Compounds > alpha-methyl-beta-hydroxybutyrate

Page last updated: 2024-09-04

alpha-methyl-beta-hydroxybutyrate and Acidosis

alpha-methyl-beta-hydroxybutyrate has been researched along with Acidosis in 6 studies

Research

Studies (6)

Timeframe	Studies, this research(%)	All Research%
pre-1990	4 (66.67)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (16.67)	29.6817
2010's	1 (16.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bancel, LP; Dessein, AF; Germain, N; Guemann, AS; Joncquel Chevalier Curt, M	1
da C Ferreira, G; Dalcin, KB; de Assis, DR; Filho, CS; Latini, A; Leipnitz, G; Maria, RC; Perry, ML; Ribeiro, CA; Rosa, RB; Schuck, PF; Wajner, M; Wannmacher, CM; Wyse, AT	1
Bennett, MJ; Littlewood, JM; MacDonald, A; Pollitt, RJ; Thompson, J	1
Condado, I; DelValle, JA; Garcia, MJ; Jiménez, A; López, O; Merinero, B; Solaguren, R; Ugarte, M	1
Middleton, B; Oorthuys, JW; Schutgens, RB; Tegelaers, WH; vd Blij, JF; Veder, HA; Vulsma, T	1
Leonard, JV; Middleton, B; Seakins, JW	1

Other Studies

6 other study(ies) available for alpha-methyl-beta-hydroxybutyrate and Acidosis

Article	Year
Abnormal Ketone Bodies in a 22-Month-Old Boy Presenting with Recurrent Vomiting and Metabolic Acidosis. Clinical chemistry, 2019, Volume: 65, Issue:11 Topics: Acetoacetates; Acetyl-CoA C-Acyltransferase; Acidosis; Amino Acid Metabolism, Inborn Errors; Glycine; Humans; Hydroxybutyrates; Infant; Ketone Bodies; Male; Vomiting	2019
Inhibition of energy metabolism by 2-methylacetoacetate and 2-methyl-3-hydroxybutyrate in cerebral cortex of developing rats. Journal of inherited metabolic disease, 2005, Volume: 28, Issue:4 Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acetates; Acetoacetates; Acetyl-CoA C-Acyltransferase; Acidosis; Alcohol Oxidoreductases; Animals; Brain; Carbon Dioxide; Cerebral Cortex; Citrates; Creatine Kinase; Dose-Response Relationship, Drug; Electron Transport; Energy Metabolism; Glucose; Glutathione; Glycine; Hydroxybutyrates; In Vitro Techniques; Intellectual Disability; Lactic Acid; NG-Nitroarginine Methyl Ester; Oxygen; Rats; Rats, Wistar; Time Factors	2005
A case of beta-ketothiolase deficiency. Journal of inherited metabolic disease, 1983, Volume: 6, Issue:4 Topics: Acetyl-CoA C-Acyltransferase; Acidosis; Acyltransferases; Dietary Proteins; Female; Glycine; Humans; Hydroxybutyrates; Infant	1983
Late onset type of propionic acidaemia: case report and biochemical studies. Journal of inherited metabolic disease, 1981, Volume: 4, Issue:2 Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Carbon-Carbon Ligases; Female; Glycine; Humans; Hydroxybutyrates; Infant; Ketosis; Ligases; Propionates	1981
Beta-ketothiolase deficiency in a family confirmed by in vitro enzymatic assays in fibroblasts. European journal of pediatrics, 1982, Volume: 139, Issue:1 Topics: Acetyl-CoA C-Acyltransferase; Acidosis; Acyltransferases; Adult; Child; Fibroblasts; Glycine; Humans; Hydroxybutyrates; Male; Metabolism, Inborn Errors	1982
Acetoacetyl CoA thiolase deficiency presenting as ketotic hypoglycemia. Pediatric research, 1987, Volume: 21, Issue:2 Topics: Acetoacetates; Acetyl-CoA C-Acetyltransferase; Acetyltransferases; Acidosis; Female; Glycine; Humans; Hydroxybutyrates; Hypoglycemia; Infant; Ketosis	1987