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Journal of Molecular Medicine (Berlin, Germany)|September 11, 2025
Dilated cardiomyopathy in patients with PRDM16 haploinsufficiencyClarisse Billon, Gilles Millat, Adeline Goudal, et al.
Plos One|April 28, 2016
Natural History of Cardiac and Respiratory Involvement, Prognosis and Predictive Factors for Long-Term Survival in Adult Patients with Limb Girdle Muscular Dystrophies Type 2C and 2DAbdallah Fayssoil, Adam Ogna, Cendrine Chaffaut, et al.
Heart (British Cardiac Society)|November 28, 2017
Lamin and the heartGabriella Captur, Eloisa Arbustini, Gisèle Bonne, et al.
Circulation. Cardiovascular Genetics|June 15, 2017
Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart RegistryCaroline Chong-Nguyen, Karim Wahbi, Vincent Algalarrondo, et al.
Arthritis and Rheumatism|May 7, 2011
Prediction of pulmonary hypertension related to systemic sclerosis by an index based on simple clinical observationsChristophe Meune, Jérôme Avouac, Paolo Airò, et al.
Journal of Neuromuscular Diseases|April 5, 2021
Improved Cardiac Outcomes by Early Treatment with Angiotensin-Converting Enzyme Inhibitors in Becker Muscular DystrophyCaroline Stalens, Leslie Motté, Anthony Béhin, et al.
Steroids|September 16, 2025
Mineralocorticoid receptor antagonism of vamorolone: Evidence from LIONHEART and VISION-DMD clinical trialsAna de Vera, Paula R Clemens, Utkarsh J Dang, et al.
Heart Failure Clinics|November 15, 2021
Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic OptionsMichele Lioncino, Emanuele Monda, Martina Caiazza, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|May 22, 2026
Heart failure guideline-directed medical therapy in young adults with dystrophin-related cardiomyopathy: the HOPE-MD registryLuca Monzo, Emanuele Bobbio, Giulia Montrasio, et al.
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.
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