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 38th 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
Q
R
S
T
U
V
W
Y
Z
Ü
Machuta, K
Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis
Mainberger, F
Attention deficit in patients with Noonan Syndrome (NS)
Makhani, N
Hiccups, Vomiting and the Brain
Mall, V
Hypocretin-level during therapy with intravenous immunglobulines in an early stage of narcolepsy with cataplexy in childhood
Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia
Macrocerebellum: not a clinical and neuroimaging entity
Attention deficit in patients with Noonan Syndrome (NS)
Acetazolamide as treatment for GLUT1 deficiency syndrome?
Mallmann, R
Subacute sclerosing panencephalitis
Marquardt, T
Treatment of infantile Pompe s disease with enzyme replacement therapy in Germany and Austria
Massot Taurus, A
Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity
Maxonus, I
Intranasal insulin may influence motor activities and behaviour in Phelan McDermid Syndrom
May, T
Burdens of parents with epileptic children – Results of a study using a short-form of the German version of the Impact-on-Family-Scale
Mayatepek, E
Sudden bilateral sensorineural deafness in a 5 years old girl with blue sclerae, keratoconus, hypermobility of the joints and hyperelasticity of the skin with a mutation in the ZNF469 gene encoding for Brittle-Cornea-Syndrome
Brown-Vialetto-Van Laere syndrome: A riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene
Mayer, T
Valproate induced nocturnal enuresis – a seldom side effect?
Mayr, J
Pyruvate dehydrogenase deficiency: Novel PDHA1 mutation in a child with progressive encephalopathy
Meier, T
DELOS Phase III Study with Idebenone (Catena®) in Duchenne Muscular Dystrophy
Meitinger, T
Mitochondrial Encephalopathies caused by defective mitochondrial translation
Mellies, U
Myasthenic symptoms: From initial presentation to diagnosis
Mengel, E
Respiration and its correlation with motoric function in non-classic Pompe disease
Treatment of infantile Pompe s disease with enzyme replacement therapy in Germany and Austria
Merfort, J
Neuroborreliosis as a chameleon – mimicking tuberculous meningitis
Merkenschlager, A
Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?
Shaking the head without end – bobble-head doll syndrome in no-no direction
Meyer, S
The role of Cochrane reviews in child neurology: A systematic analysis
Melatonin does not influence sleep-deprivation electroencephalogram recordings in children
Middelhoff, C
Symptomatic Treatment of Tomaculous Polyneuropathy with Methylprednisolone
Milkereit, D
KCNQ2(NMF134)-mutant mice as a model for severe neonatal epilepsy
Miny, P
Mosaic ring chromosome 3 in a child with epilepsy and developmental delay
Möllers, M
Microcephaly – Capillary Malformation Syndrome: A new syndrome with severe epilepsy – the first german patient
Moll-Khosrawi, P
Statistical properties of the jNCL scoring system according to Kohlschütter (1988)
Moog, U
Encephalocraniocutaneous lipomatosis (ECCL) – a case report
Morellini, F
KCNQ2(NMF134)-mutant mice as a model for severe neonatal epilepsy
Morris-Rosendahl, D
Microcephaly – Capillary Malformation Syndrome: A new syndrome with severe epilepsy – the first german patient
Muehlhausen, C
Pseudotumor cerebri in an 8 month old infant
Mueller, A
Visual diagnosis of Morbus Niemann Pick Typ C
Mueller, G
Validity of the clinical neurological state and nerve conduction velocity in diagnosing diabetic peripheral neuropathy
Muhle, H
Clinical characterization of myoclonic-astatic epilepsy
The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology
Müller, A
Long-term Outcome after Vegetative State due to Near-Drowning and Quality of Life of the Families
Müller, I
Stem cell transplantation (SCT) in metachromatic leukodystrophy (MLD) – results from 9 patients
Müller, M
Tick-borne encephalitis: four cases in young vaccinated children
CT Perfusion and CT Angiography in children and juvenile patients during an attack of migraine with aura
Müller-Felber, W
Familial mutation in ACTA1 gene – clinical variability
Multiple sclerosis and periodic fever syndromes: Characterization of clinical symptoms
Munteanu, M
Mutation in the Fukutin-Gene (FKTN) as cause of a mild congenital muscular dystrophy
Myasthenic symptoms: From initial presentation to diagnosis
Deletion 22q13 (Phelan-McDermid-Syndrom) in two children with delayed development of speech and muscular hypotonia
Münter, S
Symptomatic Treatment of Tomaculous Polyneuropathy with Methylprednisolone
Muntoni, F
A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome
Møller, R
The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology