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The New England journal of medicine, ISSN 1533-4406, 04/2011, Volume 364, Issue 17, pp. 1643 - 1656
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 05/2016, Volume 67, Issue 21, pp. 2533 - 2546
.... Dystrophinopathies include Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD), X-linked dilated cardiomyopathy, as well as DMD and BMD female carriers... 
Cardiovascular | Internal Medicine | muscular dystrophy cardiomyopathy | Becker muscular dystrophy cardiomyopathy | Duchenne muscular dystrophy cardiomyopathy | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Genetic Therapy | Glucocorticoids - therapeutic use | Humans | Cardiomyopathies - genetics | Angiotensin-Converting Enzyme Inhibitors - therapeutic use | Aging | Electrocardiography | Muscular Dystrophy, Duchenne - therapy | Heart-Assist Devices | Adrenergic beta-Antagonists - therapeutic use | Cardiomyopathy, Dilated - genetics | Echocardiography | Heart Transplantation | Arrhythmias, Cardiac - etiology | Magnetic Resonance Imaging, Cine | Disease Progression | Gene Editing | Cardiomyopathies - therapy | Mineralocorticoid Receptor Antagonists - therapeutic use | Dystrophin - genetics | Heterozygote | Muscular Dystrophy, Duchenne - genetics | Mutation | Angiotensin Receptor Antagonists - therapeutic use | Cardiomyopathy, Dilated - therapy | Heart failure | Cardiomyopathy | Mortality | Muscles | Dystrophin | Heart diseases | Cardiovascular agents | Heart | Medical research | Enzymes | Prosthesis | Enzyme inhibitors | Implants, Artificial | Electrocardiogram | Medicine, Experimental | Life expectancy | Genes | Editing | Kinases | Muscular dystrophy | Proteins | Musculoskeletal system | Genotype & phenotype | Rodents | Chromosomes | Age | Deoxyribonucleic acid--DNA | Index Medicus | Abridged Index Medicus
Journal Article
The Lancet (British edition), ISSN 0140-6736, 08/2015, Volume 386, Issue 9995, pp. 813 - 825
Summary Left ventricular non-compaction, the most recently classified form of cardiomyopathy, is characterised by abnormal trabeculations in the left ventricle, most frequently at the apex... 
Internal Medicine | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Cardiomyopathy, Dilated - classification | Echocardiography | Isolated Noncompaction of the Ventricular Myocardium - therapy | Humans | Isolated Noncompaction of the Ventricular Myocardium - classification | Magnetic Resonance Angiography | Anticoagulants - therapeutic use | Male | Treatment Outcome | Arrhythmias, Cardiac - etiology | Signal Transduction - genetics | Mutation - genetics | Animals | Defibrillators, Implantable | Electrocardiography | Cardiomyopathy, Dilated - diagnosis | Female | Mice | Cardiomyopathy, Dilated - therapy | Disease Models, Animal | Isolated Noncompaction of the Ventricular Myocardium - diagnosis | Heart failure | Heart | Genetic disorders | Cardiomyopathy | Heart diseases | Jaw | Regulators | Embryo cells | Elastic scattering | Infants | Biochemistry | Compaction | Incidence | Proteins | Signal transduction | Diagnosis | Cardiac muscle | Abnormalities | Fetuses | Benign | Recesses | Endothelium | Blood circulation | Morphology | Stem cells | Myocardium | Death | Adults | Notch protein | Cardiovascular diseases | Cardiac arrhythmia | Calcineurin | Risk | Valves | Chin | Transplantation | Defects | Morphogenesis | Children | Cardiology | Ultrasound | Age | Stroke | Health risks | Septum | Ribonucleic acid--RNA | Catheters | Solidification | Magnetic resonance imaging | Ventricle | Methylation | Differentiation | Index Medicus | Abridged Index Medicus
Journal Article