pyruvic acid has been researched along with Glycogenosis in 5 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 |
|---|---|---|
| "Polysaccharide storage myopathy (PSSM) is a distinct cause of exertional rhabdomyolysis in Quarter Horses that results in glycogen and abnormal polysaccharide accumulation." | 3.70 | Skeletal muscle metabolic response to exercise in horses with 'tying-up' due to polysaccharide storage myopathy. ( Billstrom, JA; Hower-Moritz, MA; Macleay, JM; Mickelson, JR; Valberg, SJ, 1999) |
| "The ketosis was reversed by glucagon administration." | 1.27 | Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiency. ( Brown, BI; Burke, BA; Tuchman, M; Ulstrom, RA, 1986) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (60.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Serrano-Lorenzo, P | 1 |
| Rabasa, M | 1 |
| Esteban, J | 1 |
| Hidalgo Mayoral, I | 1 |
| Domínguez-González, C | 1 |
| Blanco-Echevarría, A | 1 |
| Garrido-Moraga, R | 1 |
| Lucia, A | 1 |
| Blázquez, A | 1 |
| Rubio, JC | 1 |
| Palma-Milla, C | 1 |
| Arenas, J | 1 |
| Martín, MA | 1 |
| OEI, TL | 1 |
| Valberg, SJ | 1 |
| Macleay, JM | 1 |
| Billstrom, JA | 1 |
| Hower-Moritz, MA | 1 |
| Mickelson, JR | 1 |
| Tuchman, M | 1 |
| Brown, BI | 1 |
| Burke, BA | 1 |
| Ulstrom, RA | 1 |
| van Riet, W | 1 |
| de Meirsman, J | 1 |
| de Saedeleer, J | 1 |
| Dom, R | 1 |
| Carton, H | 1 |
| van den Heede, J | 1 |
| Bulcke, JA | 1 |
5 other studies available for pyruvic acid and Glycogenosis
| Article | Year |
|---|---|
Clinical, Biochemical, and Molecular Characterization of Two Families with Novel Mutations in the
Topics: Codon, Nonsense; Dermatitis; Female; Glycogen Storage Disease; Humans; Isoenzymes; Lactate Dehydroge | 2022 |
Hexose monophosphate, pyruvate and lactate in the peripheral blood in glycogen-storage disease type I.
Topics: Glycogen; Glycogen Storage Disease; Hexosephosphates; Hexoses; Humans; Lactates; Lactic Acid; Pyruva | 1962 |
Skeletal muscle metabolic response to exercise in horses with 'tying-up' due to polysaccharide storage myopathy.
Topics: Adenosine Triphosphate; Animals; Female; Glucose-6-Phosphate; Glycogen; Glycogen Storage Disease; He | 1999 |
Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiency.
Topics: 3-Hydroxybutyric Acid; Alanine; Blood Glucose; Child, Preschool; Glycogen Storage Disease; Histocyto | 1986 |
Early onset myophosphorylase deficiency (Mc Ardle's disease) with absence of myophosphorylase protein on SDS electrophoresis. The role of the ischemic forearm test.
Topics: Adult; Biopsy; Electromyography; Electrophoresis, Polyacrylamide Gel; Exercise Test; Female; Forearm | 1985 |