thiamine has been researched along with Ataxia with Lactic Acidosis 2 in 5 studies
thiamine(1+) : A primary alcohol that is 1,3-thiazol-3-ium substituted by (4-amino-2-methylpyrimidin-5-yl)methyl, methyl and 2-hydroxyethyl groups at positions 3, 4 and 5, respectively.
Excerpt | Relevance | Reference |
---|---|---|
" This infant was found to have lactic acidosis, low cerebrospinal fluid glucose, hyperalaninemia, and increased levels of urine lactate, pyruvate and alanine." | 7.65 | Hyperalaninemia hyperpyruvicemia and lactic acidosis due to pyruvate carboxylase deficiency of the liver; treatment with thiamine and lipoic acid. ( Komiya, K; Maesaka, H; Misugi, K; Tada, K, 1976) |
" This infant was found to have lactic acidosis, low cerebrospinal fluid glucose, hyperalaninemia, and increased levels of urine lactate, pyruvate and alanine." | 3.65 | Hyperalaninemia hyperpyruvicemia and lactic acidosis due to pyruvate carboxylase deficiency of the liver; treatment with thiamine and lipoic acid. ( Komiya, K; Maesaka, H; Misugi, K; Tada, K, 1976) |
"Treatment with aspartic acid and thiamine over a period of seven years resulted in biochemical improvement and a stable neurological condition." | 1.26 | A patient with pyruvate carboxylase deficiency in the liver: treatment with aspartic acid and thiamine. ( Baal, MG; Gabreëls, FJ; Gijsbers, TH; Hommes, FA; Kok, JC; Lamers, KJ; Renier, WO, 1981) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (80.00) | 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 | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bartlett, K | 1 |
Goodyer, PR | 1 |
Lancaster, GA | 1 |
Baal, MG | 1 |
Gabreëls, FJ | 1 |
Renier, WO | 1 |
Hommes, FA | 1 |
Gijsbers, TH | 1 |
Lamers, KJ | 1 |
Kok, JC | 1 |
Robinson, BH | 1 |
MacKay, N | 1 |
Chun, K | 1 |
Ling, M | 1 |
Maesaka, H | 1 |
Komiya, K | 1 |
Misugi, K | 1 |
Tada, K | 1 |
2 reviews available for thiamine and Ataxia with Lactic Acidosis 2
Article | Year |
---|---|
Vitamin-responsive inborn errors of metabolism.
Topics: Acetyl-CoA Carboxylase; Acidosis; Amino Acid Metabolism, Inborn Errors; Animals; Biotin; Folic Acid; | 1983 |
Disorders of pyruvate carboxylase and the pyruvate dehydrogenase complex.
Topics: Amino Acid Sequence; Female; Humans; Male; Molecular Sequence Data; Mutation; Pyruvate Carboxylase; | 1996 |
3 other studies available for thiamine and Ataxia with Lactic Acidosis 2
Article | Year |
---|---|
Inherited lactic acidosis: correction of the defect in cultured fibroblasts.
Topics: Acidosis; Cells, Cultured; Electron Transport; Female; Fibroblasts; Humans; Infant, Newborn; Lactate | 1984 |
A patient with pyruvate carboxylase deficiency in the liver: treatment with aspartic acid and thiamine.
Topics: Aspartic Acid; Child; Female; Humans; Lactates; Lactic Acid; Liver; Psychological Tests; Pyruvate Ca | 1981 |
Hyperalaninemia hyperpyruvicemia and lactic acidosis due to pyruvate carboxylase deficiency of the liver; treatment with thiamine and lipoic acid.
Topics: Acidosis; Alanine; Female; Glucose; Humans; Infant; Intellectual Disability; Lactates; Liver; Metabo | 1976 |