KNAW

Back to search results
Person

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

Pagina-navigatie:
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

Active as

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

Publications

Facioscapulohumeral muscular dystrophy.
Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy.
Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the families.
Pushing the genetic frontier with facioscapulohumeral muscular dystrophy.
Effects of training and albuterol on pain and fatigue in facioscapulohumeral muscular dystrophy.
All publications..

Current research

(the most recent research is at the top)
Project leader Implementation of EASYcare Assessment in the care for the elderly

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
Update this data

Go to page top
Go back to contents
Go back to site navigation