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Neuromuscular Disorders : NMD|February 21, 2006
A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosisPascal Laforêt, Pascale Richard, Mina Ait Said, et al.
Neuromuscular Disorders : NMD|March 8, 2016
Atrial flutter in myotonic dystrophy type 1: Patient characteristics and clinical outcomeKarim Wahbi, Frederic A Sebag, Nicolas Lellouche, et al.
Stem Cell Research|February 19, 2026
Generation and characterization of two human induced pluripotent stem cell lines from patients with Danon diseaseMatthieu Lejars, Christelle Kabore, Benjamin Marande, et al.
Heart (British Cardiac Society)|June 23, 2026
Cardiac and extracardiac outcomes after heart transplantation in laminopathiesGauthier Giordano, Guillaume Coutance, Karim Wahbi, et al.
Stem Cell Research|September 4, 2025
Generation and characterization of three human induced pluripotent stem cell lines from patients with glycogen storage disease type IIMatthieu Lejars, Christelle Kabore, Benjamin Marande, et al.
Neuromuscular Disorders : NMD|July 28, 2016
Cross-sectional retrospective study of muscle function in patients with glycogen storage disease type IIIValérie Decostre, Pascal Laforêt, Aleksandra Nadaj-Pakleza, et al.
European Heart Journal|October 23, 2010
Acute coronary syndrome in human immunodeficiency virus-infected patients: characteristics and 1 year prognosisFranck Boccara, Murielle Mary-Krause, Emmanuel Teiger, et al.
Annals of Neurology|June 27, 2013
Polyglucosan body myopathy caused by defective ubiquitin ligase RBCK1Johanna Nilsson, Benedikt Schoser, Pascal Laforet, et al.
Molecular Genetics and Metabolism|September 11, 2017
Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIaValérie Decostre, Pascal Laforêt, Marie De Antonio, et al.
Archives of Cardiovascular Diseases|October 22, 2013
Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1Karim Wahbi, Vincent Algalarrondo, Henri Marc Bécane, et al.
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