Last Updated: 09/26/2026
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Found 139 publications
Plasma EV Proteomics Identifies ECM Remodeling and Inflammatory Proteins LUM and C7 as Candidate Biomarkers in FSHD.
Journal: Annals of clinical and translational neurology
Published: April 27, 2026
A randomized, double-blind, placebo-controlled study of losmapimod in patients with facioscapulohumeral muscular dystrophy: Results of the REACH study.
Journal: Journal of neuromuscular diseases
Published: February 06, 2026
Electrical Impedance Myography Detects Disease Progression over 12 to 24 Months in Facioscapulohumeral Muscular Dystrophy.
Journal: Annals of neurology
Published: November 14, 2025
Late-onset facioscapulohumeral muscular dystrophy defines a distinct clinical subgroup.
Journal: Neuromuscular disorders : NMD
Published: November 14, 2025
A pilot study using actigraphy to examine activity performance and its relationship with activity capacity in adults with facioscapulohumeral muscular dystrophy.
Journal: Journal of neuromuscular diseases
Published: October 21, 2025
Concurrent Inclusion Body Myositis and Late Onset Pompe Disease: A Case Report.
Journal: Muscle & nerve
Published: February 03, 2025
Identification of disease-specific extracellular vesicle-associated plasma protein biomarkers for Duchenne Muscular Dystrophy and Facioscapulohumeral Muscular Dystrophy.
Journal: medRxiv : the preprint server for health sciences
Published: December 09, 2024
Strength and functional correlates of reachable workspace in facioscapulohumeral muscular dystrophy.
Strength and functional correlates of reachable workspace in facioscapulohumeral muscular dystrophy.
Journal: Neuromuscular disorders : NMD
Published: October 08, 2024
SMCHD1 maintains heterochromatin, genome compartments and epigenome landscape in human myoblasts.
Journal: Nature communications
Published: October 08, 2024
SMCHD1 maintains heterochromatin and genome compartments in human myoblasts.
Journal: bioRxiv : the preprint server for biology
Published: July 19, 2024
Last Updated: 09/26/2026