neuropediatrics
130445
DE
EN
Home
Products
Journals
Books
Book Series
Service
Library Service
Help
Contact
Portal
Neuropediatrics
Full-text search
Full-text search
Author Search
Title Search
DOI Search
Metadata Search
Journal
Aims and Scope
Editorial Board
German National License
Authors
Instructions for Authors
Submit a Manuscript
Resident & Fellow section
Subscription
Subscription Information & Contacts
Institutional Licensing
Society
German Speaking Society of Neuropediatrics (GNP)
NPED Women
Article Collection
About Women In Medicine
Not Logged In
Login
Username or e-mail address:
Password:
Forgot Access Data?
Register Now
OpenAthens/Shibboleth Login
Shopping Cart
Year (Archive)
2024
2024
2023
2022
2021
2020
2019
2018
2017
2016
2015
2014
2013
2012
2011
2010
2009
2008
2007
2006
2005
2004
2003
2002
2001
2000
1999
1998
1997
1996
1995
1994
1993
1992
1991
1990
1989
1988
1987
1986
1985
1984
1983
1982
1981
1980
1979
1978
1977
1976
1975
1974
1973
1972
1971
1970
1969
Issues
Current Issue
Free Sample Issue (01/2024)
Related Journals
Seminars in Neurology
Journal of Neurological Surgery
Indian Journal of Neurosurgery
Indian Journal of Neurotrauma
European Journal of Pediatric Surgery
Journal of Child Science
International Journal of Epilepsy
Related Books
Neurology
Pediatrics
Abstracts of the 35th Annual Meeting of the Society of Neuropediatrics
Abstracts (HTML)
List of Authors
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
R
S
T
U
V
W
Z
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