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Nederlands Tijdschrift Voor Geneeskunde|April 3, 2008
[Familial hemiplegic migraine resulting in recurrent coma]H Lee, M Aramideh, H B GinjaarNederlands Tijdschrift Voor Geneeskunde|June 10, 2004
[From gene to diseases; hypokalemic periodic paralysis]T P Links, H B Ginjaar, J H van der HoevenBiochimica Et Biophysica Acta|December 19, 1975
Elongation factor 2 as the target of the reaction product between sodium selenite and glutathione (GSSeSG) in the inhibiting of amino acid incorporation in vitroL N Vernie, W S Bont, H B Ginjaar, et al.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.Nederlands Tijdschrift Voor Geneeskunde|January 9, 1993
[Application of combined DNA and dystrophin protein analysis in the diagnosis of Duchenne's and Becker's muscular dystrophy in 102 Dutch patients]H B Ginjaar, E Bakker, H F Busch, 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.Pageof 4