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Journal Article
Annals of Neurology, ISSN 0364-5134, 2000, Volume 48, Issue 2, pp. 170 - 180
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
Journal Article
Stroke, ISSN 0039-2499, 04/2003, Volume 34, Issue 4, pp. 901 - 908
Journal Article
Journal Article
Journal Article
Molecular Medicine Reports, ISSN 1791-2997, 10/2015, Volume 12, Issue 4, pp. 5065 - 5071
The present study aimed to examine and analyze cardiac involvement in two Emery-Dreifuss muscular dystrophy (EDMD) pedigrees caused by the c.1583 C→G mutation... 
lamin A/C | cardiomyopathy | Emery-Dreifuss muscular dystrophy | LMNA | MEDICINE, RESEARCH & EXPERIMENTAL | CONDUCTION-SYSTEM | DOMAIN | NUCLEAR LAMINS | DILATED CARDIOMYOPATHY | FEATURES | MANDIBULOACRAL DYSPLASIA | ONCOLOGY | DISEASE | LAMIN A/C GENE | SPECTRUM | Muscular Dystrophy, Emery-Dreifuss - genetics | Gene Expression | Humans | Muscular Dystrophy, Emery-Dreifuss - pathology | Molecular Sequence Data | Joints - pathology | Muscle, Skeletal - metabolism | Myocardium - pathology | Mutation, Missense | Arrhythmias, Cardiac - physiopathology | Cardiomyopathy, Dilated - physiopathology | Pedigree | Base Sequence | Muscular Dystrophy, Emery-Dreifuss - diagnosis | Myocardium - metabolism | Lamin Type A - genetics | Adult | Female | Heterozygote | Muscular Dystrophy, Emery-Dreifuss - physiopathology | Muscle, Skeletal - pathology | Child | Joints - metabolism | Genetic aspects | Research | Gene mutations | Health aspects | Risk factors | Conduction | Arrhythmia | Cardiomyopathy | Amino acids | Kinases | Muscular dystrophy | Defects | Ultrasonic imaging | Missense mutation | Sinus | C gene | Rodents | Electromyography | Heart diseases | Ultrasound | Deoxyribonucleic acid--DNA | Heart failure | EKG | Immunoglobulins | Cardiac muscle | Histology | Patients | Skeletal muscle | Tachycardia | Disease transmission | Dilated cardiomyopathy | Perfusion | Biopsy | Mutation | Dystrophy | Genetic testing | Adenosine triphosphatase | DNA sequencing | Structure-function relationships | lamin A
Journal Article