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pyruvic acid and Brain Diseases, Metabolic, Familial

pyruvic acid has been researched along with Brain Diseases, Metabolic, Familial 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.

Research Excerpts

ExcerptRelevanceReference
"Pyruvate dehydrogenase and pyruvate carboxylase deficiency are the most common disorders in pyruvate metabolism."2.49Disorders of pyruvate metabolism. ( De Meirleir, L, 2013)

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
De Meirleir, L1

Reviews

1 review available for pyruvic acid and Brain Diseases, Metabolic, Familial

ArticleYear
Disorders of pyruvate metabolism.
    Handbook of clinical neurology, 2013, Volume: 113

    Topics: Brain Diseases, Metabolic, Inborn; Humans; Pyruvate Carboxylase; Pyruvate Carboxylase Deficiency Dis

2013