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Archives of Cardiovascular Diseases|March 21, 2021
Management and outcomes of hypertrophic cardiomyopathy in young adultsÉmilie Baron, Nicole Karam, Erwan Donal, et al.JAMA|March 29, 2012
Electrophysiological study with prophylactic pacing and survival in adults with myotonic dystrophy and conduction system diseaseKarim Wahbi, Christophe Meune, Raphaël Porcher, et al.European Journal of Medical Research|July 24, 2023
French recommendations for the management of glycogen storage disease type IIICamille Wicker, Aline Cano, Valérie Decostre, et al.Stem Cell Research|February 14, 2024
Generation of human induced pluripotent stem cell lines from five patients with Myofibrillar myopathy carrying different heterozygous mutations in the DES genePierre Joanne, Yeranuhi Hovhannisyan, Alexandre Simon, et al.Journal of Neuromuscular Diseases|August 20, 2025
Association between exon-skipping therapy with eteplirsen and cardiac outcomes in Duchenne muscular dystrophyJoel Iff, Isabelle Desguerre, Yunjuan Liu, et al.Archives of Cardiovascular Diseases|May 18, 2024
Target population for a selective cardiac myosin inhibitor in hypertrophic obstructive cardiomyopathy: Real-life estimation from the French register of hypertrophic cardiomyopathy (REMY)Alessandro Parodi, Tania Puscas, Patricia Réant, et al.European Heart Journal|July 31, 2015
Long-term cardiac prognosis and risk stratification in 260 adults presenting with mitochondrial diseasesKarim Wahbi, Wulfran Bougouin, Anthony Béhin, et al.Journal of Inherited Metabolic Disease|October 26, 2019
Incidence and predictors of total mortality in 267 adults presenting with mitochondrial diseasesConstantinos Papadopoulos, Karim Wahbi, Anthony Behin, et al.Neuromuscular Disorders : NMD|December 14, 2011
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal studyKarim Wahbi, Anthony Béhin, Philippe Charron, et al.Journal of Inherited Metabolic Disease|November 26, 2019
A high prevalence of arterial hypertension in patients with mitochondrial diseasesCaroline Chong-Nguyen, Caroline Stalens, Yves Goursot, et al.Pageof 13