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Plos One|January 6, 2018
Left bundle branch block in Duchenne muscular dystrophy: Prevalence, genetic relationship and prognosisAbdallah Fayssoil, Rabah Ben Yaou, Adam Ogna, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 20, 2004
Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?Jop H van Berlo, Willem G de Voogt, Anneke J van der Kooi, et al.
Scientific Reports|November 23, 2021
Circulating bile acids concentration is predictive of coronary artery disease in humanCaroline Chong Nguyen, Denis Duboc, Dominique Rainteau, et al.
Archives of Cardiovascular Diseases|December 27, 2016
Patient journey in decompensated heart failure: An analysis in departments of cardiology and geriatrics in the Greater Paris University HospitalsFlorent Laveau, Nadjib Hammoudi, Emmanuelle Berthelot, et al.
Nature Structural & Molecular Biology|June 21, 2011
Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophyFrédérique Rau, Fernande Freyermuth, Charlotte Fugier, et al.
JAMA Neurology|February 7, 2018
Development and Validation of a New Scoring System to Predict Survival in Patients With Myotonic Dystrophy Type 1Karim Wahbi, Raphaël Porcher, Pascal Laforêt, et al.
Journal of the American Heart Association|August 15, 2023
Prognosis of Right Ventricular Systolic Dysfunction in Patients With Duchenne Muscular DystrophyAbdallah Fayssoil, Nicolas Mansencal, Lee S Nguyen, et al.
JAMA Cardiology|September 24, 2025
Electrocardiogram vs Electrophysiological Study and Major Conduction Delays in Myotonic Dystrophy Type 1Nicolas Clementy, Fabien Labombarda, François Grolleau, et al.
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