motor Function Measure in children and adolescents with traumatic brain injury

Müller, J. U.

Indication and outcome of decompressive craniectomy of 6 children and teenagers with not conservative influenced posttraumatic cerebral swelling

Müller-Deile, A.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Müller-Felber, W.

Clinical spectrum of polymerase-gamma mutation in 9 children

Müller-Godeffroy, E.

FLIP&FLAP: Development and evaluation of a structured epilepsy education programme for children and adolescents with epilepsy and their parents

Neubauer, B.

Rapidly progressive moyamoya syndrome in a 19-month old girl with Bartonella henselae infection and Factor V Leiden mutation

Neuberger, J.

Pelizaeus Merzbacher phenotype with epilepsy and autosomal recessive inheritance in two siblings

Neumann, F. W.

Valproic acid induced pancreatitis: 16 new cases and literature overview

Nitsche, M.

Effect of intrathecal methotrexate on biogenic amines in CSF of children and adolescents with acute lymphoblastic leukaemia enrolled in the ALL-BFM 2000 multicentre treatment study

Oberman, B.

Interactive functional Doppler sonography reveals right-hemispheric language lateralization in children with left-sided cortical malformations

Oehring, R.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Oeverink, R.

Arteria spinalis anterior syndrome after visit of an amusement park with roller coaster rides

Oh, J.

Acute chorea as leading symptom in systemic lupus erythomatosus

Othmer, V.

Validity of the Gross Motor Function Measure in children and adolescents with traumatic brain injury

Pälmke, M.

Retrospective study on intellectual and scholastic development of 10–18-year-old former patients with febrile convulsions in the anamnesis

On the biographical significance of simple and complex febrile convulsions in a sample of 10–18-year old former patients. A retrospective study concerning the question: does parental anxiety cause anxiety in children?

Pannek, H.

Vagusnerve stimulation in paediatric epilepsy: Bethel experience 2000–2004

Good seizure outcome after epilepsy surgery in young children with tuberous sclerosis complex

Developmental progress in paediatric temporal lobe epilepsy

Panteliadis, C.

Benign paroxysmal vertigo and migraine in children: epidemiological evidence

Prognostic markers for multiple febrile seizure recurrences

Parbel, S.

Fatal course of maple syrup urine disease (MSUD) encephalopathy in a 6 year old boy with characteristic MRI-changes

Successful anticonvulsive therapy with D/L 3-hydroxybutyrate and ketogenic diet in a boy with agininosccinate lyase deficiency and status epileptics minor

A rare progressive neurometabolic disease (L-2-hydroxyglutaric aciduria) diagnosed by urinary organic acid analysis

Complex intracerebral malformation with large occipital encephalocele – diagnose and interdisciplinary management

Difficulties in diagnosing progressive bulbar paralysis (Fazio-Londe disease)

Normal ventricular size in brain imaging does not exclude blockage of cerebrospinal fluid shunts

Cranial metastasis of a 13-year-old patient with bronchial carcinoma

Effect of intrathecal methotrexate on biogenic amines in CSF of children and adolescents with acute lymphoblastic leukaemia enrolled in the ALL-BFM 2000 multicentre treatment study

Pavlidou, E.

Benign paroxysmal vertigo and migraine in children: epidemiological evidence

Prognostic markers for multiple febrile seizure recurrences

Pavlovic, J.

Sinus venous thrombosis in Swiss children

Percy, M. J.

Congenital methemoglobinemia type II (RCM II): an inherited neurodegenerative disease

Petek, E.

Mental retardation in a girl with a subtelomeric 20q deletion and loss of the myelin transcription factor 1 (MYT1)

Peters, C.

Cognition and behaviour in children and young adults related to monotherapy with valproic acid, carbamazepine and sulthiam – First results

Peters, H.

Cerebral palsy covers Segawa syndrome

Petrova, S.

Severe anterograde memory deficits post traumatic damage to the thalamus –2 case-reports

Pfander, T.

Proinflammatory molecules such as IFN-gamma and iNOS are not expressed in 25F9 positive macrophages in dermatomyositis

Pfleger, A.

MuSK autoantibody positive myasthenia gravis in a 14 year old boy: difficulties in diagnosis and response to treatment with plasmapheresis and immunosuppression

Pieper, T.

Benign Idiopathic Focal Epileptiform Discharges of Childhood (BIFEDC) and Benign Idiopathic Focal Epilepsies of Childhood (BIFEC) in children with drug-ressistant symptomatic focal epilepsies

Pietz, J.

Delayed middle-latency auditory-evoked fields in children with benign centrotemporal sharp-waves

Plecko, B.

Congenital methemoglobinemia type II (RCM II): an inherited neurodegenerative disease

Chronic inflammatory demyelinating polyradiculoneuropathy in children and adolescents-longterm follow-up in 7 patients

Mental retardation in a girl with a subtelomeric 20q deletion and loss of the myelin transcription factor 1 (MYT1)

Clinical spectrum of polymerase-gamma mutation in 9 children

MuSK autoantibody positive myasthenia gravis in a 14 year old boy: difficulties in diagnosis and response to treatment with plasmapheresis and immunosuppression

Poggenburg, I.

Arteria spinalis anterior syndrome after visit of an amusement park with roller coaster rides

Pohl, D.

Leigh syndrome: an uncommon manifestation caused by biotinidase-deficiency

Polster, T.

Comparison of the disease course of two patients with SMARD1

Pomarino, D.

Toe-walking as the first presenting symptom of Emery-Dreifuss muscular dystrophy type 1

Poretti, A.

Outcome of intraspinal tumours in children: long-term complications and quality of life

Porto, L.

Fatal course of maple syrup urine disease (MSUD) encephalopathy in a 6 year old boy with characteristic MRI-changes

Normal ventricular size in brain imaging does not exclude blockage of cerebrospinal fluid shunts

Cranial metastasis of a 13-year-old patient with bronchial carcinoma

Posselt, S.

A rare progressive neurometabolic disease (L-2-hydroxyglutaric aciduria) diagnosed by urinary organic acid analysis

Preiß, U.

Intracranial hypotension synodome – a rare cause of postural headache

Püst, B.

FLIP&FLAP: Development and evaluation of a structured epilepsy education programme for children and adolescents with epilepsy and their parents

Quasthoff, S.

Chronic inflammatory demyelinating polyradiculoneuropathy in children and adolescents-longterm follow-up in 7 patients

Raikhman, P.

Complex intracerebral malformation with large occipital encephalocele – diagnose and interdisciplinary management

Difficulties in diagnosing progressive bulbar paralysis (Fazio-Londe disease)

Ramantani, G.

Progressive leucoencephalopathy with macrocephaly, optic atrophy, epileptic seizures, and primary ovarian dysfunction with relative preservation of cognitive functions

Ramelli, G. P.

Spontaneous spinal epidural haematomas in children: can we prevent a bad evolution? Reflection on 2 cases

Rascher, W.

Differential up-regulation of hypoxia-inducible vasoactive factors in fetal mouse brain in vivo upon intrauterine hypoxia

Rating, D.

Successful therapy with glibenclamid in a patient with a muation of KIR 6.2 subunit of the ATP-sensitive potassium channel

Acute chorea as leading symptom in systemic lupus erythomatosus

Epilepsies in mitochondrial disorders: seizure types and history

Benefit of vagal nerve stimulation in epilepsia partialis continua: a case report

Usefulness of combined MEG and voxel-based morphometric MRI analysis in cryptogenic frontal lobe epilepsy

Delayed middle-latency auditory-evoked fields in children with benign centrotemporal sharp-waves

Differential diagnosis of gelastic seizures beside hypothalamic hamartoma

Rauscher-Lacher, H.

Development of preterm children with early postnatally-acquired cytomegalovirus infection via breast milk

Rauter, L.

Clinical spectrum of polymerase-gamma mutation in 9 children

Regel, E.

Pelizaeus Merzbacher phenotype with epilepsy and autosomal recessive inheritance in two siblings

Reinhard, J. E.

Autonomic function in children and adolescents with neurogenic syncopes

Reinhardt, K.

Identification of a novel inborn neurodegenerative disease of childhood: cathepsin D deficiency

Reitter, B.

Interactive functional Doppler sonography reveals right-hemispheric language lateralization in children with left-sided cortical malformations

Reulecke, B. C.

Primary symptoms and their influence on the interval between symptom onset and diagnosis in pediatric brain tumours

Richard, H.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Richard, P.

Phenotype of children with congenital SEPN1-related myopathy and rigid spine

Riedel, J.

Acute cerebellitis with fatal and near-fatal course

Ries, M.

Pelizaeus Merzbacher phenotype with epilepsy and autosomal recessive inheritance in two siblings

Rilliet, B.

Spontaneous spinal epidural haematomas in children: can we prevent a bad evolution? Reflection on 2 cases

Ritter, K.

Diagnostic impact of intrathecally synthesized specific anti-viral antibodies

Rödl, S.

Chronic inflammatory demyelinating polyradiculoneuropathy in children and adolescents-longterm follow-up in 7 patients

MuSK autoantibody positive myasthenia gravis in a 14 year old boy: difficulties in diagnosis and response to treatment with plasmapheresis and immunosuppression

Roll, K.

Deficits in motor planning after acute damage to the posterior part of the corpus callosum –3 case reports

Severe anterograde memory deficits post traumatic damage to the thalamus –2 case-reports

Romein, E.

Deficits in motor planning after acute damage to the posterior part of the corpus callosum –3 case reports

Röschinger, W.

Clinical spectrum of polymerase-gamma mutation in 9 children

Rose, M.

Cranial metastasis of a 13-year-old patient with bronchial carcinoma

Rosewich, H.

Acute cerebellitis with fatal and near-fatal course

Rostasy, K.

Proinflammatory molecules such as IFN-gamma and iNOS are not expressed in 25F9 positive macrophages in dermatomyositis

Roulet, E.

Sinus venous thrombosis in Swiss children

Rüdisser, K.

Atypical variant of Alexander's disease with involvement of the spinal cord

Rüggeberg, J.

Benign infantile convulsions associated with mild gastroenteritis. Case report and review of the literature

Rühl, M.

Cerebral palsy covers Segawa syndrome

Rupp, A.

Delayed middle-latency auditory-evoked fields in children with benign centrotemporal sharp-waves

Rustenbeck, H. H.

Leigh syndrome: an uncommon manifestation caused by biotinidase-deficiency

Sachdeo, R.

Adjunctive therapy of rufinamide in patients with Lennox-Gastaut syndrome

Sälke-Kellermann, R. A.

PEHO syndrome: well described but easily missed

Salomons, G. S.

Atypical variant of Alexander's disease with involvement of the spinal cord

Samii, K.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Sandrieser, T.

Valproic acid induced pancreatitis: 16 new cases and literature overview

Saxe, S.

Efficacy of levetiracetam in the treatment of children with BECTS. A prospective, open-label pilot trial prior to a controlled, randomised, double-blind German multicentre trial (HEAD-Study)

Schäfer, C.

Cerebral palsy covers Segawa syndrome

Schäfer, P.

Capillary microscopy and hemorheology in children during antiepileptic monotherapy with carbamazepine and valproate

Schaible, T.

Maturation of the autonomic nervous system: differences in heart rate variability in premature vs. term infants

Schallner, J.

Epilepsy and mental retardation with a distinctive facial phenotype – diagnosis on the spot with moleculargenetic confirmation – Mowat-Wilson syndrome

Schaper, J.

Congenital facial palsy and peripheral neuropathy. Manifestation of Neurofibromatosis Type 2 in childhood

Schara, U.

MuSK autoantibody positive myasthenia gravis in a 14 year old boy: difficulties in diagnosis and response to treatment with plasmapheresis and immunosuppression

Schäuble, B.

Fast titration of adjunctive topiramate in paediatric patients with difficult-to-treat epilepsy

Scheer, I.

Macrocephaly in a 10-week-old infant: isolated symptom of a citrobacter encephalitis with intracranial abscesses

Scheinemann, K.

Outcome of intraspinal tumours in children: long-term complications and quality of life

Scheithauer, S.

Diagnostic impact of intrathecally synthesized specific anti-viral antibodies

Schiffmann, H.

Acute cerebellitis with fatal and near-fatal course

Schlicke, M.

Comparison of the disease course of two patients with SMARD1

Schmidt, F.

Intracranial hypotension synodome – a rare cause of postural headache

Schmidt, J.

Proinflammatory molecules such as IFN-gamma and iNOS are not expressed in 25F9 positive macrophages in dermatomyositis

Schmidt, K.

Mydriasis without reaction to light, normal vigilance and pharyngitis: an unusual disorder

Schmitt, B.

Neonatal seizures: eyes open or closed?

Schmitt-Mechelke, T.

Chameleon Moebius syndrome

Sinus venous thrombosis in Swiss children

Schreiber, K.

Identification of a novel inborn neurodegenerative disease of childhood: cathepsin D deficiency

Schreiner, A.

Fast titration of adjunctive topiramate in paediatric patients with difficult-to-treat epilepsy

Schroeter, M.

Congenital facial palsy and peripheral neuropathy. Manifestation of Neurofibromatosis Type 2 in childhood

Mydriasis without reaction to light, normal vigilance and pharyngitis: an unusual disorder

Schröttner, O.

Stereotactic radiosurgery for hypothalamic hamartomas

Schulze, J.

Cranial metastasis of a 13-year-old patient with bronchial carcinoma

Schulze-Bonhage, A.

Usefulness of combined MEG and voxel-based morphometric MRI analysis in cryptogenic frontal lobe epilepsy

Schulz-Schaeffer, W.

Proinflammatory molecules such as IFN-gamma and iNOS are not expressed in 25F9 positive macrophages in dermatomyositis

Mitochondrial Myopathies in childhood and adolescence – Presentation, diagnosis und treatment

Schwarz, R.

Clinical spectrum of polymerase-gamma mutation in 9 children

Schwarzbraun, T.

Mental retardation in a girl with a subtelomeric 20q deletion and loss of the myelin transcription factor 1 (MYT1)

Seifert, T.

MuSK autoantibody positive myasthenia gravis in a 14 year old boy: difficulties in diagnosis and response to treatment with plasmapheresis and immunosuppression

Seitz, R.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Sewell, A.

A rare progressive neurometabolic disease (L-2-hydroxyglutaric aciduria) diagnosed by urinary organic acid analysis

Shazi, N.

Assessment of the autonomic nervous system function in infants: the pupillary light reflex: normative data and physiological observations

Siebert, S.

Usefulness of combined MEG and voxel-based morphometric MRI analysis in cryptogenic frontal lobe epilepsy

Siekmann, R.

Rapidly progressive moyamoya syndrome in a 19-month old girl with Bartonella henselae infection and Factor V Leiden mutation

Smitka, M.

Partially thrombosed megadolichobasilar artery in an 8-year old child with recurrent episodes of somnolence

Sojka, S.

Intracranial hypotension synodome – a rare cause of postural headache

Soliz, J.

Differential up-regulation of hypoxia-inducible vasoactive factors in fetal mouse brain in vivo upon intrauterine hypoxia

Specht, U.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Sperfeld, A. D.

Difficulties in diagnosing progressive bulbar paralysis (Fazio-Londe disease)

Sperl, W.

Clinical spectrum of polymerase-gamma mutation in 9 children

Sperner, J.

Cognition and behaviour in children and young adults related to monotherapy with valproic acid, carbamazepine and sulthiam – First results

FLIP&FLAP: Development and evaluation of a structured epilepsy education programme for children and adolescents with epilepsy and their parents

Sponholz, S.

Phenotype of children with congenital SEPN1-related myopathy and rigid spine

Sprinz, A.

Morbus Hallervorden-Spatz and atomoxetin: a therapeutic option?

Staudt, M.

Increased fMRI activation in the primary sensorimotor cortex (M1S1) after constraint induced movement therapy in congenital hemiparesis

Stein, S.

Validity of the Gross Motor Function Measure in children and adolescents with traumatic brain injury

Steiner, H. H.

Benefit of vagal nerve stimulation in epilepsia partialis continua: a case report

Steinfeld, R.

Identification of a novel inborn neurodegenerative disease of childhood: cathepsin D deficiency

Steinhoff, B. J.

Usefulness of combined MEG and voxel-based morphometric MRI analysis in cryptogenic frontal lobe epilepsy

Steinlin, M.

Sinus venous thrombosis in Swiss children

Stenger, R. D.

Indication and outcome of decompressive craniectomy of 6 children and teenagers with not conservative influenced posttraumatic cerebral swelling

Stettner, G. M.

Comparative studies on the respiratory dysfunction in Rett syndrome patients and the corresponding mouse model

Stoltenburg-Didinger, G.

Phenotype of children with congenital SEPN1-related myopathy and rigid spine

Strasser, K.

Differential up-regulation of hypoxia-inducible vasoactive factors in fetal mouse brain in vivo upon intrauterine hypoxia

Stülpnagel-Oefele, C.

Benign Idiopathic Focal Epileptiform Discharges of Childhood (BIFEDC) and Benign Idiopathic Focal Epilepsies of Childhood (BIFEC) in children with drug-ressistant symptomatic focal epilepsies

Surtees, R.

Paroxysmal eating-induced dystonic choreoathetosis – a second case

Tegtmayer, F.

Clinical spectrum of polymerase-gamma mutation in 9 children

Thyen, U.

FLIP&FLAP: Development and evaluation of a structured epilepsy education programme for children and adolescents with epilepsy and their parents

Tibussek, D.

Congenital facial palsy and peripheral neuropathy. Manifestation of Neurofibromatosis Type 2 in childhood

Benign infantile convulsions associated with mild gastroenteritis. Case report and review of the literature

Shuddering attacks as an important differential diagnosis of infantile epilepsy. A video-EEG presentation

Traus, M.

Cognition and behaviour in children and young adults related to monotherapy with valproic acid, carbamazepine and sulthiam – First results

Treiss, I.

Capillary microscopy and hemorheology in children during antiepileptic monotherapy with carbamazepine and valproate

Cognition and behaviour in children and young adults related to monotherapy with valproic acid, carbamazepine and sulthiam – First results

Trollmann, R.

Differential up-regulation of hypoxia-inducible vasoactive factors in fetal mouse brain in vivo upon intrauterine hypoxia

Tscharre, A.

Clinical spectrum of polymerase-gamma mutation in 9 children

Tschernatsch, M.

Surface-binding autoantibodies in childhood opsoclonus-myoclonus syndrome – binding and pathogenic effects of autoantibodies

Tuxhorn, I. E. B.

Vagusnerve stimulation in paediatric epilepsy: Bethel experience 2000–2004

Good seizure outcome after epilepsy surgery in young children with tuberous sclerosis complex

Usefulness of combined MEG and voxel-based morphometric MRI analysis in cryptogenic frontal lobe epilepsy

Developmental progress in paediatric temporal lobe epilepsy

Tzitiridou, M.

Benign paroxysmal vertigo and migraine in children: epidemiological evidence

Prognostic markers for multiple febrile seizure recurrences

Uhlenberg, B.

Macrocephaly in a 10-week-old infant: isolated symptom of a citrobacter encephalitis with intracranial abscesses

Unger, F.

Stereotactic radiosurgery for hypothalamic hamartomas

Utzig, N.

Severe mitochondrial disorder in spite of normal findings? Alpers syndrome due to homozygosity for A467T mutation in POLG gene

van der Knaap, M. S.

Progressive ataxia and symptomatic epilepsy in a case of leukoencephalopathy with brainstem and spinal cord involvement

Atypical variant of Alexander's disease with involvement of the spinal cord

Vincent, A.

MuSK autoantibody positive myasthenia gravis in a 14 year old boy: difficulties in diagnosis and response to treatment with plasmapheresis and immunosuppression

Vlaho, S.

Fatal course of maple syrup urine disease (MSUD) encephalopathy in a 6 year old boy with characteristic MRI-changes

Successful anticonvulsive therapy with D/L 3-hydroxybutyrate and ketogenic diet in a boy with agininosccinate lyase deficiency and status epileptics minor

A rare progressive neurometabolic disease (L-2-hydroxyglutaric aciduria) diagnosed by urinary organic acid analysis

Complex intracerebral malformation with large occipital encephalocele – diagnose and interdisciplinary management

Difficulties in diagnosing progressive bulbar paralysis (Fazio-Londe disease)

Normal ventricular size in brain imaging does not exclude blockage of cerebrospinal fluid shunts

Cranial metastasis of a 13-year-old patient with bronchial carcinoma

Effect of intrathecal methotrexate on biogenic amines in CSF of children and adolescents with acute lymphoblastic leukaemia enrolled in the ALL-BFM 2000 multicentre treatment study

Voit, T.

Biliary atresia as initial manifestation of Niemann Pick C1 disease

Vollmer, B.

Development of preterm children with early postnatally-acquired cytomegalovirus infection via breast milk

von Au, K.

Comparison of the disease course of two patients with SMARD1

von Buch, C.

Autonomic function in children and adolescents with neurogenic syncopes

von der Hagen, M.

Progressive ataxia and symptomatic epilepsy in a case of leukoencephalopathy with brainstem and spinal cord involvement

Progressive leucoencephalopathy with macrocephaly, optic atrophy, epileptic seizures, and primary ovarian dysfunction with relative preservation of cognitive functions

Partially thrombosed megadolichobasilar artery in an 8-year old child with recurrent episodes of somnolence

Phenotype of children with congenital SEPN1-related myopathy and rigid spine

Vry, J.

Validity of the Gross Motor Function Measure in children and adolescents with traumatic brain injury

Wagner, M.

Congenital myopathy with rigid spine caused by Selenoproteine 1- deficiency

Wagner, S.

Cognition and behaviour in children and young adults related to monotherapy with valproic acid, carbamazepine and sulthiam – First results

Walther, M.

Increased fMRI activation in the primary sensorimotor cortex (M1S1) after constraint induced movement therapy in congenital hemiparesis

Validity of the Gross Motor Function Measure in children and adolescents with traumatic brain injury

Weber, A.

Acute chorea as leading symptom in systemic lupus erythomatosus

Weber, P.

Intrathecal Baclofen therapy in children and young adults: first experience

Weber, Y. G.

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Weglage, J.

Morbus Hallervorden-Spatz and atomoxetin: a therapeutic option?

Weidner, B.

Valproic acid induced pancreatitis: 16 new cases and literature overview

Valproic acid induced hepatopathy – Nine new fatalities in Germany from 1994–2003

Weis, R.

L-Dopa/Carbidopa-therapy in children

Cerebral palsy covers Segawa syndrome

Weiss, S.

Sleep-related central respiratory drive disorder in so far unidentified primary disease

Weissenmayer, H.

Validity of the Gross Motor Function Measure in children and adolescents with traumatic brain injury

Weissert, M.

Brainstem auditory evoked potentials in the diagnosis of congenital hearing impairment

Sinus venous thrombosis in Swiss children

Wenzel, D.

Differential up-regulation of hypoxia-inducible vasoactive factors in fetal mouse brain in vivo upon intrauterine hypoxia

Editorial

Wenzl, T. G.

Application of Cox regression analysis to identify perinatal risk factors for neurodevelopmental outcome

Wiemer-Kruel, A.

Valproic acid induced pancreatitis: 16 new cases and literature overview

Wiersbitzky, H.

Indication and outcome of decompressive craniectomy of 6 children and teenagers with not conservative influenced posttraumatic cerebral swelling

Wilichowski, E.

Proinflammatory molecules such as IFN-gamma and iNOS are not expressed in 25F9 positive macrophages in dermatomyositis

Mitochondrial Myopathies in childhood and adolescence – Presentation, diagnosis und treatment

Wilmsmeyer, M.

Smith-Lemli-Opitz syndrome: case report on two patients with different clinical presentation

Witsch, M.

Capillary microscopy and hemorheology in children during antiepileptic monotherapy with carbamazepine and valproate

Woermann, F.

Developmental progress in paediatric temporal lobe epilepsy

Wohlrab, G.

Neonatal seizures: eyes open or closed?

Wolf, N. I.

Successful therapy with glibenclamid in a patient with a muation of KIR 6.2 subunit of the ATP-sensitive potassium channel

Acute chorea as leading symptom in systemic lupus erythomatosus

Epilepsies in mitochondrial disorders: seizure types and history

Differential diagnosis of gelastic seizures beside hypothalamic hamartoma

Wolff, M.

Valproic acid induced pancreatitis: 16 new cases and literature overview

Wölfing, C.

Capillary microscopy and hemorheology in children during antiepileptic monotherapy with carbamazepine and valproate

Wolters, B.

Long-term out-come, epidemiology and seizure recurrence of children with epilepsy of the University of Leipzig

Yale, C.

Paroxysmal eating-induced dystonic choreoathetosis – a second case

Zehnder, D.

Outcome of intraspinal tumours in children: long-term complications and quality of life

Outcome of brain tumour in children less than 1 year of age: long-term complications and quality of life

Zentner, J.

Usefulness of combined MEG and voxel-based morphometric MRI analysis in cryptogenic frontal lobe epilepsy

Zielen, S.

Cranial metastasis of a 13-year-old patient with bronchial carcinoma

Zobel, G.

MuSK autoantibody positive myasthenia gravis in a 14 year old boy: difficulties in diagnosis and response to treatment with plasmapheresis and immunosuppression

Zuzak, T. J.

Outcome of brain tumour in children less than 1 year of age: long-term complications and quality of life

Zweier, C.

Epilepsy and mental retardation with a distinctive facial phenotype – diagnosis on the spot with moleculargenetic confirmation – Mowat-Wilson syndrome