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Clinics in Chest Medicine, ISSN 0272-5231, 06/2018, Volume 39, Issue 2, pp. 377 - 389
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 04/2015, Volume 1852, Issue 4, pp. 607 - 614
Facioscapulohumeral muscular dystrophy (FSHD) is characterized by a typical and asymmetric pattern of muscle involvement and disease progression. Two forms of... 
Facioscapulohumeral muscular dystrophy | DNA methylation | Epigenetics | SMCHD1 | Subtelomeric repeat | DUX4 | MENTAL-RETARDATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | FSHD | PHENOTYPE | BIOPHYSICS | GENE | CHROMOSOME 4Q35 | COATS SYNDROME | D4Z4 | POPULATION ANALYSIS | SEQUENCE | Epigenetic inheritance | Development and progression | Muscular dystrophy
Journal Article
Science, ISSN 0036-8075, 9/2010, Volume 329, Issue 5999, pp. 1650 - 1653
Journal Article
Neurologic Clinics, ISSN 0733-8619, 2014, Volume 32, Issue 3, pp. 721 - 728
Facioscapulohumeral muscular dystrophy (FSHD) is a common type of adult muscular dystrophy and is divided into types 1 and 2 based on genetic mutation.... 
Facioscapulohumeral muscular dystrophy | D4Z4 deletion | SMCHD1 mutation | DUX4 | Muscular dystrophy | CONTROLLED-TRIAL | ALBUTEROL | FSHD | NATURAL-HISTORY | DNA REARRANGEMENTS | NEUROSCIENCES | CLINICAL NEUROLOGY | FEATURES | HEARING-LOSS | MUTATION | DOUBLE-BLIND | DELETIONS
Journal Article
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
1993, 1st ed., Molecular and cell biology of human diseases series., ISBN 9780412434402, Volume 3, xvi, 344
Book
CONTINUUM: Lifelong Learning in Neurology, ISSN 1080-2371, 12/2016, Volume 22, Issue 6, Muscle and Neuromuscular Junction Disorders, pp. 1916 - 1931
ABSTRACTPurpose of ReviewThis article describes the clinical characteristics, diagnosis, molecular pathogenesis, and treatment of facioscapulohumeral muscular... 
Muscular Dystrophy, Facioscapulohumeral - diagnosis | Pedigree | Humans | Adolescent | Adult | Male | Muscular Dystrophy, Facioscapulohumeral - genetics | Review
Journal Article