pyruvic acid has been researched along with Abnormalities, Congenital, Nervous System 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.
Excerpt | Relevance | Reference |
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"Although confirmation of PDH deficiency depends on specialized biochemical analyses, neonatal MRI plays a role in evaluating the pattern and extent of brain damage, and potentially in early diagnosis and clinical decision making." | 1.35 | Neonatal pyruvate dehydrogenase deficiency due to a R302H mutation in the PDHA1 gene: MRI findings. ( Cruz, R; Leijser, LM; Magalhães, Z; Ribeiro, M; Rocha, JF; Soares-Fernandes, JP; Teixeira-Gomes, R, 2008) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Soares-Fernandes, JP | 1 |
Teixeira-Gomes, R | 1 |
Cruz, R | 1 |
Ribeiro, M | 1 |
Magalhães, Z | 1 |
Rocha, JF | 1 |
Leijser, LM | 1 |
1 other study available for pyruvic acid and Abnormalities, Congenital, Nervous System
Article | Year |
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Neonatal pyruvate dehydrogenase deficiency due to a R302H mutation in the PDHA1 gene: MRI findings.
Topics: Brain; Diagnosis, Differential; Diffusion Magnetic Resonance Imaging; Humans; Infant, Newborn; Lacti | 2008 |