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thiamine and Ataxia with Lactic Acidosis 2

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.

Research Excerpts

ExcerptRelevanceReference
" This infant was found to have lactic acidosis, low cerebrospinal fluid glucose, hyperalaninemia, and increased levels of urine lactate, pyruvate and alanine."7.65Hyperalaninemia 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."3.65Hyperalaninemia 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."1.26A 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)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19904 (80.00)18.7374
1990's1 (20.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bartlett, K1
Goodyer, PR1
Lancaster, GA1
Baal, MG1
Gabreëls, FJ1
Renier, WO1
Hommes, FA1
Gijsbers, TH1
Lamers, KJ1
Kok, JC1
Robinson, BH1
MacKay, N1
Chun, K1
Ling, M1
Maesaka, H1
Komiya, K1
Misugi, K1
Tada, K1

Reviews

2 reviews available for thiamine and Ataxia with Lactic Acidosis 2

ArticleYear
Vitamin-responsive inborn errors of metabolism.
    Advances in clinical chemistry, 1983, Volume: 23

    Topics: Acetyl-CoA Carboxylase; Acidosis; Amino Acid Metabolism, Inborn Errors; Animals; Biotin; Folic Acid;

1983
Disorders of pyruvate carboxylase and the pyruvate dehydrogenase complex.
    Journal of inherited metabolic disease, 1996, Volume: 19, Issue:4

    Topics: Amino Acid Sequence; Female; Humans; Male; Molecular Sequence Data; Mutation; Pyruvate Carboxylase;

1996

Other Studies

3 other studies available for thiamine and Ataxia with Lactic Acidosis 2

ArticleYear
Inherited lactic acidosis: correction of the defect in cultured fibroblasts.
    Pediatric research, 1984, Volume: 18, Issue:11

    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.
    Developmental medicine and child neurology, 1981, Volume: 23, Issue:4

    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.
    European journal of pediatrics, 1976, May-04, Volume: 122, Issue:2

    Topics: Acidosis; Alanine; Female; Glucose; Humans; Infant; Intellectual Disability; Lactates; Liver; Metabo

1976