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alanine and Ataxia with Lactic Acidosis 2

alanine has been researched along with Ataxia with Lactic Acidosis 2 in 4 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

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)
"To report the clinical history and laboratory evaluation of a patient presenting with lactic acidosis secondary to pyruvate carboxylase deficiency."3.69Prolonged survival in pyruvate carboxylase deficiency: lack of correlation with enzyme activity in cultured fibroblasts. ( Depalma, L; Nayar, R; Rifai, N; Stern, HJ, 1995)
" 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)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19903 (75.00)18.7374
1990's1 (25.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Stern, HJ1
Nayar, R1
Depalma, L1
Rifai, N1
Tada, K2
Takada, G1
Omura, K1
Itokawa, Y1
Maesaka, H1
Komiya, K1
Misugi, K1
Saudubray, JM1
Marsac, C1
Cathelineau, CL1
Besson Leaud, M1
Leroux, JP1

Other Studies

4 other studies available for alanine and Ataxia with Lactic Acidosis 2

ArticleYear
Prolonged survival in pyruvate carboxylase deficiency: lack of correlation with enzyme activity in cultured fibroblasts.
    Clinical biochemistry, 1995, Volume: 28, Issue:1

    Topics: Acidosis, Lactic; Adult; Alanine; Cells, Cultured; Child; Child, Preschool; Female; Fibroblasts; Hum

1995
Congenital lactic acidosis due to pyruvate carboxylase deficiency: absence of an inhibitor of TPP-ATP phosphoryl transferase.
    European journal of pediatrics, 1978, Jan-17, Volume: 127, Issue:2

    Topics: Acidosis; Alanine; Brain Stem; Child, Preschool; Encephalomalacia; Female; Humans; Infant; Intellect

1978
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
Neonatal congenital lactic acidosis with pyruvate carboxylase deficiency in two siblings.
    Acta paediatrica Scandinavica, 1976, Volume: 65, Issue:6

    Topics: Acetoacetates; Acidosis; Alanine; Female; Humans; Hydroxybutyrates; Infant, Newborn; Infant, Newborn

1976