Page last updated: 2024-10-26

erythrosine and Muscular Dystrophy, Duchenne

erythrosine has been researched along with Muscular Dystrophy, Duchenne in 1 studies

Fluoresceins: A family of spiro(isobenzofuran-1(3H),9'-(9H)xanthen)-3-one derivatives. These are used as dyes, as indicators for various metals, and as fluorescent labels in immunoassays.

Muscular Dystrophy, Duchenne: An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415)

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's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chen, CA1
Chang, MY1
Chang, TM1
Jong, YJ1
Wu, SM1

Other Studies

1 other study available for erythrosine and Muscular Dystrophy, Duchenne

ArticleYear
Capillary electrophoresis for analysis of deletion and duplication in exon 44-55 of Duchenne muscular dystrophy gene.
    Electrophoresis, 2013, Volume: 34, Issue:17

    Topics: Case-Control Studies; DNA Mutational Analysis; Dystrophin; Electrophoresis, Capillary; Exons; Fluore

2013