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Abstracts of the 38th Annual Meeting of the Society of Neuropediatrics
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Nagarajah, J
A 16 year-old patient presenting with Lambert-Eaton myasthenic syndrome
Nallinger, A
Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis
Nastulla, T
Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis
Nathrath, M
An opel-label, multi-center, expanded access study of RAD001 (Everolimus) in patients with TSC SEGA
Navarro-Ramirez, L
3D-Television and the Risk of Seizures in Children
Nebgen, S
Bannayan-Riley-Ruvalcaba-syndrom – an unusual differential diagnosis of dilatated Virchow-Robin spaces
Nelle, W
Epileptic seizures with mild gastroenteritis
Nestrasil, I
Quantitative Brain Volumetric Analysis in Neuronal Ceroid Lipofuscinoses: A tool to precisely monitor disease progression
Neu, A
KCNQ2(NMF134)-mutant mice as a model for severe neonatal epilepsy
Neubauer, B
Ring chromosome 22 and neurofibromatosis type II: proof of two hit model for the loss of the NF2 gene in the development of meningioma
Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity
Characterization of endophenotypes in juvenile idiopathic generalized epilepsies by transcranial magnetic stimulation
Prevalence of Antineuronal Antibodies in Children with Autoimmune Thyreoiditis and/or Encephalitis of Unclear Etiology
Cerebral Thiamine-Transporter-Deficiency (SLC19A3) – A Rare But Treatable Cause Of An Acute Necrotizing Encephalopathy
Neubert, G
Microcephaly and Effects of Cdk5rap2 Downregulation in Murine Embryonic Stem Cells
Neuhann, T
Narrowing down the minimal critical region for epilepsy susceptibility in chromosome 5p
Neumann, H
Neurocognitive testing of very low birth weight infants at an age of 4 years
Niederstadt, T
Is neuritis nervi optici in children a predictor of multiple sclerosis in adulthood?
CNS vasculitis as early manifestation of polyarteritis nodosa
Ninnemann, O
Microcephaly and Effects of Cdk5rap2 Downregulation in Murine Embryonic Stem Cells
Noachtar, S
Presurgical evaluation in refractory epilepsy in toddlers with depths electrodes
Nögel, S
Pyruvate dehydrogenase deficiency: Novel PDHA1 mutation in a child with progressive encephalopathy
Nolte, K
FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment
NolteBuchholtz, S
Measuring quality of life in patients with life-limiting neuromuscular disorders: a pilot study using the Kidscreen-27- and KINDL-R-questionnaire