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Abels, C.
Epilepsy in vitamin B12 deficiency and its treatment in infancy
Autosomal dominant chin myoclonus
Abicht, A.
mitoNET – German Network for mitochondrial disorders
Acham-Roschitz, B.
Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations
Achatz, E.
Homocystein as an important diagnostic marker of remethylation defects – A case report
Aebi, C.
Bannwarth's syndrome – A rare but important manifestation of neuroborreliosis in childhood
Ahtig, U.
Diagnostic strategy in mitochondrial disorders – An update
Ahting, U.
Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue
Aksu, F.
Quantitative Sensory Testing (QST) in children and adolescents
Alber, M.
Neurocysticercosis in a 10 year-old boy in Germany
Polyneuropathy and hepatopathy as an infantile manifestation of a POLG1 gene defect
Albrecht, U.
Cardiac arrest in a patient with glutaric aciduria type II
Alesch, F.
Deep-brain stimulation in a boy with DYT1 dystonia
Allkemper, T.
Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?
Arend, M.
Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)
Arning, L.
Ataxia with oculomotor apraxia 1 (AOA1) in a consanguineous Pakistanian familiy
Atypical clinical presentation of a girl with episodic ataxia type II
Ausserer, B.
Posterior reversible encephalopathy syndrome (PRES)
Bajer-Kornek, B.
Epidemiology of pediatric multiple sclerosis in Austria
Baldeweg, T.
Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI
Balmer, C.
Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development
Bast, T.
Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient
Baudhuin, J. A.
Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®
Baumann, M.
Uncommon manifestations of childhood neuroborreliosis
Baumgartner, M.
Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development
Baumhackl, U.
Epidemiology of pediatric multiple sclerosis in Austria
Becher, T.
Sandifers syndrome – Unusual case report and review of the literature
Dystonic movements and developmental coordination disorder – Successful treatment with methylphenidate
Beck, M.
GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase
Becker, M.
Modified memory processes in children with febrile seizures: Analysis of event-related potentials
Beckhaus, M.
A series of 34 patients with Rasmussen's encephalitis: Clinical course, EEG- and MRI findings
Benninger, F.
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Ben-Omran, T.
GLUT1 deficiency syndrome in a consanguineous Arab family carrying a novel homozygous missense mutation
Bernhard, M. K.
Seizures caused by accidental dimenhydriante intoxication
Toxic effects of lamotrigine ingestion in children
Miller Fisher syndrome and Guillain Barré syndrome with ophtamloplegia: Two cases with overlapping phenotype
Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig
Chronic fatigue and pain syndrome caused by persistent intoxication with cactus spurge in a 12-year-old girl
Bertsche, A.
Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient
GLUT1 deficiency in a child with a movement disorder
Berweck, S.
Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases
Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up
Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level
Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy
Robotic-assisted treadmill therapy enhances motor functions in children with bilateral spastic cerebral palsy
Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia
Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia
Bevot, A.
Polyneuropathy and hepatopathy as an infantile manifestation of a POLG1 gene defect
Bien, C. G.
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder
Bigi, S.
Bannwarth's syndrome – A rare but important manifestation of neuroborreliosis in childhood
Therapy of sinus venous thrombosis in childhood – A standardised treatment protocol – Call for participation
Birnbacher, R.
Uncommon manifestations of childhood neuroborreliosis
Biste, M.
Improved molecular diagnostics for patients with respiratory chain complex deficiency
Bittner, R.
Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations
Blankenburg, M.
Quantitative Sensory Testing (QST) in children and adolescents
Blaschek, A.
Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)
Boekens, H.
Quantitative Sensory Testing (QST) in children and adolescents
Böhmer, S.
Copper histidine therapy started in a boy at the age of three years – Treatment option for a mild form of Menkes's disease
Boltshauser, E.
Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Pontine tegmental cap dysplasia: Two additional cases
Boor, R.
Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
Boppel, T.
Deep brain stimulation in children and adolescents with dystonia
Borggraefe, I.
Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level
Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy
Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia
Borggräfe, I.
Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases
Robotic-assisted treadmill therapy enhances motor functions in children with bilateral spastic cerebral palsy
Bötzel, K.
Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia
Braulke, T.
Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship
Breuer, K.
Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia
Brocke, K. S.
Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report
Brockmann, K.
Ophthalmoplegic migraine (OM) with early-onset recurrent oculomotor palsy of the left eye in a 6-year-old boy
Brück, W.
Natalizumab in 4 cases of pediatric multiple sclerosis
Brunner-Krainz, M.
20 years evaluation of pediatric patients with encephalitis in the PICU
Febrile seizures – First symptom of Rasmussenencephalitis
Homocystein as an important diagnostic marker of remethylation defects – A case report
Burdach, S.
Hennekam-syndrome with unusual MRI-changes and symptomatic epilepsy
Burfeind, P.
CDKL5 mutation in neonatal onset of epilepsy
Calaminus, G.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Christen, H. J.
Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation
Cowley, M. A.
Peripheral alpha MSH in childhood obesity and craniopharyngioma
Cross, J. H.
Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI
Czech, T.
Surgery during early life in children with intractable epilepsy – A prospective evaluation
Danek, A.
Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia
Das, A.
Treatment of NPC with miglustat in Germany
Manifestation and diagnosis of NPC disease in Germany
Das, A. M.
Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure
M. Scheie: Failure of enzyme replacement therapy to prevent CNS- and spinal-lesions
Datta, A. N.
Acute disseminated encephalomyelitis review in 8 pediatric patients
Daumer-Haas, C.
Accessory nipple as key symptom in diagnosis of Mowat-Wilson syndrome
Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia
Davids, S.
Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity
Degos, V.
Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease
De Haan, B.
Early determination of somatosensory cortex
Della Marina, A.
Ataxia with oculomotor apraxia 1 (AOA1) in a consanguineous Pakistanian familiy
Delvendahl, I.
Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?
Denecke, J.
A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity
Dercks, M.
Focal dystonia of dominant hand in a 13 year old girl: Action dystonia successfully treated by botulinumtoxine A (Xeomin®)
Treatment of cerebral palsy: Use of botulinum neurotoxin type A free of complexing proteins (Xeomin®) in childhood
Deuschle, K.
CDKL5 mutation in neonatal onset of epilepsy
Dickhaus, H.
Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)
Domin, M.
Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity
Donnerstag, F.
M. Scheie: Failure of enzyme replacement therapy to prevent CNS- and spinal-lesions
Drack, F.
Outcome of acute peripheral facial palsy in children – A catamnestic study of 84 patients
Drechsel-Baeuerle, U.
VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data
Dreiwes, C.
Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®
Dressler, A.
Surgery during early life in children with intractable epilepsy – A prospective evaluation
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Drosten, C.
Neonatal encephalitis through human parechoviruses with signs of extensive white matter injury – Case study and comparison to existing published cases
du Plessis, A. J.
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Dütting, T.
Neonatal encephalitis through human parechoviruses with signs of extensive white matter injury – Case study and comparison to existing published cases
Ebinger, F.
Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient
Acute motor and sensory axonal neuropathy (AMSAN) in a 7-year-old boy. A cases report
Deep brain stimulation in children and adolescents with dystonia
Treatment of NPC with miglustat in Germany
GLUT1 deficiency in a child with a movement disorder
Atypical clinical presentation of a girl with episodic ataxia type II
Manifestation and diagnosis of NPC disease in Germany
Eder, H. G.
Febrile seizures – First symptom of Rasmussenencephalitis
Ehrich, J. H. H.
Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure
Eichholz, S.
Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)
Einspieler, C.
Assessment of spontaneous movements in an infant with Peters anomaly
Is there an association between Touwen's neurological examination and the Zuerich neuromotor assessment?
Associated movements in 5- to 10-year-old infants
A possible association between genotypes and early signs of Rett disorder
The Preserved Speech Variant of Rett syndrome: Specificity of atypicality?
Elpers, C.
Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?
Emser, A.
Low grade glioma in pediatric NF-1 patients
Enrion, P. J.
Peripheral alpha MSH in childhood obesity and craniopharyngioma
Ertl-Wagner, B.
Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia
Erwa, W.
Homocystein as an important diagnostic marker of remethylation defects – A case report
Esser, N.
CDKL5 mutation in neonatal onset of epilepsy
Fahrig, A.
Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report
Faldum, A.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients
Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Fantur, K.
Imino analogues of galactose: Inhibitors of human acid β-D-Galactosidase and putative pharmacological chaperones for the treatment of GM1-Gangliosidosis
GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase
Feichtinger, M.
Febrile seizures – First symptom of Rasmussenencephalitis
Feucht, M.
Surgery during early life in children with intractable epilepsy – A prospective evaluation
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Do children with drug resistant epilepsy and low IQ also improve after epilepsy Ssrgery?
Fiedler, B.
Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?
Autosomal dominant chin myoclonus
A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity
Fiedler, B. J.
Epilepsy in vitamin B12 deficiency and its treatment in infancy
Fleischhack, G.
Severe generalized neuropathy in an 18-year-old patient with hereditary sensory-motor polyneurpathy (HMSN) type 1 treated with vincristine due to acute leukemia
Forstner, R.
Pontine tegmental cap dysplasia: Two additional cases
Fowler, B.
Homocystein as an important diagnostic marker of remethylation defects – A case report
Franke, A.
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
Freidl, T.
Opsoklonus-Myoklonus-Syndrom
Freilinger, M.
Surgery during early life in children with intractable epilepsy – A prospective evaluation
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Deep-brain stimulation in a boy with DYT1 dystonia
Freisinger, P.
Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue
Diagnostic strategy in mitochondrial disorders – An update
mitoNET – German Network for mitochondrial disorders
Improved molecular diagnostics for patients with respiratory chain complex deficiency
Frey, S. G.
Acute disseminated encephalomyelitis review in 8 pediatric patients
Fritsch, M. J.
Outcome of endoscopic therapy of complex hydrocephalus
Fuchs, T.
Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia
Ganslandt, O.
Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report
Gärtner, J.
Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency
Ophthalmoplegic migraine (OM) with early-onset recurrent oculomotor palsy of the left eye in a 6-year-old boy
The structure of tripeptidyl peptidase I (TPP1) provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis
Cerebral MRI as a valuable tool for the diagnosis of Zellweger syndrome spectrum patients and patients with peroxisomal β-oxidation defects
Natalizumab in 4 cases of pediatric multiple sclerosis
Cyclic Esotropia – A rare differenzial diagnosis in non paralytic strabismus in childhood
Gebhardt, U.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Peripheral alpha MSH in childhood obesity and craniopharyngioma
Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients
Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Gehrmann, A.
Intracerebral calcification in a newborn – Not always a connatal infection
Geis, T.
Tumor induced Hemichorea
Gerecke, A.
Wernicke encephalopathy in childhood
Gerstner, K.
Modified memory processes in children with febrile seizures: Analysis of event-related potentials
Gnekow, A.
Low grade glioma in pediatric NF-1 patients
Gontard, A. von
Modified memory processes in children with febrile seizures: Analysis of event-related potentials
Gortner, L.
Modified memory processes in children with febrile seizures: Analysis of event-related potentials
The prognostic value of EEG in children with minor head trauma
Gotwald, T.
Cardiac arrest in a patient with glutaric aciduria type II
Gouadon, E.
Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease
Gratzki, N.
Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report
Greiner, J.
Acute basilar artery thrombosis in childhood: A therapeutic dilemma
Grenzebach, U.
Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?
Gressens, P.
Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease
Grodd, W.
Diagnostic value of magnetic resonance imaging and morphometry of the corpus callosum in children with isolated mental retardation
A new score for assessing white matter changes in metachromatic leukodystrophy
Gronborg, S.
Cerebral MRI as a valuable tool for the diagnosis of Zellweger syndrome spectrum patients and patients with peroxisomal β-oxidation defects
Gröppel, G.
Surgery during early life in children with intractable epilepsy – A prospective evaluation
Gross, C. D.
Mutation analysis of the SCN1A gene for suspected Dravet syndrome/GEFS+ – High detection yield, unsatisfactory prognostic value
Gruber-Sedlmayr, U.
20 years evaluation of pediatric patients with encephalitis in the PICU
Plasmapheresis in the treatment of pediatric patients with neurological diseases: 10 years experience
Opsoklonus-Myoklonus-Syndrom
Grüne, T.
The structure of tripeptidyl peptidase I (TPP1) provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis
Grønborg, S.
Ophthalmoplegic migraine (OM) with early-onset recurrent oculomotor palsy of the left eye in a 6-year-old boy
Gudegast, C.
Outcome of endoscopic therapy of complex hydrocephalus
Haase, C.
Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease
Haas-Lude, K.
Neurocysticercosis in a 10 year-old boy in Germany
Haberlandt, E.
Proinflamatory cytokines in children with febrile seizures
Cardiac arrest in a patient with glutaric aciduria type II
Habermehl, P.
Case report: Rapid evolving, severe encephalopathy, caused by nutritive cobalamin deficiency due to subclinical maternal pernicious anemia
Long-term antikoagulation in a neonate with sinovenous thrombosis and stroke. Case presentation and review of the literature
Hackmann, K.
Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report
Hackstein, H.
IAHSP caused by maternal uniparental isodisomy in ALS2
Hadders-Algra, M.
Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)
Hagen, M. von der
Postinfectious autoimmune-mediated encephalitis versus relapse of herpes encephalitis?
Muscular magnet resonance imaging (M-MRI) in α-Dystroglykanopathies – clinical course of two juvenile patients with LGMD2I and LGMD2M
A rare Ca2+ channel mutation R528G identified in a patient with autosomal dominant hypokalemic periodic paralysis (HypoPP-1)
Hahn, A.
Non-invasive tension-time-index and ventilator use in Duchenne muscular dystrophy
Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease
Hahn, G.
Postinfectious autoimmune-mediated encephalitis versus relapse of herpes encephalitis?
Pontine tegmental cap dysplasia: Two additional cases
Muscular magnet resonance imaging (M-MRI) in α-Dystroglykanopathies – clinical course of two juvenile patients with LGMD2I and LGMD2M
Hahn, J.
Continous intrathecal baclofen (cITB) therapy terminates spinal spasms mimicking tonic seizures in a teenager with severe spastic cerebral palsy with total body involvement and cervical dystonia
Hainfellner, J.
Surgery during early life in children with intractable epilepsy – A prospective evaluation
Hamm, A.
Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity
Hampel, O.
Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study
Hanganu, I.
KCNQ potassium channels are critical determinants of neuronal network activity in neonatal mouse brain
Hartig, M. B.
Clinical characterisation of NBIA patients with and without mutation in PANK2 gene
Hartmann, H.
Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure
M. Scheie: Failure of enzyme replacement therapy to prevent CNS- and spinal-lesions
Hartmann, M.
Oxcarbazepine accelerates steroid elimination in young men with epilepsy due to cytochrome P450 3A4 induction
Hartung, R.
Treatment of NPC with miglustat in Germany
Manifestation and diagnosis of NPC disease in Germany
Harzer, K.
Manifestation and diagnosis of NPC disease in Germany
Hasmann, R.
Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study
Hasmann, S.
Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study
Haug, V.
Severe confusion and agitation as predominant symptom of a hemiplegic migraine with mutation in ATP1A2
Hauschke, D.
Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?
Hauser, E.
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Hawellek, N.
Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure
Hechler, T.
Quantitative Sensory Testing (QST) in children and adolescents
Hecker, A.
Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease
Heinen, F.
Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases
Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up
Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level
Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy
Robotic-assisted treadmill therapy enhances motor functions in children with bilateral spastic cerebral palsy
Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia
Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia
Helbig, I.
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data
Hempel, M.
Hennekam-syndrome with unusual MRI-changes and symptomatic epilepsy
Clinical characterisation of NBIA patients with and without mutation in PANK2 gene
Herbertz, S.
Fast recovery after 5 months in persistent vegetative state
Hernáiz Driever, P.
Low grade glioma in pediatric NF-1 patients
Herzfeld, T.
IAHSP caused by maternal uniparental isodisomy in ALS2
Himpel, M.
Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig
Hirschburger, M.
Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease
Hirschfeld, H.
Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity
Hofer, D.
Imino analogues of galactose: Inhibitors of human acid β-D-Galactosidase and putative pharmacological chaperones for the treatment of GM1-Gangliosidosis
GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase
Hoffmann, G. F.
Multiple epiphyseal dysplasia as differenzial diagnosis in patients with L-Dopa responsive dystonia
Hoffmann, L.
Combination of early endotracheal Surfactant and nasal continous positive airwaypressure (CPAP): 15–32-month outcome of extremly low birth weight preterm infants (ELBW)
Högler, W.
Oxcarbazepine accelerates steroid elimination in young men with epilepsy due to cytochrome P450 3A4 induction
Holl, R.
Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study
Holthausen, H.
Hemiplegic migraine with cerebellar atrophy: A second pediatric case
Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)
Hornstein, S.
Low grade glioma in pediatric NF-1 patients
Horvarth, R.
Improved molecular diagnostics for patients with respiratory chain complex deficiency
Horvath, R.
Polyneuropathy and hepatopathy as an infantile manifestation of a POLG1 gene defect
Hoy, L.
Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure
Huisman, T. A.
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Huppke, B.
Natalizumab in 4 cases of pediatric multiple sclerosis
Huppke, P.
Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency
Ophthalmoplegic migraine (OM) with early-onset recurrent oculomotor palsy of the left eye in a 6-year-old boy
Natalizumab in 4 cases of pediatric multiple sclerosis
Huß, K.
Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases
Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level
Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy
Ihorst, G.
Treatment of Duchenne muscular dystrophy with cyclosporin A – A randomized, double-blind, placebo controlled trial
Ikonomidou, C.
Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission
Muscular magnet resonance imaging (M-MRI) in α-Dystroglykanopathies – clinical course of two juvenile patients with LGMD2I and LGMD2M
Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report
Ikonomidou, H.
Postinfectious autoimmune-mediated encephalitis versus relapse of herpes encephalitis?
Illerhaus, M.
Focal dystonia of dominant hand in a 13 year old girl: Action dystonia successfully treated by botulinumtoxine A (Xeomin®)
Illsinger, S.
Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure
M. Scheie: Failure of enzyme replacement therapy to prevent CNS- and spinal-lesions
Isbrandt, D.
KCNQ potassium channels are critical determinants of neuronal network activity in neonatal mouse brain
Jagdhuhn, M.
Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity
Jäger, G.
Citrobacter koseri meningitis – A rare and severe disease in the neonate. A case report
Johann to Settel, E.
Severe generalized neuropathy in an 18-year-old patient with hereditary sensory-motor polyneurpathy (HMSN) type 1 treated with vincristine due to acute leukemia
Jopp-Petzinna, G.
Combination of early endotracheal Surfactant and nasal continous positive airwaypressure (CPAP): 15–32-month outcome of extremly low birth weight preterm infants (ELBW)
Juenemann, S.
Acute basilar artery thrombosis in childhood: A therapeutic dilemma
Juenger, H.
Early determination of somatosensory cortex
Jung, N. H.
Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up
Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?
Jurkat-Rott, K.
A rare Ca2+ channel mutation R528G identified in a patient with autosomal dominant hypokalemic periodic paralysis (HypoPP-1)
Kabus, M.
Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)
Kaindl, A. M.
Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission
Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease
Neuropathologic findings in patients with primary autosomal recessive microcephaly
Karall, D.
Proinflamatory cytokines in children with febrile seizures
Cardiac arrest in a patient with glutaric aciduria type II
Karch, D.
Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)
Karnath, H. O.
Early determination of somatosensory cortex
Kasahara, M.
GLUT1 deficiency syndrome – A novel phenotype and a novel mutation
Kattner, E.
Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation
Kehrer, C.
Clinical course of two siblings with Metachromatic Leukodystrophy (MLD) with and without Stem cell transplantation (SCT)
A new score for assessing white matter changes in metachromatic leukodystrophy
Kehrer, M.
The development of cerebral perfusion during the first three years of life: Long-term follow-up study of cerebral blood flow volume measurement in two healthy children
Keller-Stanislawski, B.
VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data
Kerr, A. M.
A possible association between genotypes and early signs of Rett disorder
Keyvani, K.
A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity
Kiening, K.
Deep brain stimulation in children and adolescents with dystonia
Kim, K. S.
Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report
Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)
Kim, S.
Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation
Kipp, K. H.
Modified memory processes in children with febrile seizures: Analysis of event-related potentials
Kirmess, B.
Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia
Kirschner, J.
Treatment of Duchenne muscular dystrophy with cyclosporin A – A randomized, double-blind, placebo controlled trial
Severe confusion and agitation as predominant symptom of a hemiplegic migraine with mutation in ATP1A2
Klaiber, M.
Robotic-assisted treadmill therapy enhances motor functions in children with bilateral spastic cerebral palsy
Klein, A.
Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development
Klepper, J.
Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency
GLUT1 deficiency syndrome – A novel phenotype and a novel mutation
GLUT1 deficiency syndrome in a consanguineous Arab family carrying a novel homozygous missense mutation
Klopstock, T.
mitoNET – German Network for mitochondrial disorders
Klose, J.
Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission
Kloss, M.
Deep brain stimulation in children and adolescents with dystonia
Kluger, G.
Provocation of seizures by vaccination with children suffering from SCN1A-mutation
Fast recovery after 5 months in persistent vegetative state
Patients with Dravet's syndrome and SCN1A-mutation with a benign course of illness – A case report with 6 patients
Kmiec, T.
Clinical characterisation of NBIA patients with and without mutation in PANK2 gene
Knecht, B.
Acute basilar artery thrombosis in childhood: A therapeutic dilemma
Knuf, M.
Case report: Rapid evolving, severe encephalopathy, caused by nutritive cobalamin deficiency due to subclinical maternal pernicious anemia
Long-term antikoagulation in a neonate with sinovenous thrombosis and stroke. Case presentation and review of the literature
Koch, J.
Uncommon manifestations of childhood neuroborreliosis
Treatment of West syndrome (WS) according to UKISS (United Kindom Infantile Spasms Study): A single centers experience
Pontine tegmental cap dysplasia: Two additional cases
Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue
Koch, S.
Treatment of NPC with miglustat in Germany
Manifestation and diagnosis of NPC disease in Germany
Kohlschmidt, N.
Mutation analysis of the SCN1A gene for suspected Dravet syndrome/GEFS+ – High detection yield, unsatisfactory prognostic value
Kohlschütter, A.
Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship
Kolb, R.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients
Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Kolzter, K.
Patients with Dravet's syndrome and SCN1A-mutation with a benign course of illness – A case report with 6 patients
König, S.
Partial response to the vagus nerve stimulation in twins with double cortex syndrome
Korall, H.
Screening for pyridoxine dependent epilepsy (PDE) by Tandem Mass Spectrometry (HPLC-MS/MS)
Korenke, C.
Treatment of NPC with miglustat in Germany
Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)
Manifestation and diagnosis of NPC disease in Germany
Korinthenberg, R.
Treatment of Duchenne muscular dystrophy with cyclosporin A – A randomized, double-blind, placebo controlled trial
Severe confusion and agitation as predominant symptom of a hemiplegic migraine with mutation in ATP1A2
Wernicke encephalopathy in childhood
Kornak, U.
Intractable seizures in malignant infantile osteopetrosis due to CLCN7 mutation: lysosomal aspects
Körte, I.
Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia
Kortmann, R.
Low grade glioma in pediatric NF-1 patients
Kortmann, R. D.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Kotzaeridou, U.
Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Acute motor and sensory axonal neuropathy (AMSAN) in a 7-year-old boy. A cases report
Atypical clinical presentation of a girl with episodic ataxia type II
Kotzot, D.
Cardiac arrest in a patient with glutaric aciduria type II
Krägeloh-Mann, I.
Clinical course of two siblings with Metachromatic Leukodystrophy (MLD) with and without Stem cell transplantation (SCT)
Neurocysticercosis in a 10 year-old boy in Germany
Diagnostic value of magnetic resonance imaging and morphometry of the corpus callosum in children with isolated mental retardation
A new score for assessing white matter changes in metachromatic leukodystrophy
Early determination of somatosensory cortex
Polyneuropathy and hepatopathy as an infantile manifestation of a POLG1 gene defect
Krätzner, R.
The structure of tripeptidyl peptidase I (TPP1) provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis
Kraus, C.
Accessory nipple as key symptom in diagnosis of Mowat-Wilson syndrome
Krause, M.
Deep brain stimulation in children and adolescents with dystonia
Kress, W.
A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity
Kreuder, J.
Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)
Kribs, A.
Combination of early endotracheal Surfactant and nasal continous positive airwaypressure (CPAP): 15–32-month outcome of extremly low birth weight preterm infants (ELBW)
Krick, C.
Modified memory processes in children with febrile seizures: Analysis of event-related potentials
Krischke, G.
Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)
Kruse, B.
Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship
Kuczaty, S.
Mutation analysis of the SCN1A gene for suspected Dravet syndrome/GEFS+ – High detection yield, unsatisfactory prognostic value
Kudernatsch, M.
Fast recovery after 5 months in persistent vegetative state
Kuhnke, N.
Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?
Kunz, W.
Mutation analysis of the SCN1A gene for suspected Dravet syndrome/GEFS+ – High detection yield, unsatisfactory prognostic value
mitoNET – German Network for mitochondrial disorders
Kurlemann, G.
Epilepsy in vitamin B12 deficiency and its treatment in infancy
Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?
Autosomal dominant chin myoclonus
A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity
Kyttällä, A.
Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship
Laccone, F.
The Preserved Speech Variant of Rett syndrome: Specificity of atypicality?
Lackner, H.
Opsoklonus-Myoklonus-Syndrom
Landgraf, M.
Toxic effects of lamotrigine ingestion in children
Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig
Chronic fatigue and pain syndrome caused by persistent intoxication with cactus spurge in a 12-year-old girl
Lauffer, H.
Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity
Le, Q.
KCNQ potassium channels are critical determinants of neuronal network activity in neonatal mouse brain
Lebrun, A. H.
Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship
Ledvinova, J.
GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase
Lehmann-Horn, F.
A rare Ca2+ channel mutation R528G identified in a patient with autosomal dominant hypokalemic periodic paralysis (HypoPP-1)
Lehner, K.
Fast recovery after 5 months in persistent vegetative state
Leiz, S.
Accessory nipple as key symptom in diagnosis of Mowat-Wilson syndrome
Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia
Lerche, H.
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
Lettau, M.
Neurocysticercosis in a 10 year-old boy in Germany
Limperopoulos, C.
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Lindbichler, F.
Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations
Lindhout, D.
VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data
Logeswaran, T.
Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)
Lombet, A.
Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease
Lorenz, I.
Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report
Lorenz, N.
Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)
Loron, G.
Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease
Lotte, J.
Provocation of seizures by vaccination with children suffering from SCN1A-mutation
Patients with Dravet's syndrome and SCN1A-mutation with a benign course of illness – A case report with 6 patients
Lotze, M.
Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity
Lücke, T.
Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure
M. Scheie: Failure of enzyme replacement therapy to prevent CNS- and spinal-lesions
Ludwig, H. C.
Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency
Luef, G.
Oxcarbazepine accelerates steroid elimination in young men with epilepsy due to cytochrome P450 3A4 induction
Lütjen, S.
Hemiplegic migraine with cerebellar atrophy: A second pediatric case
Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)
Mache, C. J.
Plasmapheresis in the treatment of pediatric patients with neurological diseases: 10 years experience
Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations
Madignier, F.
Improved molecular diagnostics for patients with respiratory chain complex deficiency
Maier, C.
Quantitative Sensory Testing (QST) in children and adolescents
Maier, O.
Citrobacter koseri meningitis – A rare and severe disease in the neonate. A case report
Makowski, C.
Hennekam-syndrome with unusual MRI-changes and symptomatic epilepsy
Mall, V.
Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases
Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up
Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?
Mantz, J.
Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease
Marquardt, T.
Treatment of NPC with miglustat in Germany
Manifestation and diagnosis of NPC disease in Germany
Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease
Marschik, P. B.
Is there an association between Touwen's neurological examination and the Zuerich neuromotor assessment?
Associated movements in 5- to 10-year-old infants
A possible association between genotypes and early signs of Rett disorder
The Preserved Speech Variant of Rett syndrome: Specificity of atypicality?
Marschitz, I.
20 years evaluation of pediatric patients with encephalitis in the PICU
Plasmapheresis in the treatment of pediatric patients with neurological diseases: 10 years experience
Martelli, M.
Neuropathologic findings in patients with primary autosomal recessive microcephaly
Mayer, H.
Surgery during early life in children with intractable epilepsy – A prospective evaluation
Mayr, H.
Diagnostic strategy in mitochondrial disorders – An update
Mayr, J.
Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue
Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations
Improved molecular diagnostics for patients with respiratory chain complex deficiency
Mayrhofer, H.
Diagnostic value of magnetic resonance imaging and morphometry of the corpus callosum in children with isolated mental retardation
Mecklinger, A.
Modified memory processes in children with febrile seizures: Analysis of event-related potentials
Mehrkens, J. H.
Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia
Meitinger, T.
mitoNET – German Network for mitochondrial disorders
Improved molecular diagnostics for patients with respiratory chain complex deficiency
Clinical characterisation of NBIA patients with and without mutation in PANK2 gene
Mengel, E.
Case report: Rapid evolving, severe encephalopathy, caused by nutritive cobalamin deficiency due to subclinical maternal pernicious anemia
Treatment of NPC with miglustat in Germany
Manifestation and diagnosis of NPC disease in Germany
Merkel, H. J.
Partial response to the vagus nerve stimulation in twins with double cortex syndrome
Merkenschlager, A.
Seizures caused by accidental dimenhydriante intoxication
Toxic effects of lamotrigine ingestion in children
Miller Fisher syndrome and Guillain Barré syndrome with ophtamloplegia: Two cases with overlapping phenotype
Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig
Chronic fatigue and pain syndrome caused by persistent intoxication with cactus spurge in a 12-year-old girl
Merten, A.
Diagnostic value of magnetic resonance imaging and morphometry of the corpus callosum in children with isolated mental retardation
Meyer, S.
Modified memory processes in children with febrile seizures: Analysis of event-related potentials
The prognostic value of EEG in children with minor head trauma
Meyer-Heim, A.
Robotic-assisted treadmill therapy enhances motor functions in children with bilateral spastic cerebral palsy
Michelakakis, H.
GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase
Miehe, U.
Seizures caused by accidental dimenhydriante intoxication
Moers, A. von
CDKL5 mutation in neonatal onset of epilepsy
Mole, S. E.
Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship
Möller-Hartmann, C.
Ataxia with oculomotor apraxia 1 (AOA1) in a consanguineous Pakistanian familiy
Moog, U.
Multiple epiphyseal dysplasia as differenzial diagnosis in patients with L-Dopa responsive dystonia
Morass, M.
Proinflamatory cytokines in children with febrile seizures
Morris-Rosendahl, D. J.
Muscular magnet resonance imaging (M-MRI) in α-Dystroglykanopathies – clinical course of two juvenile patients with LGMD2I and LGMD2M
Moser, A.
Opsoklonus-Myoklonus-Syndrom
Motz, R.
Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease
Muckenhaupt, T.
Neonatal encephalitis through human parechoviruses with signs of extensive white matter injury – Case study and comparison to existing published cases
Muhle, H.
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data
Müller, A.
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Müller, H. L.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Peripheral alpha MSH in childhood obesity and craniopharyngioma
Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients
Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Müller, I.
Clinical course of two siblings with Metachromatic Leukodystrophy (MLD) with and without Stem cell transplantation (SCT)
Müller, U.
IAHSP caused by maternal uniparental isodisomy in ALS2
Munk, I.
Partial response to the vagus nerve stimulation in twins with double cortex syndrome
Mütze, U.
Seizures caused by accidental dimenhydriante intoxication
Nagel, A.
Focal dystonia of dominant hand in a 13 year old girl: Action dystonia successfully treated by botulinumtoxine A (Xeomin®)
Multimodal treatment of Cerebral Palsy (CP) including physical therapy, Botulinumtoxin und Lokomat-Training: A case report
Treatment of cerebral palsy: Use of botulinum neurotoxin type A free of complexing proteins (Xeomin®) in childhood
Nagl, A.
Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)
Naxer, S.
Cyclic Esotropia – A rare differenzial diagnosis in non paralytic strabismus in childhood
Neu, A.
KCNQ potassium channels are critical determinants of neuronal network activity in neonatal mouse brain
Neubauer, B.
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
Non-invasive tension-time-index and ventilator use in Duchenne muscular dystrophy
Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease
Neuhann, T.
Pontine tegmental cap dysplasia: Two additional cases
Niederstadt, T.
Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?
Niesytto, C.
Outcome of endoscopic therapy of complex hydrocephalus
Nomayo, H. O.
IV Levetiracetam in the management of refractory complex-partial status epilepticus
Continous intrathecal baclofen (cITB) therapy terminates spinal spasms mimicking tonic seizures in a teenager with severe spastic cerebral palsy with total body involvement and cervical dystonia
Northam, G.
Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI
Oberle, A.
A possible association between genotypes and early signs of Rett disorder
The Preserved Speech Variant of Rett syndrome: Specificity of atypicality?
Obermaier-Kusser, B.
mitoNET – German Network for mitochondrial disorders
Obermeier, T.
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
Omran, H.
Severe confusion and agitation as predominant symptom of a hemiplegic migraine with mutation in ATP1A2
Opherk, K.
Clinical course of two siblings with Metachromatic Leukodystrophy (MLD) with and without Stem cell transplantation (SCT)
Opladen, T.
Multiple epiphyseal dysplasia as differenzial diagnosis in patients with L-Dopa responsive dystonia
Oster, I.
The prognostic value of EEG in children with minor head trauma
Pahs, G.
Surgery during early life in children with intractable epilepsy – A prospective evaluation
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI
Pal, A.
The structure of tripeptidyl peptidase I (TPP1) provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis
Pansy, J.
Assessment of spontaneous movements in an infant with Peters anomaly
Is there an association between Touwen's neurological examination and the Zuerich neuromotor assessment?
Associated movements in 5- to 10-year-old infants
Panzer, A.
CDKL5 mutation in neonatal onset of epilepsy
Pape, L.
Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure
Paschke, E.
Imino analogues of galactose: Inhibitors of human acid β-D-Galactosidase and putative pharmacological chaperones for the treatment of GM1-Gangliosidosis
Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation
GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase
Pauen, S.
Self regulation in preterms – preliminary data with regard to the assessment of „Effortful Control“
Paul, K.
Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation
GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase
Peineau, S.
Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease
Penzien, J.
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder
Pernice, W.
Miller Fisher syndrome and Guillain Barré syndrome with ophtamloplegia: Two cases with overlapping phenotype
Petermann, F.
Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study
Peters, J.
Accessory nipple as key symptom in diagnosis of Mowat-Wilson syndrome
Philippi, H.
Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)
Pietsch, T.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients
Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Low grade glioma in pediatric NF-1 patients
Pietz, J.
Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report
Acute motor and sensory axonal neuropathy (AMSAN) in a 7-year-old boy. A cases report
Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)
Self regulation in preterms – preliminary data with regard to the assessment of „Effortful Control“
Pilhatsch, A.
Febrile seizures – First symptom of Rasmussenencephalitis
Plecko, B.
Febrile seizures – First symptom of Rasmussenencephalitis
Abstracts of the 35th Annual Meeting of the Society of Neuropediatrics, „Gesellschaft für Neuropädiatrie“, 23rd to 26th April 2009
Plasmapheresis in the treatment of pediatric patients with neurological diseases: 10 years experience
Opsoklonus-Myoklonus-Syndrom
Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation
Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations
GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase
Homocystein as an important diagnostic marker of remethylation defects – A case report
Pohl, F.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Pohlmann-Eden, B.
A series of 34 patients with Rasmussen's encephalitis: Clinical course, EEG- and MRI findings
Poretti, A.
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Pontine tegmental cap dysplasia: Two additional cases
Porsche, B.
Surgery during early life in children with intractable epilepsy – A prospective evaluation
Do children with drug resistant epilepsy and low IQ also improve after epilepsy Ssrgery?
Prayer, D.
Surgery during early life in children with intractable epilepsy – A prospective evaluation
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Prechtl, H. F. R.
A possible association between genotypes and early signs of Rett disorder
Prokisch, H.
Diagnostic strategy in mitochondrial disorders – An update
mitoNET – German Network for mitochondrial disorders
Improved molecular diagnostics for patients with respiratory chain complex deficiency
Clinical characterisation of NBIA patients with and without mutation in PANK2 gene
Prokop, K.
Postinfectious autoimmune-mediated encephalitis versus relapse of herpes encephalitis?
Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report
Rankin, P.
Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI
Rapp, E. M.
Is there an association between Touwen's neurological examination and the Zuerich neuromotor assessment?
Rascher, W.
Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)
Rating, D.
GLUT1 deficiency in a child with a movement disorder
Rauchenzauner, M.
Oxcarbazepine accelerates steroid elimination in young men with epilepsy due to cytochrome P450 3A4 induction
Proinflamatory cytokines in children with febrile seizures
Rauscher, C.
Treatment of West syndrome (WS) according to UKISS (United Kindom Infantile Spasms Study): A single centers experience
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Pontine tegmental cap dysplasia: Two additional cases
Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue
GLUT1 deficiency syndrome – A novel phenotype and a novel mutation
Reinehr, T.
Peripheral alpha MSH in childhood obesity and craniopharyngioma
Reinhardt, K.
Cyclic Esotropia – A rare differenzial diagnosis in non paralytic strabismus in childhood
Reiser, M.
Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia
Reissig, A.
Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up
Reiter, E.
Surgery during early life in children with intractable epilepsy – A prospective evaluation
Reiter-Fink, E.
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Reith, W.
Modified memory processes in children with febrile seizures: Analysis of event-related potentials
Reithofer, E.
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Reuner, G.
Self regulation in preterms – preliminary data with regard to the assessment of „Effortful Control“
Reutlinger, C.
Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®
Rhein, M. von
Case report: Rapid evolving, severe encephalopathy, caused by nutritive cobalamin deficiency due to subclinical maternal pernicious anemia
Long-term antikoagulation in a neonate with sinovenous thrombosis and stroke. Case presentation and review of the literature
Richter, J. W.
Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation
Ring, E.
Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations
Rittinger, O.
Intractable seizures in malignant infantile osteopetrosis due to CLCN7 mutation: lysosomal aspects
Rödl, S.
20 years evaluation of pediatric patients with encephalitis in the PICU
Plasmapheresis in the treatment of pediatric patients with neurological diseases: 10 years experience
Rohrbach, M.
Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development
Rolinski, B.
Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue
Diagnostic strategy in mitochondrial disorders – An update
Improved molecular diagnostics for patients with respiratory chain complex deficiency
Roos, R.
Intracerebral calcification in a newborn – Not always a connatal infection
Rosewich, H.
Cerebral MRI as a valuable tool for the diagnosis of Zellweger syndrome spectrum patients and patients with peroxisomal β-oxidation defects
Rostasy, K.
Uncommon manifestations of childhood neuroborreliosis
Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)
Rostásy, K.
Proinflamatory cytokines in children with febrile seizures
Roth, C. L.
Peripheral alpha MSH in childhood obesity and craniopharyngioma
Roulet-Perez, E.
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Rutsch, F.
Treatment of NPC with miglustat in Germany
Manifestation and diagnosis of NPC disease in Germany
Sanchez-Albisua, I.
Diagnostic value of magnetic resonance imaging and morphometry of the corpus callosum in children with isolated mental retardation
Santer, R.
GLUT1 deficiency in a child with a movement disorder
Sassen, R.
Provocation of seizures by vaccination with children suffering from SCN1A-mutation
Mutation analysis of the SCN1A gene for suspected Dravet syndrome/GEFS+ – High detection yield, unsatisfactory prognostic value
Schaadt, A. K.
Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study
Schallner, J. C.
A rare Ca2+ channel mutation R528G identified in a patient with autosomal dominant hypokalemic periodic paralysis (HypoPP-1)
Schaper, J.
Copper histidine therapy started in a boy at the age of three years – Treatment option for a mild form of Menkes's disease
Schara, U.
Copper histidine therapy started in a boy at the age of three years – Treatment option for a mild form of Menkes's disease
Ataxia with oculomotor apraxia 1 (AOA1) in a consanguineous Pakistanian familiy
Scheer, I.
Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development
Scheffer, H.
GLUT1 deficiency syndrome – A novel phenotype and a novel mutation
GLUT1 deficiency syndrome in a consanguineous Arab family carrying a novel homozygous missense mutation
Scheffner, T.
Neonatal encephalitis through human parechoviruses with signs of extensive white matter injury – Case study and comparison to existing published cases
Schell-Apacik, C.
CDKL5 mutation in neonatal onset of epilepsy
Schenk, W.
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder
Schessl, J.
Treatment of Duchenne muscular dystrophy with cyclosporin A – A randomized, double-blind, placebo controlled trial
Schilling, S.
Tumor induced Hemichorea
Schimmel, M.
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder
Schitter, G.
Imino analogues of galactose: Inhibitors of human acid β-D-Galactosidase and putative pharmacological chaperones for the treatment of GM1-Gangliosidosis
Schittkowski, M.
Cyclic Esotropia – A rare differenzial diagnosis in non paralytic strabismus in childhood
Schlachter, K.
Posterior reversible encephalopathy syndrome (PRES)
Schlee-Böckh, K.
Long-term antikoagulation in a neonate with sinovenous thrombosis and stroke. Case presentation and review of the literature
Schlotawa, L.
Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency
Schmitt, C. P.
Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report
Schneider, C.
Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)
Scholl-Buergi, S.
Proinflamatory cytokines in children with febrile seizures
Scholl-Bürgi, S.
Cardiac arrest in a patient with glutaric aciduria type II
Schöls, L.
mitoNET – German Network for mitochondrial disorders
Schöning, M.
The development of cerebral perfusion during the first three years of life: Long-term follow-up study of cerebral blood flow volume measurement in two healthy children
Schramm, P.
Ophthalmoplegic migraine (OM) with early-onset recurrent oculomotor palsy of the left eye in a 6-year-old boy
Schranz, D.
Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)
Schreiber, S.
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
Schröder, A. S.
Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases
Schröder, H. W. S.
Outcome of endoscopic therapy of complex hydrocephalus
Schröder, S.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients
Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Schröder, S. A.
Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level
Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy
Schülke-Gerstenfeld, M.
mitoNET – German Network for mitochondrial disorders
Schulz, A.
Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship
Schulz, M.
Miller Fisher syndrome and Guillain Barré syndrome with ophtamloplegia: Two cases with overlapping phenotype
Schwartz, O.
Epilepsy in vitamin B12 deficiency and its treatment in infancy
Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?
Autosomal dominant chin myoclonus
A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity
Schweiger, B.
Copper histidine therapy started in a boy at the age of three years – Treatment option for a mild form of Menkes's disease
Schwinger, W.
Opsoklonus-Myoklonus-Syndrom
Seidl, R.
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Deep-brain stimulation in a boy with DYT1 dystonia
Seitz, A.
Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report
Sengupta, D.
Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient
Sergi, C.
Cardiac arrest in a patient with glutaric aciduria type II
Shamdeen, M. G.
Modified memory processes in children with febrile seizures: Analysis of event-related potentials
The prognostic value of EEG in children with minor head trauma
Sheldrick, G.
The structure of tripeptidyl peptidase I (TPP1) provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis
Siegler, N.
Severe generalized neuropathy in an 18-year-old patient with hereditary sensory-motor polyneurpathy (HMSN) type 1 treated with vincristine due to acute leukemia
Sifringer, M.
Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission
Smitka, M.
Postinfectious autoimmune-mediated encephalitis versus relapse of herpes encephalitis?
Muscular magnet resonance imaging (M-MRI) in α-Dystroglykanopathies – clinical course of two juvenile patients with LGMD2I and LGMD2M
Sorantin, E.
20 years evaluation of pediatric patients with encephalitis in the PICU
Sörensen, N.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients
Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Sperl, W.
Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue
Diagnostic strategy in mitochondrial disorders – An update
Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations
Improved molecular diagnostics for patients with respiratory chain complex deficiency
Spiczak, S. von
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data
Sprinz, A.
Focal dystonia of dominant hand in a 13 year old girl: Action dystonia successfully treated by botulinumtoxine A (Xeomin®)
Multimodal treatment of Cerebral Palsy (CP) including physical therapy, Botulinumtoxin und Lokomat-Training: A case report
Treatment of cerebral palsy: Use of botulinum neurotoxin type A free of complexing proteins (Xeomin®) in childhood
Stark, W.
Natalizumab in 4 cases of pediatric multiple sclerosis
Staudt, M.
Hemiplegic migraine with cerebellar atrophy: A second pediatric case
Early determination of somatosensory cortex
Stefovska, V. G.
Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission
Steichen-Gersdorf, E.
Cardiac arrest in a patient with glutaric aciduria type II
Steinborn, M.
Hennekam-syndrome with unusual MRI-changes and symptomatic epilepsy
Steinfeld, R.
Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency
The structure of tripeptidyl peptidase I (TPP1) provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis
Steinlin, M.
Bannwarth's syndrome – A rare but important manifestation of neuroborreliosis in childhood
Therapy of sinus venous thrombosis in childhood – A standardised treatment protocol – Call for participation
Stenger, R. D.
Outcome of endoscopic therapy of complex hydrocephalus
Stephani, U.
Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data
Stöcklin, B.
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Stolle, S.
Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?
Stoltenburg-Didinger, G.
Neuropathologic findings in patients with primary autosomal recessive microcephaly
Storch, S.
Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship
Stötter, M.
Polyneuropathy and hepatopathy as an infantile manifestation of a POLG1 gene defect
Strobl, R.
Uncommon manifestations of childhood neuroborreliosis
Stülpnagel, C. von
Intracerebral calcification in a newborn – Not always a connatal infection
Stupp, N.
Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?
Stütz, A.
Imino analogues of galactose: Inhibitors of human acid β-D-Galactosidase and putative pharmacological chaperones for the treatment of GM1-Gangliosidosis
Syrbe, S.
Seizures caused by accidental dimenhydriante intoxication
Toxic effects of lamotrigine ingestion in children
Miller Fisher syndrome and Guillain Barré syndrome with ophtamloplegia: Two cases with overlapping phenotype
Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig
Chronic fatigue and pain syndrome caused by persistent intoxication with cactus spurge in a 12-year-old girl
Tacke, U.
Wernicke encephalopathy in childhood
Taeuber, A.
Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?
Telegravciska, M.
Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia
Tesarova, M.
Improved molecular diagnostics for patients with respiratory chain complex deficiency
Thoms, K.
Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity
Timmann-Braun, D.
Ataxia with oculomotor apraxia 1 (AOA1) in a consanguineous Pakistanian familiy
Tinschert, S.
Pontine tegmental cap dysplasia: Two additional cases
Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report
Trefz, F. K.
Neonatal encephalitis through human parechoviruses with signs of extensive white matter injury – Case study and comparison to existing published cases
Trimmel-Schwahofer, P.
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Tro-Baumann, B.
Provocation of seizures by vaccination with children suffering from SCN1A-mutation
Trollmann, R.
Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report
Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)
Tsiakas, K.
Treatment of NPC with miglustat in Germany
Manifestation and diagnosis of NPC disease in Germany
Tuglaci, S.
Modified memory processes in children with febrile seizures: Analysis of event-related potentials
Turski, L.
Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission
Tyshchenko, N.
Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report
Uhl, M.
Wernicke encephalopathy in childhood
Uhlig, H.
Seizures caused by accidental dimenhydriante intoxication
Ullrich, K.
Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship
Urak, L.
Surgery during early life in children with intractable epilepsy – A prospective evaluation
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Utzig, N.
Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity
van Baalen, A.
VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data
van Kempen, M. J. A.
VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data
Vargha-Khadem, F.
Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI
Vass, K.
Epidemiology of pediatric multiple sclerosis in Austria
Vater, D.
Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient
Acute motor and sensory axonal neuropathy (AMSAN) in a 7-year-old boy. A cases report
Deep brain stimulation in children and adolescents with dystonia
IAHSP caused by maternal uniparental isodisomy in ALS2
GLUT1 deficiency in a child with a movement disorder
Verney, C.
Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease
Vester, U.
Copper histidine therapy started in a boy at the age of three years – Treatment option for a mild form of Menkes's disease
Vianey-Saban, C.
Cardiac arrest in a patient with glutaric aciduria type II
Vincent, A.
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder
Vogrinec, G.
The Preserved Speech Variant of Rett syndrome: Specificity of atypicality?
Voigt, B.
Self regulation in preterms – preliminary data with regard to the assessment of „Effortful Control“
Wagenstaller, J.
Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia
Waibel, P.
Citrobacter koseri meningitis – A rare and severe disease in the neonate. A case report
Walden, U.
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder
Walkinshaw, G.
Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)
Waltz, S.
Patients with Dravet's syndrome and SCN1A-mutation with a benign course of illness – A case report with 6 patients
Warmuth-Metz, M.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients
Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Low grade glioma in pediatric NF-1 patients
Weber, P.
Acute disseminated encephalomyelitis review in 8 pediatric patients
Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome
Weber, Y.
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
Wedekin, M.
Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure
Weglage, J.
Focal dystonia of dominant hand in a 13 year old girl: Action dystonia successfully treated by botulinumtoxine A (Xeomin®)
Treatment of cerebral palsy: Use of botulinum neurotoxin type A free of complexing proteins (Xeomin®) in childhood
Wehrli, E.
Therapy of sinus venous thrombosis in childhood – A standardised treatment protocol – Call for participation
Weigel, C.
Outcome of endoscopic therapy of complex hydrocephalus
Weise, A.
Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia
Weise, D.
Cyclic Esotropia – A rare differenzial diagnosis in non paralytic strabismus in childhood
Weise, S.
Sandifers syndrome – Unusual case report and review of the literature
Dystonic movements and developmental coordination disorder – Successful treatment with methylphenidate
Weissert, M.
Citrobacter koseri meningitis – A rare and severe disease in the neonate. A case report
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Acute basilar artery thrombosis in childhood: A therapeutic dilemma
Outcome of acute peripheral facial palsy in children – A catamnestic study of 84 patients
Wendelin, G.
Febrile seizures – First symptom of Rasmussenencephalitis
Homocystein as an important diagnostic marker of remethylation defects – A case report
Wenzel, D.
Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report
Westhoff, B.
Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up
Wiegand, C.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients
Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Wilke, M.
Clinical course of two siblings with Metachromatic Leukodystrophy (MLD) with and without Stem cell transplantation (SCT)
A new score for assessing white matter changes in metachromatic leukodystrophy
Winter, P.
IAHSP caused by maternal uniparental isodisomy in ALS2
Wittig, I.
mitoNET – German Network for mitochondrial disorders
Wochner, K.
Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)
Woermann, F.
A series of 34 patients with Rasmussen's encephalitis: Clinical course, EEG- and MRI findings
Wolf, N.
Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report
Deep brain stimulation in children and adolescents with dystonia
IAHSP caused by maternal uniparental isodisomy in ALS2
GLUT1 deficiency in a child with a movement disorder
Atypical clinical presentation of a girl with episodic ataxia type II
Wolf, N. I.
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Wrodnigg, T.
Imino analogues of galactose: Inhibitors of human acid β-D-Galactosidase and putative pharmacological chaperones for the treatment of GM1-Gangliosidosis
Wudy, S.
Oxcarbazepine accelerates steroid elimination in young men with epilepsy due to cytochrome P450 3A4 induction
Zabel, C.
Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission
Zeiner, F.
Hemiplegic migraine with cerebellar atrophy: A second pediatric case
Zernikow, B.
Quantitative Sensory Testing (QST) in children and adolescents
Zobel, G.
20 years evaluation of pediatric patients with encephalitis in the PICU
Plasmapheresis in the treatment of pediatric patients with neurological diseases: 10 years experience
Zotter, S.
Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)
Zürcher, C.
Natalizumab in 4 cases of pediatric multiple sclerosis
Zwiener, I.
Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients
Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up
Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents
Zwirner, A.
Neuropathologic findings in patients with primary autosomal recessive microcephaly