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Neurology
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Abstracts of the 35th Annual Meeting of the Society of Neuropediatrics
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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