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Circulation, ISSN 0009-7322, 11/2016, Volume 134, Issue Suppl_1 Suppl 1, pp. A15740 - A15740
IntroductionTetralogy of Fallot (TOF) is the most common cyanotic congenital heart defect. Surgical management has resulted in dramatic improvements in... 
Journal Article
Circulation, ISSN 0009-7322, 11/2018, Volume 138, Issue Suppl_1 Suppl 1, pp. A14959 - A14959
IntroductionCardiomyopathy is a leading cause of death in Duchenne muscular dystrophy (DMD). It is characterized by the development of myocardial fibrosis... 
Journal Article
Journal of Cardiac Failure, ISSN 1071-9164, 04/2019, Volume 25, Issue 4, pp. 259 - 267
Cardiomyopathy is the leading cause of death in Duchenne muscular dystrophy (DMD). Standard cardiac biomarkers are poor indicators of DMD cardiovascular... 
fibrosis | cardiomyopathy | Duchenne muscular dystrophy | biomarkers | MORTALITY | PERINDOPRIL | CARDIAC & CARDIOVASCULAR SYSTEMS | BIOMARKER | CARDIAC DYSFUNCTION | NATRIURETIC PEPTIDE | MONITORING DISEASE PROGRESSION | HEART | MUSCLE FUNCTION | VENTRICULAR DYSFUNCTION | SERUM MATRIX-METALLOPROTEINASE-9 | Cardiomyopathy | Heart diseases | Collagen | Cardiac patients
Journal Article
Circulation, ISSN 0009-7322, 11/2016, Volume 134, Issue Suppl_1 Suppl 1, pp. A19945 - A19945
BackgroundCardiomyopathy is the leading cause of death in Duchenne muscular dystrophy (DMD). Biomarkers such as troponin and brain natriuretic peptide do not... 
Journal Article
Cardiology in the Young, ISSN 1047-9511, 03/2019, Volume 29, Issue 3, pp. 290 - 296
Journal Article
Circulation, ISSN 0009-7322, 11/2015, Volume 132, Issue Suppl_3 Suppl 3, pp. A9979 - A9979
BackgroundMarfan syndrome (MFS) is an autosomal dominant disorder that affects the heart, aorta, eyes, skeleton, lungs, and other organs.ObjectiveTo assess... 
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 01/2009, Volume 19, Issue 1, pp. 75 - 75
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 01/2009, Volume 19, Issue 1, p. 75
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2009, Volume 19, Issue 1, pp. 75 - 75
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 01/2009, Volume 19, Issue 1, p. 75
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 11/2014, Volume 371, Issue 22, pp. 2061 - 2071
Journal Article
BMC medical genomics, 04/2017, Volume 10, Issue 1, p. 21
Duchenne muscular dystrophy (DMD) is caused by mutations in the DMD gene, which codes for the dystrophin protein. While progress has been made in defining the... 
Dog Diseases - metabolism | Oligonucleotide Array Sequence Analysis | Dog Diseases - genetics | Muscle, Skeletal - metabolism | Gene Expression Profiling | Organ Specificity | Phenotype | Animals | Myocardium - metabolism | Dogs | Glycolysis | Muscular Dystrophy, Duchenne - metabolism | Muscular Dystrophy, Duchenne - genetics | Mutation
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2008, Volume 19, Issue 1, pp. 75 - 75
Journal Article
Journal of Cardiovascular Magnetic Resonance, ISSN 1532-429X, 01/2013, Volume 15, Issue S1, pp. P149 - P149
  Doc number: P149 
Journal Article
Circulation, ISSN 0009-7322, 11/2018, Volume 138, Issue Suppl_1 Suppl 1, pp. A15207 - A15207
BackgroundDuchenne muscular dystrophy (DMD) leads to progressive cardiomyopathy. Cardiac outcome measures are necessary to evaluate novel cardiac therapeutics.... 
Journal Article
Circulation, ISSN 0009-7322, 08/2017, Volume 136, Issue 13, pp. e200 - e231
For many neuromuscular diseases (NMDs), cardiac disease represents a major cause of morbidity and mortality. The management of cardiac disease in NMDs is made... 
Neuromuscular disease | Pediatrics | Cardiomyopathy | Muscular dystrophy | AHA Scientific Statements | CARDIAC & CARDIOVASCULAR SYSTEMS | CARDIOVASCULAR MAGNETIC-RESONANCE | MECHANICAL CIRCULATORY SUPPORT | neuromuscular disease | CONVERTING ENZYME-INHIBITORS | LUNG TRANSPLANTATION GUIDELINES | LEFT-VENTRICULAR NONCOMPACTION | muscular dystrophy | pediatrics | CHEYNE-STOKES RESPIRATION | LAMIN A/C GENE | PERIPHERAL VASCULAR DISEASE | DUCHENNE MUSCULAR-DYSTROPHY | MYOCARDIAL DELAYED ENHANCEMENT | cardiomyopathy | CARDIOSELECTIVE BETA-BLOCKERS | Myotonic Dystrophy - metabolism | Barth Syndrome - metabolism | Friedreich Ataxia - pathology | Myotonic Dystrophy - diagnosis | United States | Humans | Myopathies, Structural, Congenital - genetics | Neuromuscular Diseases - pathology | Barth Syndrome - pathology | Myotonic Dystrophy - pathology | Muscular Dystrophy, Emery-Dreifuss - diagnosis | Cardiomyopathies - diagnosis | Neuromuscular Diseases - diagnosis | Muscular Dystrophies, Limb-Girdle - pathology | Friedreich Ataxia - metabolism | Muscular Dystrophies, Limb-Girdle - diagnosis | Muscular Diseases - metabolism | Risk Factors | Friedreich Ataxia - diagnosis | Muscular Dystrophy, Emery-Dreifuss - pathology | Cardiomyopathies - pathology | Muscular Dystrophy, Duchenne - pathology | Muscular Diseases - pathology | Barth Syndrome - diagnosis | American Heart Association | Muscular Diseases - diagnosis | Muscular Dystrophy, Emery-Dreifuss - metabolism | Muscular Dystrophies, Limb-Girdle - metabolism | Barth Syndrome - genetics | Neuromuscular Diseases - complications | Myopathies, Structural, Congenital - pathology | Cardiomyopathies - complications | Myopathies, Structural, Congenital - diagnosis | Muscular Dystrophy, Duchenne - metabolism | Myopathies, Structural, Congenital - metabolism | Muscular Dystrophy, Duchenne - diagnosis | Index Medicus | Abridged Index Medicus
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