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Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|May 21, 2008
Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up studyDulce Brito, Pascale Richard, Michel Komajda, et al.
Current Opinion in Neurology|September 16, 2004
Congenital myasthenic syndromesDaniel Hantaï, Pascale Richard, Jeanine Koenig, et al.
International Journal of Medical Sciences|March 9, 2026
LAP2 Isoform Profile in Heart Ageing and in Cardiac Cell Proliferation and Differentiation: Input From CRISPR-Cas9-mediated LAP2a Knockdown in H9C2Nathalie Vadrot, Maryline Moulin, Ana Ferreiro, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|May 8, 2007
A familial form of conduction defect related to a mutation in the PRKAG2 genePhilippe Charron, Marc Genest, Pascale Richard, et al.
Blood Transfusion = Trasfusione Del Sangue|November 15, 2012
Assessment of leucoreduction of sickle cell trait blood: quality of the filtered productKarim Ould Amar, Olivier Bourdonné, Sylvie Bruneau, et al.
Pediatric Neurology|September 15, 2010
Novel LMNA mutation presenting as severe congenital muscular dystrophyCynthia Prigogine, Pascale Richard, Peter Van den Bergh, et al.
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|March 11, 2004
Familial hypertrophic cardiomyopathy: the same mutation, different prognosis. Comparison of two families with a long follow-upDulce Brito, Pascale Richard, Richard Isnard, et al.
Neurology India|January 21, 2014
New mutation of the desmin gene identified in an extended Indian pedigree presenting with distal myopathy and cardiac diseaseAtchayaram Nalini, Narayanappa Gayathri, Pascale Richard, et al.
Pflugers Archiv : European Journal of Physiology|December 17, 2013
MYBPC3 in hypertrophic cardiomyopathy: from mutation identification to RNA-based correctionVerena Behrens-Gawlik, Giulia Mearini, Christina Gedicke-Hornung, et al.
Skeletal Muscle|September 28, 2011
ColVI myopathies: where do we stand, where do we go?Valérie Allamand, Laura Briñas, Pascale Richard, et al.
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