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Neuromuscular disorders : NMD, ISSN 0960-8966, 2010, Volume 20, Issue 8, pp. 479 - 492
Summary Cardiac disease is a common clinical manifestation of neuromuscular disorders, particularly of muscular dystrophies. Heart muscle cells as well as... 
Neurology | Treatment | Arrhythmia | Cardiomyopathy | Sudden death | Muscular dystrophy | CONDUCTION-SYSTEM | PROXIMAL MYOTONIC MYOPATHY | CLINICAL SPECTRUM | LINKED DILATED CARDIOMYOPATHY | NEUROSCIENCES | NUCLEAR-MEMBRANE | CLINICAL NEUROLOGY | CAUSE AUTOSOMAL-DOMINANT | LEFT-VENTRICULAR DYSFUNCTION | SUDDEN CARDIAC DEATH | LAMIN A/C GENE | SARCOGLYCAN GENE | Cardiomyopathy, Dilated - pathology | Muscular Dystrophies - therapy | Myofibrils - pathology | Humans | Muscular Dystrophy, Facioscapulohumeral - genetics | Muscular Dystrophies - genetics | Myotonic Dystrophy - pathology | Muscular Dystrophies, Limb-Girdle - genetics | Myotonic Dystrophy - genetics | Genetic Diseases, X-Linked - genetics | Muscular Dystrophies, Limb-Girdle - pathology | Cardiomyopathy, Dilated - genetics | Muscular Dystrophy, Emery-Dreifuss - genetics | Muscular Dystrophies - congenital | Muscular Dystrophy, Emery-Dreifuss - pathology | Muscular Dystrophy, Duchenne - pathology | Myocardium - pathology | Muscular Dystrophies - complications | Muscular Dystrophies - pathology | Muscular Dystrophy, Duchenne - complications | Heart Diseases - etiology | Genetic Diseases, X-Linked - pathology | Muscular Dystrophy, Facioscapulohumeral - pathology | Heterozygote | Muscular Dystrophy, Duchenne - genetics | Heart Diseases - pathology | Heart failure | Cardiology | Genetic aspects
Journal Article
2011, Methods in molecular biology, ISBN 9781617379826, Volume 709., xiii, 382
Book
Journal of cellular and molecular medicine, ISSN 1582-1838, 2018, Volume 22, Issue 4, pp. 2442 - 2448
Journal Article
Circulation (New York, N.Y.), ISSN 1524-4539, 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
Journal Article
Molecular therapy, ISSN 1525-0016, 2017, Volume 25, Issue 5, pp. 1125 - 1131
Duchenne muscular dystrophy (DMD) has been a major target for gene therapy development for nearly 30 years. DMD is among the most common genetic diseases, and... 
gene therapy | muscular dystrophy | dystrophin | microdystrophin | AAV | mdx mice | MOUSE SKELETAL-MUSCLE | MEDICINE, RESEARCH & EXPERIMENTAL | SYSTEMIC DELIVERY | CANINE MODEL | TRANSGENIC MDX MICE | ADENOASSOCIATED VIRUS VECTOR | ADENOVIRAL VECTORS | FULL-LENGTH | INTRAVENOUS-INJECTION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | IN-VIVO | GENETICS & HEREDITY | EXPRESSION | Dependovirus - genetics | Muscular Dystrophy, Animal - genetics | History, 21st Century | Humans | Muscle, Skeletal - metabolism | Muscular Dystrophy, Animal - pathology | Mice, Inbred mdx | Muscular Dystrophy, Animal - metabolism | Protein Domains | Muscular Dystrophy, Animal - therapy | Muscular Dystrophy, Duchenne - therapy | Dystrophin - metabolism | Dependovirus - metabolism | Genetic Vectors - chemistry | History, 20th Century | Genetic Vectors - metabolism | Genetic Therapy - history | Muscular Dystrophy, Duchenne - pathology | Dystrophin - chemistry | Genetic Therapy - trends | Animals | Dystrophin - genetics | Dogs | Mice | Muscular Dystrophy, Duchenne - metabolism | Muscle, Skeletal - pathology | Muscular Dystrophy, Duchenne - genetics | Mutation | Genetic Therapy - methods | Genetic disorders | Clinical trials | FDA approval | Vectors (Biology) | Muscular dystrophy | Design | Proteins | Genetic counseling | Duchenne's muscular dystrophy | Stem cells | Gene therapy | Dystrophin | Review
Journal Article
Nature communications, ISSN 2041-1723, 2017, Volume 8, Issue 1, pp. 16105 - 16105
Journal Article
Journal Article
PloS one, ISSN 1932-6203, 2019, Volume 14, Issue 4, p. e0215590
Considering potential Tempol effects on mdx muscle fibers, in this study we evaluated its effects on relevant dystrophic phenotypic characteristics, such as... 
PREDNISONE | MULTIDISCIPLINARY SCIENCES | MOUSE | MUSCULAR-DYSTROPHY | PERMEABLE RADICAL SCAVENGER | MECHANISMS | DUCHENNE | DIAPHRAGM MUSCLE | DAMAGE | RODENT MODEL | Muscular Dystrophy, Animal - genetics | Muscular Dystrophy, Animal - physiopathology | Humans | Muscle, Skeletal - metabolism | Cyclic N-Oxides - administration & dosage | Muscle Fibers, Skeletal - drug effects | Muscle Fibers, Skeletal - metabolism | Spin Labels | Muscular Dystrophies - genetics | Muscular Dystrophy, Animal - pathology | Cyclic N-Oxides - pharmacology | Muscular Dystrophy, Duchenne - physiopathology | Muscle, Skeletal - drug effects | Mice, Inbred mdx | Diaphragm - metabolism | Muscle Fibers, Skeletal - physiology | Diaphragm - physiopathology | Disease Models, Animal | Mice, Inbred C57BL | Injections, Intraperitoneal | Muscular Dystrophy, Duchenne - pathology | Antioxidants - pharmacology | Muscular Dystrophies - pathology | Phenotype | Animals | Muscle, Skeletal - physiopathology | Antioxidants - administration & dosage | Muscle Strength - drug effects | Muscular Dystrophy, Duchenne - genetics | Muscular Dystrophies - physiopathology | Medical research | Care and treatment | Rats as laboratory animals | Medicine, Experimental | Genetic aspects | Dosage and administration | Research | Health aspects | Muscular dystrophy | Prednisolone | Oxidative stress | Phenotypes | Muscles | Tempol | Inflammatory response | Biochemistry | Biology | Inflammation | Saline solutions | Genotype & phenotype | Angiogenesis | Ischemia | Rodents | Physiology | Mice | Degeneration | Myonecrosis | Muscular strength | Diaphragm
Journal Article
Neurology, ISSN 0028-3878, 10/2014, Volume 83, Issue 18, pp. 1634 - 1644
Journal Article