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pyruvic acid and Myotonic Dystrophy

pyruvic acid has been researched along with Myotonic Dystrophy in 1 studies

Pyruvic Acid: An intermediate compound in the metabolism of carbohydrates, proteins, and fats. In thiamine deficiency, its oxidation is retarded and it accumulates in the tissues, especially in nervous structures. (From Stedman, 26th ed)
pyruvic acid : A 2-oxo monocarboxylic acid that is the 2-keto derivative of propionic acid. It is a metabolite obtained during glycolysis.

Myotonic Dystrophy: Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
KUHN, E1
WOERNER, W1

Other Studies

1 other study available for pyruvic acid and Myotonic Dystrophy

ArticleYear
[Studies of intermediate metabolism in myotonic dystrophy (lactic acid, pyruvic acid, lactic dehydrogenase and malic acid dehydrogenase)].
    Der Nervenarzt, 1961, Volume: 32

    Topics: Humans; Lactates; Lactic Acid; Malate Dehydrogenase; Malates; Myotonic Dystrophy; Oxidoreductases; P

1961