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alanine and Carbohydrate Metabolism, Inborn Error

alanine has been researched along with Carbohydrate Metabolism, Inborn Error in 12 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
" Permanent metabolic acidosis due to lactic acidemia as well as hyperpyruvic acidemia and hyperalaninemia were present."3.66[Pyruvate-dehydrogenase deficiency. Lethal course of the disease during infancy (author's transl)]. ( Becker, K; Berger, R; Bremer, HJ; Przyrembel, H; Walther, B; Wendel, U, 1978)
" They had chronic metabolic acidosis associated with elevated blood levels of lactate, pyruvate, and alanine."3.65Lactic acidosis in three sibs due to defects in both pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase complexes. ( Blass, JP; Hansen, S; Haworth, JC; Perry, TL; Urquhart, N, 1976)

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-199012 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Evans, OB1
Haworth, JC1
Perry, TL1
Blass, JP2
Hansen, S1
Urquhart, N1
Wendel, U1
Przyrembel, H1
Becker, K1
Walther, B1
Berger, R1
Bremer, HJ1
Falk, RE1
Cederbaum, SD1
Gibson, GE1
Kark, RA1
Carrel, RE1
Vidnes, J1
Oyasaeter, S1
Staal, GE1
Ceerdink, RP1
Vlug, AM1
Hamelink, ML1
Bakker, HD1
de Bree, PK1
van Sprang, FJ1
Wadman, SK1
Fernandes, J1
Blom, W1
Launiala, K1
Boisse, J1
Meeuwisse, GW1
Dahlqvist, A1

Reviews

2 reviews available for alanine and Carbohydrate Metabolism, Inborn Error

ArticleYear
Thiamine-responsive lactic acidosis.
    Nutrition reviews, 1974, Volume: 32, Issue:3

    Topics: Acidosis; Alanine; Biotin; Carbohydrate Metabolism, Inborn Errors; Dietary Carbohydrates; Female; Hu

1974
[New etiologic approach to periodic ketoacidosis in children].
    Canadian Medical Association journal, 1971, Aug-07, Volume: 105, Issue:3

    Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Butyrates; Carbohydrate Metabolism, Inborn Errors; Ch

1971

Other Studies

10 other studies available for alanine and Carbohydrate Metabolism, Inborn Error

ArticleYear
Pyruvate decarboxylase deficiency in subacute necrotizing encephalomyelopathy.
    Archives of neurology, 1981, Volume: 38, Issue:8

    Topics: Alanine; Ataxia; Brain; Brain Diseases; Carbohydrate Metabolism, Inborn Errors; Carboxy-Lyases; Huma

1981
Lactic acidosis in three sibs due to defects in both pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase complexes.
    Pediatrics, 1976, Volume: 58, Issue:4

    Topics: Acidosis; Alanine; Carbohydrate Metabolism, Inborn Errors; Electron Transport Complex IV; Female; Gl

1976
[Pyruvate-dehydrogenase deficiency. Lethal course of the disease during infancy (author's transl)].
    Monatsschrift fur Kinderheilkunde, 1978, Volume: 126, Issue:3

    Topics: Acidosis; Alanine; Carbohydrate Metabolism, Inborn Errors; Female; Humans; Infant; Infant, Newborn;

1978
Ketonic diet in the management of pyruvate dehydrogenase deficiency.
    Pediatrics, 1976, Volume: 58, Issue:5

    Topics: Alanine; Carbohydrate Metabolism, Inborn Errors; Child; Citrates; Dietary Carbohydrates; Dietary Fat

1976
Glucagon deficiency causing severe neonatal hypoglycemia in a patient with normal insulin secretion.
    Pediatric research, 1977, Volume: 11, Issue:9 Pt 1

    Topics: Alanine; Amino Acids; Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Glucagon; Gluconeogenes

1977
Defective erythrocyte pyruvate kinase.
    Clinica chimica acta; international journal of clinical chemistry, 1976, Apr-01, Volume: 68, Issue:1

    Topics: Adenosine Triphosphate; Adult; Alanine; Carbohydrate Metabolism, Inborn Errors; Erythrocytes; Fructo

1976
Fructose-1,6-diphosphatase deficiency: another enzyme defect which can present itself with the clinical features of "tyrosinosis".
    Clinica chimica acta; international journal of clinical chemistry, 1974, Aug-30, Volume: 55, Issue:1

    Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carbohydrate Metabolism, Inborn Errors;

1974
The intravenous L-alanine tolerance test as a means for investigating gluconeogenesis.
    Metabolism: clinical and experimental, 1974, Volume: 23, Issue:12

    Topics: Alanine; Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Drug Tolera

1974
The mechanism of diarrhoea in congenital disaccharide malabsorption.
    Acta paediatrica Scandinavica, 1968, Volume: 57, Issue:5

    Topics: Alanine; Carbohydrate Metabolism, Inborn Errors; Diarrhea, Infantile; Disaccharides; Enteral Nutriti

1968
Glucose-galactose malabsorption. A study with biopsy of the small intestinal mucosa.
    Acta paediatrica Scandinavica, 1968, Volume: 57, Issue:4

    Topics: Adolescent; Adult; Alanine; Biological Transport; Biopsy; Carbohydrate Metabolism, Inborn Errors; Ca

1968