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MRI as outcome measure in facioscapulohumeral muscular dystrophy: 1-year follow-up of 45 patients.
Andersen G, Dahlqvist JR, Vissing CR, Heje K, Thomsen C, Vissing J. Andersen G, et al. J Neurol. 2017 Mar;264(3):438-447. doi: 10.1007/s00415-016-8361-3. Epub 2016 Dec 20. J Neurol. 2017. PMID: 28000006

Composite absolute fat fraction of all assessed muscles increased by 0.036 (CI 0.026-0.046, P < 0.001), with increases in all measured muscle groups. The clinical severity FSHD score worsened (10%, P < 0.05), muscle strength decreased over the hip (8%), neck (8%), an

Composite absolute fat fraction of all assessed muscles increased by 0.036 (CI 0.026-0.046, P < 0.001), with increases in all measured mu

Facioscapulohumeral muscular dystrophy (FSHD) and multiple sclerosis: a case report.
Iodice R, Ugga L, Aruta F, Iovino A, Ruggiero L. Iodice R, et al. Acta Myol. 2020 Mar 1;39(1):29-31. doi: 10.36185/2532-1900-005. eCollection 2020 Mar. Acta Myol. 2020. PMID: 32607477 Free PMC article.
Facioscapulohumeral muscular dystrophy 1 (FSHD1) is an autosomal dominant neuromuscular disorder, associated with reduction of tandemly arrayed repetitive DNA elements D4Z4 (DRA), at 4q35. ...Herein we report a 33 years old Caucasian with a molecular d
Facioscapulohumeral muscular dystrophy 1 (FSHD1) is an autosomal dominant neuromuscular disorder, associated wit