Page last updated: 2024-10-23

berberine and Muscular Dystrophy, Facioscapulohumeral

berberine has been researched along with Muscular Dystrophy, Facioscapulohumeral in 1 studies

Muscular Dystrophy, Facioscapulohumeral: An autosomal dominant degenerative muscle disease characterized by slowly progressive weakness of the muscles of the face, upper-arm, and shoulder girdle. The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation. This tends to be followed by facial weakness, primarily involving the orbicularis oris and orbicularis oculi muscles. (Neuromuscul Disord 1997;7(1):55-62; Adams et al., Principles of Neurology, 6th ed, p1420)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
Ciszewski, L1
Lu-Nguyen, N1
Slater, A1
Brennan, A1
Williams, HEL1
Dickson, G1
Searle, MS1
Popplewell, L1

Other Studies

1 other study available for berberine and Muscular Dystrophy, Facioscapulohumeral

ArticleYear
G-quadruplex ligands mediate downregulation of DUX4 expression.
    Nucleic acids research, 2020, 05-07, Volume: 48, Issue:8

    Topics: Animals; Berberine; Cell Fusion; Cell Line, Tumor; Clone Cells; Down-Regulation; Enhancer Elements,

2020