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 (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
Y
Z
Bader, I.
Reversible Epileptic Encephalopathy upon Uridine Treatment in Patients with CAD Mutations
Badura, K.
Cerebral Imaging (CT/MRI): Consequences for Neurorehabilitation
Baig, S. M.
Mutations in KIF14, Encoding Kinesin-Like Protein KIF14, Cause Primary and Syndromic Microcephaly
Bak-Göcke, U.
Guillain-Barré syndrome: Two Cases with Serious and Atypical Process
Balci, M.
Paroxysmal Extreme Pain Disorder in a Girl at the Age of Three Months, Confirmed by Mutation of the SCN9A Gene
Ballhausen, D.
Clinical Presentation and Molecular Findings in Two Index Patients with GM2 Gangliosidosis/Mb. Sandhoff
Bangert, H.
Development of a Classification System for Wheelchair Maintenance and Seat Positioning
Baric, I.
NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood
Bartels, Baz M.
What Is the Right Pressure of Shunt Valves in Newborns?
Bartholdi, D.
Northern Epilepsy: Not So Northern Anymore
Bartsch, S.
Novel Homozygous Missense Mutation in ALDH7A1 Causes Neonatal Pyridoxine-Dependent Epilepsy
Bauder, F.
Severe Cortical Malformation and Acquired Cataract: An Unusual Presentation of DYNC1H1 Mutation in Twins
Baumann, M.
Perampanel Add-on Therapy for the Treatment of Children and Adolescents with Partial and Primary Generalized Seizures: A Report from the University Hospital of Innsbruck
Neuromyelitis Optica Spectrum Disorders in Pediatric Patients
Baumgartner, J.
Perampanel Add-on Therapy for the Treatment of Children and Adolescents with Partial and Primary Generalized Seizures: A Report from the University Hospital of Innsbruck
Baumgartner, S.
Neuromyelitis Optica Spectrum Disorders in Pediatric Patients
Bayha, U.
Early Effects after Hematopoietic Stem Cell Transplantation in 13 Children with Juvenile Metachromatic Leukodystrophy
Baz, M. Bartels
Prognosis and Neurologic Outcome in Shaken Baby Syndrome
Becher, T.
“I See Something You Don’t See...”: Cerebral Visual Impairment in Children with Cerebral Palsy
Beckmann, A.
Globotriaosylsphingosine (Lyso-GB3 bzw. Lyso-GL3), an Excellent Biomarker for Children with Fabry Disease
Beez, T.
GAD65-Positive Limbic Encephalitis and Large Temporal Arachnoid Cyst: A Diagnostic Conundrum
Bender, B.
Early Effects after Hematopoietic Stem Cell Transplantation in 13 Children with Juvenile Metachromatic Leukodystrophy
Benet-Pagès, A.
CNV Detection from Targeted Next-Generation Panel Sequencing Data Increases the Diagnostic Yield in Patients with Neuromuscular Diseases
Bennett, C. F.
Interim Efficacy and Safety Results from the Phase 3 ENDEAR Study of Nusinersen in Infants Diagnosed with Spinal Muscular Atrophy (SMA)
Bennett, C Frank
Efficacy and safety of nusinersen in children with later-onset spinal muscular atrophy (SMA): results of the phase 3 CHERISH study
Berkowitz, N.
Predictors of Efficacy in Patients with Adjunctive Everolimus Therapy for Treatment-Resistant Seizures Associated with Tuberous Sclerosis Complex
Berner, R.
Effects of Janus Kinase Inhibition in Two Children with Aicardi-Goutières Syndrome
Bernius, P.
GOAL: Gait Outcome Assessment List
Berweck, S.
Long-Term Outcome after Vegetative State Due to Near-Drowning and Quality of Life of the Families
GOAL: Gait Outcome Assessment List
Early-Phase Rehabilitation of Children and Adolescents with Chronic Disorders of Consciousness: Standardized, Ability-Based Registration of Remission (RemiPro) Supports Goal-Finding and Establishing a Prognosis
Cerebral Imaging (CT/MRI): Consequences for Neurorehabilitation
Development of a Classification System for Wheelchair Maintenance and Seat Positioning
A Technical Neuro-Orthopedic and Neuropediatric Report on Requirements Needed for a Successful Rehabilitation of a Disabled Adolescent
Learning to Cope with Mirror Movements in Activities of Daily Living: Effects of Targeted Bimanual Therapy in Children with Unilateral Spastic CP
Improving the Quality of Care in the Specialization: The Benefits of “Hands-on” Courses for Learning Neuromuscular Ultrasound
Beschle, J.
Early Effects after Hematopoietic Stem Cell Transplantation in 13 Children with Juvenile Metachromatic Leukodystrophy
Beste, C.
Cognition in Neurofibromatosis Type 1: What We Know and What We Do Not
Betzler, C.
Reversible Epileptic Encephalopathy upon Uridine Treatment in Patients with CAD Mutations
Bevot, A.
Early Effects after Hematopoietic Stem Cell Transplantation in 13 Children with Juvenile Metachromatic Leukodystrophy
Bigi, S.
Transient Ischemic Attack (TIA): A Problem Not to Miss
Northern Epilepsy: Not So Northern Anymore
Biskup, S.
Emery-Dreifuss Muscular Dystrophy Type 1 in a 15-Year-Old Patient Due to a Novel Putative Splice-Site Mutation
Blankenburg, M.
The Detection and Therapy of Pain in Children and Adolescents with Life-Threatening Neuropediatric Disorder
Time Is Brain: Thrombectomy after Pediatric Stroke in Two Previously Healthy Girls
Bley, A.
Compassionate Use of Simvastatin for a Patient with Juvenile Metachromatic Leukodystrophy
The Natural History of Canavan Disease: Description of 23 New Cases and Comparison with Literature
Bluschke, A.
Cognition in Neurofibromatosis Type 1: What We Know and What We Do Not
Blüthner, M.
Muscle Dystrophy Differential Diagnosis: Manifestation of Anti-HMG-CoA Reductase Antibody Myositis in Infancy
Bode, H.
Leigh Syndrome Caused by a Novel Gene Variant in NDUFS8
Bohnenpoll, J.
The Natural History of Canavan Disease: Description of 23 New Cases and Comparison with Literature
Boltshauser, E.
Joubert Syndrome
4H Leukodystrophy: A Rare Movement Disorder
Bonikowski, M.
Time to Retreatment after AbobotulinumtoxinA (Dysport) Injections in Children with Dynamic Equinus Foot Deformity
Abobotulinumtoxin-A (DYSPORT) Injection Doses per Muscle in Pediatric Patients with Lower Limb Spasticity
Phase 3 Trial to Evaluate AbobotulinumtoxinA (Dysport) Injections in Children with Upper Limb Spasticity Due to Cerebral Palsy: A Study Design
Boor, R.
Evaluation of the Effects of Anticonvulsive Therapy in Children with Symptomatic Epilepsy by a State Space Modeling Approach
Brackmann, F.
Histopathological Proof of the Pathogenetic Role of a Rare GFAP Mutation in Alexander´s Disease with Isolated Flaccid Paraparesis
Compound Heterozygous RYR1 Mutation in a Preterm with Arthrogryposis and Core Myopathy with Prenatal CNS Bleedings
Brandl, U.
Mechanisms of Age-Dependent Increase of Perisylvian Cortical Excitability
Brandsma, R.
Motor Function in Pediatric ALL Survivors after Chemotherapy-Only
Bremova, T.
Niemann-Pick Type C: Typical Ocular Motor Findings and Red Flags
Brockmann, K.
Acute and Episodic Movement Disorders: ATP1A3-Related Disorders as Differential Diagnosis
The Acquisition of Rare Neurological Disorders in Childhood (”ESNEK”): First Interim Results after 2 Years
FOXG1 Syndrome: Genotype–Phenotype Association in 84 Patients with FOXG1 Variants
Brösse, I.
Niemann-Pick Type C Disease: A Challenge in Diagnostics, Therapy, and Care for Affected Families
Severe Course of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) with Detection of an Unknown Antineuronal Antibody
Brunner-Krainz, M.
4H Leukodystrophy: A Rare Movement Disorder
Budde, B.
Mutations in KIF14, Encoding Kinesin-Like Protein KIF14, Cause Primary and Syndromic Microcephaly
Bulst, S.
Titinopathies in Human Genetics Diagnostics
CNV Detection from Targeted Next-Generation Panel Sequencing Data Increases the Diagnostic Yield in Patients with Neuromuscular Diseases
Bürki, S.
Northern Epilepsy: Not So Northern Anymore
Buyken, A.
Lunch and Cognitive Performance in School Children: The Crossover Intervention Trial CogniDo