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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.Pageof 16