2-methylacetoacetic acid has been researched along with alpha-methyl-beta-hydroxybutyrate in 6 studies
Studies (2-methylacetoacetic acid) | Trials (2-methylacetoacetic acid) | Recent Studies (post-2010) (2-methylacetoacetic acid) | Studies (alpha-methyl-beta-hydroxybutyrate) | Trials (alpha-methyl-beta-hydroxybutyrate) | Recent Studies (post-2010) (alpha-methyl-beta-hydroxybutyrate) |
---|---|---|---|---|---|
9 | 0 | 2 | 23 | 0 | 5 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (33.33) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (33.33) | 29.6817 |
2010's | 2 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Leonard, JV; Middleton, B; Seakins, JW | 1 |
Bartlett, K; Middleton, B | 1 |
Fukao, T; Hazama, A; Kohno, Y; Kondo, M; Kondo, N; Kubo, T; Matsuo, N; Sakura, N; Shigematsu, Y; Yamaga, H; Yamaguchi, S; Zhang, GX | 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 |
Amaral, AU; Dutra-Filho, CS; Fernandes, CG; Leipnitz, G; Seminotti, B; Wajner, M | 1 |
Bancel, LP; Dessein, AF; Germain, N; Guemann, AS; Joncquel Chevalier Curt, M | 1 |
6 other study(ies) available for 2-methylacetoacetic acid and alpha-methyl-beta-hydroxybutyrate
Article | Year |
---|---|
Acetoacetyl CoA thiolase deficiency presenting as ketotic hypoglycemia.
Topics: Acetoacetates; Acetyl-CoA C-Acetyltransferase; Acetyltransferases; Acidosis; Female; Glycine; Humans; Hydroxybutyrates; Hypoglycemia; Infant; Ketosis | 1987 |
The synthesis and characterisation of 2-methylacetoacetyl coenzyme A and its use in the identification of the site of the defect in 2-methylacetoacetic and 2-methyl-3-hydroxybutyric aciduria.
Topics: Acetoacetates; Acetyl-CoA C-Acetyltransferase; Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Cells, Cultured; Child, Preschool; Fibroblasts; Humans; Hydroxybutyrates; Isoleucine | 1983 |
The mitochondrial acetoacetyl-CoA thiolase (T2) deficiency in Japanese patients: urinary organic acid and blood acylcarnitine profiles under stable conditions have subtle abnormalities in T2-deficient patients with some residual T2 activity.
Topics: Acetoacetates; Acetyl-CoA C-Acetyltransferase; Amino Acid Metabolism, Inborn Errors; Carnitine; Humans; Hydroxybutyrates; Infant; Isoleucine; Ketone Bodies; Male; Mitochondria; Mutation | 2003 |
Inhibition of energy metabolism by 2-methylacetoacetate and 2-methyl-3-hydroxybutyrate in cerebral cortex of developing rats.
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 |
Evidence that 2-methylacetoacetate induces oxidative stress in rat brain.
Topics: Acetoacetates; Animals; Brain; Brain Diseases, Metabolic; Cerebral Cortex; Hydroxybutyrates; Lipid Peroxidation; Oxidative Stress; Rats; Rats, Wistar | 2010 |
Abnormal Ketone Bodies in a 22-Month-Old Boy Presenting with Recurrent Vomiting and Metabolic Acidosis.
Topics: Acetoacetates; Acetyl-CoA C-Acyltransferase; Acidosis; Amino Acid Metabolism, Inborn Errors; Glycine; Humans; Hydroxybutyrates; Infant; Ketone Bodies; Male; Vomiting | 2019 |