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Person

Prof.dr. G.W.A.M. Padberg

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Update Persondata

Expertise	Clinical neurology; Neuromuscular disorders; Neurogenetics; Neuro-oncology
Expertise (NL)	Klinische neurologie; Neuromusculaire ziekten; Neurogenetica; Neuro-oncologie
Digital Author ID	info:eu-repo/dai/nl/06899897X
Addition	Chairman Department of Neurology, University Medical Centre St Radboud, Nijmegen; Voorzitter Stichting Onderzoek Neuromusculaire Ziekten; Medisch Adviseur Vereniging Spierziekten Nederland; Scientific Advisory Board: FSHD Society (USA); Lid Wetenschapscommissie UMC St Radboud; Lid IKO-werkgroep Neuro-oncologie

Active as

Professor
Organisation	Department of Neurology (RU)
Chair (EN)	Clinical neurology
Chair (NL)	Neurologie
Email	G. Padberg -at- neuro. umcn. nl

Publications

A unifying genetic model for facioscapulohumeral muscular dystrophy.
Facioscapulohumerale spierdystrofie
Clinical features of facioscapulohumeral muscular dystrophy 2.
Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathy.
Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C.

All publications..

Completed research projects

(the most recent research is at the top)
Supervisor	Congenital Cranial Dysinnervation Disorders. A genetic perspective into hereditary congenital facial paresis and Möbius syndrome

Classification

A70000	Public health and health care
D23120	Oncology
D23231	Neurology

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