4-hydroxyphenylpyruvic acid has been researched along with Amino Acid Metabolism Disorders, Inborn in 6 studies
4-hydroxyphenylpyruvic acid: RN given refers to parent cpd
4-hydroxyphenylpyruvic acid : A 2-oxo monocarboxylic acid that is pyruvic acid in which one of the methyl hydrogens is substituted by a 4-hydroxyphenyl group.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (66.67) | 18.7374 |
| 1990's | 2 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Machino, H | 1 |
| Miki, Y | 1 |
| Kawatsu, T | 1 |
| Kida, K | 1 |
| Matsuda, H | 1 |
| Furukawa, N | 1 |
| Hayano, T | 1 |
| Sato, N | 1 |
| Inoue, F | 1 |
| Machida, Y | 1 |
| Kinugasa, A | 1 |
| Imashuku, S | 1 |
| Kusunoki, T | 1 |
| Takamatisu, T | 1 |
| Endo, F | 1 |
| Kitano, A | 1 |
| Uehara, I | 1 |
| Nagata, N | 1 |
| Matsuda, I | 1 |
| Shinka, T | 1 |
| Kuhara, T | 1 |
| Matsumoto, I | 1 |
| Ellis, MK | 1 |
| Whitfield, AC | 1 |
| Gowans, LA | 1 |
| Auton, TR | 1 |
| Provan, WM | 1 |
| Lock, EA | 1 |
| Smith, LL | 1 |
| Borden, M | 1 |
| Holm, J | 1 |
| Leslie, J | 1 |
| Sweetman, L | 1 |
| Nyhan, WL | 1 |
| Fleisher, L | 1 |
| Nadler, H | 1 |
| Lewis, D | 1 |
| Scott, CR | 1 |
| Matsuo, M | 1 |
| Saiki, K | 1 |
| Tanabe, J | 1 |
| Nakamura, H | 1 |
| Matsuo, T | 1 |
6 other studies available for 4-hydroxyphenylpyruvic acid and Amino Acid Metabolism Disorders, Inborn
| Article | Year |
|---|---|
Successful dietary control of tyrosinemia II.
Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Corneal Opacity; Female; Humans; Keratins; K | 1983 |
The enzyme defects in hereditary tyrosinaemia type I.
Topics: Amino Acid Metabolism, Inborn Errors; Humans; Hydrolases; Infant, Newborn; Kidney; Liver; Phenylpyru | 1984 |
Four-hydroxyphenylpyruvic acid oxidase deficiency with normal fumarylacetoacetase: a new variant form of hereditary hypertyrosinemia.
Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Adult; Amino Acid Metabolism, Inborn Errors; Consanguinity; Cyt | 1983 |
Inhibition of 4-hydroxyphenylpyruvate dioxygenase by 2-(2-nitro-4-trifluoromethylbenzoyl)-cyclohexane-1,3-dione and 2-(2-chloro-4-methanesulfonylbenzoyl)-cyclohexane-1,3-dione.
Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Amino Acid Metabolism, Inborn Errors; Animals; Cyclohexanones; | 1995 |
Hawkinsinuria in two families.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Cyclohexanecarboxylic Acids; Cy | 1992 |
Citrullinaemia: an infantile form with p-hydroxyphenylpyruvic and p-hydroxyphenyllactic acidurias.
Topics: Amino Acid Metabolism, Inborn Errors; Benzoates; Benzoic Acid; Citrulline; Female; Humans; Infant; P | 1987 |