Paroxysmal choreoathetosis as presenting symptom of diabetes mellitus.

Por Haan, J, Kremer, H P, Padberg, G W
Publicado em 1989

Dysphagia in inclusion body myositis.

Por Wintzen, A R, Bots, G T, de Bakker, H M, Hulshof, J H, Padberg, G W
Publicado em 1988

Syncope or seizure? The diagnostic value of the EEG and hyperventilation test in transient loss of consciousness.

Por Hoefnagels, W A, Padberg, G W, Overweg, J, Roos, R A, van Dijk, J G, Kamphuisen, H A
Publicado em 1991

A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family.

Por Verzijl, H T, van den Helm, B, Veldman, B, Hamel, B C, Kuyt, L P, Padberg, G W, Kremer, H
Publicado em 1999

Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases.

Por Bakker, E, Van der Wielen, M J, Voorhoeve, E, Ippel, P F, Padberg, G W, Frants, R R, Wijmenga, C
Publicado em 1996

Effects of training and albuterol on pain and fatigue in facioscapulohumeral muscular dystrophy

Por van der Kooi, E. L., Kalkman, J. S., Lindeman, E., Hendriks, J. C. M., van Engelen, B. G. M., Bleijenberg, G., Padberg, G. W.
Publicado em 2007

Clinical features, lectin staining, and a novel GNE frameshift mutation in HIBM

Por Voermans, Nicol C., Guillard, M., Doedée, R., Lammens, M., Huizing, Marjan, Padberg, G.W., Wevers, R.A., van Engelen, B.G., Lefeber, D.J.
Publicado em 2010

Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter

Por Wijmenga, C., Sandkuijl, L. A., Moerer, P., van der Boorn, N., Bodrug, S. E., Ray, P. N., Brouwer, O. F., Murray, J. C., van Ommen, G. J. B., Padberg, G. W., Frants, R. R.
Publicado em 1992

Clinical features of facioscapulohumeral muscular dystrophy 2 [Image: see text]

Por de Greef, J.C., Lemmers, R.J.L.F., Camaño, P., Day, J.W., Sacconi, S., Dunand, M., van Engelen, B.G.M., Kiuru-Enari, S., Padberg, G.W., Rosa, A.L., Desnuelle, C., Spuler, S., Tarnopolsky, M., Venance, S.L., Frants, R.R., van der Maarel, S.M., Tawil, R.
Publicado em 2010

Hypokalemic Periodic Paralysis and the Dihydropyridine Receptor (CACNLIA3): Genotype/Phenotype Correlations for two Predominant Mutations and Evidence for the Absence of a Founder...

Por Elbaz, A., Vale-Santos, J., Jurkat-Rott, K., Lapie, P., Ophoff, R. A., Bady, B., Links, T. P., Piussan, C., Vila, A., Monnier, N., Padberg, G. W., Abe, K., Feingold, N., Guimaraes, J., Wintzen, A. R., van der Hoeven, J. H., Saudubray, J. M., Grunfeld, J. P., Lenoir, G., Nivet, H., Echenne, B., Frants, R. R., Fardeau, M., Lehmann-Horn, F., Fontaine, B.
Publicado em 1995