Page last updated: 2024-10-17

lactic acid and Muscular Dystrophy, Oculopharyngeal

lactic acid has been researched along with Muscular Dystrophy, Oculopharyngeal in 1 studies

Lactic Acid: A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
2-hydroxypropanoic acid : A 2-hydroxy monocarboxylic acid that is propanoic acid in which one of the alpha-hydrogens is replaced by a hydroxy group.

Muscular Dystrophy, Oculopharyngeal: An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in the gene for POLY(A)-BINDING PROTEIN II have been associated with oculopharyngeal muscular dystrophy.

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
Nogueira, C1
Marques, JS1
Nesti, C1
Azevedo, L1
Di Lullo, M1
Meschini, MC1
Orlacchio, A1
Santorelli, FM1
Vilarinho, L1

Other Studies

1 other study available for lactic acid and Muscular Dystrophy, Oculopharyngeal

ArticleYear
Identification of maternal uniparental isodisomy of chromosome 10 in a patient with mitochondrial DNA depletion syndrome.
    Molecular genetics and metabolism, 2013, Volume: 110, Issue:4

    Topics: Brain; Chromosome Aberrations; Chromosomes, Human, Pair 10; DNA, Mitochondrial; Humans; Intestinal P

2013