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Lancet, The, ISSN 0140-6736, 2013, Volume 381, Issue 9869, pp. 845 - 860
Journal Article
2011, Methods in molecular biology, ISBN 9781617379826, Volume 709., xiii, 382
Book
2015, Fourth edition., Oxford monographs on medical genetics, ISBN 9780199681488, Volume no. 67., ix, 308 pages
Book
2011, Handbook of clinical neurology, ISBN 0080450318, Volume 3rd ser., v. 101.
Web Resource
2009, 2nd ed., Thefacts series, ISBN 9780199571970, xiii, 106
Book
2008, 3rd ed., The facts, ISBN 0199542163, ix, 149
Book
Neuromuscular Disorders, 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
2013, Neurodegenerative diseases--laboratory and clinical research, ISBN 1626185093
Web Resource
Clinics in Chest Medicine, ISSN 0272-5231, 06/2018, Volume 39, Issue 2, pp. 377 - 389
Journal Article
Neurologic Clinics, ISSN 0733-8619, 2014, Volume 32, Issue 3, pp. 705 - 719
Journal Article
2001, ISBN 0192632914, xii, 316
Book
Journal of Magnetic Resonance Imaging, ISSN 1053-1807, 02/2007, Volume 25, Issue 2, pp. 433 - 440
Interest in muscle MRI has been largely stimulated in the last few years by the recognition of an increasing number of genetic defects in the field of... 
dystrophies | congenital | myopathies | MRI | muscle | Muscle | Myopathies | Dystrophies | Congenital | CONGENITAL MUSCULAR-DYSTROPHY | NEMALINE MYOPATHY | ATROPHY | ABNORMALITIES | INVOLVEMENT | PHENOTYPE | SKELETAL-MUSCLE | ULTRASOUND | RIGID SPINE SYNDROME | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | SARCOGLYCAN | Muscular Atrophy, Spinal - diagnosis | Magnetic Resonance Imaging - trends | History, 21st Century | Humans | Magnetic Resonance Imaging - methods | Myopathies, Structural, Congenital - genetics | Muscular Dystrophies - genetics | Neuromuscular Diseases - pathology | Neuromuscular Diseases - genetics | Muscular Atrophy, Spinal - genetics | Muscular Dystrophies, Limb-Girdle - genetics | Muscular Dystrophy, Emery-Dreifuss - diagnosis | Muscular Dystrophies - diagnosis | Neuromuscular Diseases - diagnosis | Muscular Dystrophies, Limb-Girdle - pathology | Muscular Dystrophy, Emery-Dreifuss - genetics | Muscular Dystrophies, Limb-Girdle - diagnosis | Muscular Dystrophies - congenital | History, 20th Century | Magnetic Resonance Imaging - history | Muscular Dystrophy, Emery-Dreifuss - pathology | Muscular Dystrophy, Duchenne - pathology | Muscular Dystrophies - pathology | Muscular Atrophy, Spinal - pathology | Myopathies, Structural, Congenital - pathology | Myopathies, Structural, Congenital - diagnosis | Muscular Dystrophy, Duchenne - genetics | Muscular Dystrophy, Duchenne - diagnosis
Journal Article
1997, Developments in neurology, ISBN 0444824871, Volume 13., xvii, 440
Book
2006, Neurological disease and therapy, ISBN 0824723252, Volume 79., xxii, 461
Duchenne Muscular Dystrophy (DMD) is one of the most prevalent genetic disorders of childhood and currently stands as an incurable condition. This... 
Treatment | Muscular Dystrophy, Duchenne | Duchenne muscular dystrophy | therapy | Medical Genetics | Neurology | Neuroscience | Muscular Dystrophy, Duchenne - therapy
Book