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Nederlands Tijdschrift Voor Geneeskunde|April 3, 2008
[Familial hemiplegic migraine resulting in recurrent coma]H Lee, M Aramideh, H B Ginjaar
Nederlands Tijdschrift Voor Geneeskunde|June 10, 2004
[From gene to diseases; hypokalemic periodic paralysis]T P Links, H B Ginjaar, J H van der Hoeven
Biochimica Et Biophysica Acta|May 23, 1978
Amino acid incorporation in a cell-free system derived from rat liver studied with the aid of selenodiglutathioneL N Vernie, H B Ginjaar, I T Wilders, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 6, 2005
[The spectrum of hereditary skeletal-muscle channelopathies]J Trip, G Drost, H B Ginjaar, et al.
Nederlands Tijdschrift Voor Geneeskunde|December 2, 2006
[A girl with hereditary myotonia due to an exceptional sodium channel mutation]J C van den Bergen, K T Verbruggen, H B Ginjaar, et al.
Neuropediatrics|August 2, 2008
Thought ripples on muscle waves: recognition of rippling muscle diseaseN C Voermans, N van Alfen, G Drost, et al.
Neurogenetics|October 31, 2009
Isolated eyelid closure myotonia in two families with sodium channel myotoniaB C Stunnenberg, H B Ginjaar, J Trip, et al.
Journal of Neurology|March 3, 2009
Health status in non-dystrophic myotonias: close relation with pain and fatigueJ Trip, J de Vries, G Drost, et al.
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