Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for “double trouble” overlapping syndromes [PDF]
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Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations [PDF]
Kohei Hamanaka +8 more
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Skeletal muscle regeneration in facioscapulohumeral muscular dystrophy is correlated with pathological severity [PDF]
Christopher R. S. Banerji +3 more
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Visual Diagnosis of Facioscapulohumeral Muscular Dystrophy (FSHD). [PDF]
Erdmann H, Abicht A, Becker K.
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Clinical practice considerations in facioscapulohumeral muscular dystrophy Sydney, Australia, 21 September 2015 [PDF]
Rabi Tawil +17 more
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Proteomics of Muscle Microdialysates Identifies Potential Circulating Biomarkers in Facioscapulohumeral Muscular Dystrophy [PDF]
Victor Corasolla Carregari +6 more
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DUX4 at 25: how it emerged from "junk DNA" to become the cause of facioscapulohumeral muscular dystrophy. [PDF]
Belayew A, Rosa AL, Zammit PS.
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Treatment of Facioscapulohumeral Muscular Dystrophy (FSHD): A Systematic Review. [PDF]
Aguirre AS +8 more
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A Deoxyribonucleic Acid Decoy Trapping DUX4 for the Treatment of Facioscapulohumeral Muscular Dystrophy [PDF]
Virginie Mariot +5 more
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