padberg  g.w.
padberg g.w.
hoogleraar neurologie
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Treatment of single brain metastasis: radiotherapy alone or combined with neurosurgery
CJ Vecht, H Haaxma‐Reiche, EM Noordijk, GW Padberg, JHC Voormolen, ...
Annals of Neurology: Official Journal of the American Neurologicalá…, 1993
The choice of treatment of single brain metastasis should be based on extracranial tumor activity and age
EM Noordijk, CJ Vecht, H Haaxma-Reiche, GW Padberg, JHC Voormolen, ...
International Journal of Radiation Oncology* Biology* Physics 29 (4), 711-717, 1994
Localization of the gene for Cowden disease to chromosome 10q22–23
MR Nelen, GW Padberg, EAJ Peeters, AY Lin, B Van den Helm, ...
Nature genetics 13 (1), 114-116, 1996
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy
C Wijmenga, JE Hewitt, LA Sandkuijl, LN Clark, TJ Wright, HG Dauwerse, ...
Nature genetics 2 (1), 26-30, 1992
Germline Mutations in the PTEN/MMAC1 Gene in Patients With Cowden Disease
MR Nelen, WCG Van Staveren, EAJ Peeters, M Ben Hassel, RJ Gorlin, ...
Human molecular genetics 6 (8), 1383-1387, 1997
A unifying genetic model for facioscapulohumeral muscular dystrophy
RJLF Lemmers, PJ Van der Vliet, R Klooster, S Sacconi, P Cama˝o, ...
Science 329 (5999), 1650-1653, 2010
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit
JCTV Deutekom, C Wljmenga, EAEV Tlenhoven, AM Gruter, JE Hewitt, ...
Human molecular genetics 2 (12), 2037-2042, 1993
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2
RJLF Lemmers, R Tawil, LM Petek, J Balog, GJ Block, GWE Santen, ...
Nature genetics 44 (12), 1370, 2012
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy
PGM van Overveld, RJFL Lemmers, LA Sandkuijl, L Enthoven, ...
Nature genetics 35 (4), 315-317, 2003
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4
C Wijmenga, OF Brouwer, P Moerer, GW Padberg, RR Frants, JL Weber
The Lancet 336 (8716), 651-653, 1990
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element
J Gabriels, MC Beckers, H Ding, A De Vriese, S Plaisance, ...
Gene 236 (1), 25-32, 1999
M÷bius syndrome redefined: a syndrome of rhombencephalic maldevelopment
HTFM Verzijl, B van der Zwaag, JRM Cruysberg, GW Padberg
Neurology 61 (3), 327-333, 2003
Novel PTEN mutations in patients with Cowden disease: absence of clear genotype–phenotype correlations
MR Nelen, H Kremer, IBM Konings, F Schoute, AJ van Essen, R Koch, ...
European Journal of Human Genetics 7 (3), 267-273, 1999
Transient loss of consciousness: the value of the history for distinguishing seizure from syncope
WAJ Hoefnagels, GW Padberg, J Overweg, EA Van der Velde, RAC Roos
Journal of neurology 238 (1), 39-43, 1991
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere
RJLF Lemmers, P de Kievit, L Sandkuijl, GW Padberg, GJB van Ommen, ...
Nature genetics 32 (2), 235-236, 2002
Facioscapulohumeral disease
GW Padberg
Leiden: University of Leiden, 243, 1982
Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C
M Auer-Grumbach, A Olschewski, L Papić, H Kremer, ME McEntagart, ...
Nature genetics 42 (2), 160, 2010
Diagnostic criteria for facioscapulohumeral muscular dystrophy
GW Padberg, PW Lunt, M Koch, M Fardeau
Neuromuscular disorders 1 (4), 231-234, 1991
Experienced fatigue in facioscapulohumeral dystrophy, myotonic dystrophy, and HMSN-I
JS Kalkman, ML Schillings, SP Van Der Werf, GW Padberg, MJ Zwarts, ...
Journal of Neurology, Neurosurgery & Psychiatry 76 (10), 1406-1409, 2005
Lhermitte‐Duclos disease and Cowden disease: a single phakomatosis
GW Padberg, JDL Schot, GJ Vielvoye, GTAM Bots, FC De Beer
Annals of Neurology: Official Journal of the American Neurologicalá…, 1991
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