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Acta Myologica, ISSN 1128-2460, 03/2018, Volume 37, Issue 1, p. 1
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 03/2018, Volume 28, Issue 3, pp. 300 - 301
Journal Article
Acta Myologica, ISSN 1128-2460, 2016, Volume 35, Issue 2, pp. 96 - 99
Journal Article
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, ISSN 1128-2460, 12/2015, Volume 34, Issue 2-3, pp. 93 - 94
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 12/2018, Volume 136, Issue 12, pp. 1425 - 1426
Journal Article
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 12/2017, Volume 36, Issue 4, p. 199
Myotonic dystrophy type 1 is a multisystemic disorder characterized by myotonia, muscle weakness and involvement of several organs and apparatus such as heart,... 
Journal Article
Trends in Cardiovascular Medicine, ISSN 1050-1738, 07/2018, Volume 28, Issue 5, pp. 330 - 337
Muscular dystrophy (MD) connotes a heterogeneous group of inherited disordersaffecting skeletal and cardiac muscle. Inseveral forms of MD, the cardiac disease... 
Heart failure | Becker muscular dystrophy | Myotonic dystrophy | Duchenne muscular dystrophy | Fibrosis | Dystrophinopathic cardiomyopathy | Angiotensin-converting enzyme inhibitor | Emery–Dreifuss muscular dystrophy | Muscular dystrophy | CARDIAC & CARDIOVASCULAR SYSTEMS | Emery-Dreifuss muscular dystrophy | HEART-FAILURE | CARDIOMYOPATHIC HAMSTER | ANGIOTENSIN-II | CONVERTING ENZYME-INHIBITORS | CARDIAC INVOLVEMENT | PAROXYSMAL ATRIAL-FIBRILLATION | P-WAVE DURATION | TYPE-1 PATIENTS | MYOTONIC-DYSTROPHY | ELECTROMECHANICAL DELAY | Muscular Dystrophies - metabolism | Humans | Muscular Dystrophies - drug therapy | Cardiomyopathies - prevention & control | Myocardium - pathology | Treatment Outcome | Muscular Dystrophies - complications | Cardiomyopathies - etiology | Disease Progression | Animals | Angiotensin-Converting Enzyme Inhibitors - therapeutic use | Cardiomyopathies - metabolism | Myocardium - metabolism | Cardiomyopathies - diagnosis | Renin-Angiotensin System - drug effects | Muscular Dystrophies - diagnosis | Disease Models, Animal | Hypertension | Cardiac arrhythmia | Enzymes | Cardiac muscle | Cardiomyopathy | Patients | Coronary artery disease | Skeletal muscle | Proteins | Studies | Musculoskeletal system | Rodents | Collagen | Cardiac function | Angiotensin | Myocardium | Mutation | Dystrophy | Angiotensin II | Heart diseases | Myopathy
Journal Article
Journal of Cardiovascular Electrophysiology, ISSN 1045-3873, 01/2016, Volume 27, Issue 1, pp. 65 - 72
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2014, Volume 9, Issue 10, p. e108205
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2015, Volume 10, Issue 10, p. e0141240
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2013, Volume 8, Issue 1, p. e52512
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 05/2019, Volume 56, Issue 5, pp. 293 - 300
Background Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder, due to the loss of function of the survival motor neuron (SMN1)... 
salbutamol | spinal muscular atrophy | real-time PCR | double-blind clinical trial | SHAM CONTROL | NUSINERSEN | PILOT TRIAL | GENETICS & HEREDITY
Journal Article
Journal of Interventional Cardiac Electrophysiology, ISSN 1383-875X, 04/2018, Volume 51, Issue 3, pp. 229 - 236
Journal Article
Journal of Cardiovascular Electrophysiology, ISSN 1045-3873, 10/2019
Journal Article