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Last Updated: 10/31/2025
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Found 1381 publications
Facioscapulohumeral Muscular Dystrophy.
Journal: Continuum (Minneapolis, Minn.)
Published: October 02, 2025
Matrix metalloproteinases are hallmark early biomarkers and therapeutic targets in FSHD.
Journal: JCI insight
Published: September 18, 2025
Transgenic mouse models for investigating human DUX4 expression during development and its roles in FSHD pathophysiology.
Journal: bioRxiv : the preprint server for biology
Published: September 05, 2025
Muscular Dystrophies.
Journal: Advances in experimental medicine and biology
Published: August 29, 2025
Gut Microbiota and Short-Chain Fatty Acid Profiles in Facioscapulohumeral Dystrophy: Associations with Epigenetic Alterations.
Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: August 22, 2025
Diversity challenges and reconciles genetics in facioscapulohumeral muscular dystrophy.
Journal: Journal of human genetics
Published: August 18, 2025
Coats-like Retinopathy Associated With 18p Deletion Syndrome.
Journal: Ophthalmic surgery, lasers & imaging retina
Published: August 11, 2025
Video-based biomechanical analysis captures disease-specific movement signatures of different neuromuscular diseases.
Journal: bioRxiv : the preprint server for biology
Published: August 06, 2025
Disease-specific genetic diagnostic strategies for muscle diseases unresolved by short-read sequencing.
Journal: Journal of human genetics
Published: July 25, 2025
Interleukin-6 as a Key Biomarker in Facioscapulohumeral Dystrophy: Evidence From Longitudinal Analyses.
Journal: Annals of clinical and translational neurology
Published: July 22, 2025
Last Updated: 10/31/2025