Magnetic resonance imaging in facioscapulohumeral muscular dystrophy
Author:
Affiliation:
1. Center for Genetic Muscle Disorders, Kennedy Krieger Institute, 716 North Broadway, Room 411; Baltimore Maryland 21205 USA
2. Department of Neurology; The Johns Hopkins University School of Medicine; Baltimore Maryland USA
Funder
National Institute of Neurological Disorders and Stroke
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology
Reference24 articles.
1. Magnetic resonance imaging patterns of muscle involvement in genetic muscle diseases: a systematic review;Leung;J Neurol,2017
2. A systematic review and meta-analysis on the epidemiology of the muscular dystrophies;Mah;Can J Neurol Sci,2016
3. Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2;Lemmers;Nat Genet,2012
4. Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy;Jones;Clin Epigenetics,2015
5. CRISPR/dCas9-mediated transcriptional inhibition ameliorates the epigenetic dysregulation at D4Z4 and represses DUX4-fl in FSH muscular dystrophy;Himeda;Mol Ther,2016
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2. Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study;Acta Neuropathologica Communications;2023-10-17
3. Five‐year follow‐up study on quantitative muscle magnetic resonance imaging in facioscapulohumeral muscular dystrophy: The link to clinical outcome;Journal of Cachexia, Sarcopenia and Muscle;2023-05-23
4. Facioscapulohumeral muscular dystrophy type 2: an update on the clinical, genetic, and molecular findings;Neuromuscular Disorders;2021-11
5. Profiling Serum Antibodies Against Muscle Antigens in Facioscapulohumeral Muscular Dystrophy Finds No Disease-Specific Autoantibodies;Journal of Neuromuscular Diseases;2021-09-14
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