4-hydroxyphenylacetic acid has been researched along with Amino Acid Metabolism Disorders, Inborn in 3 studies
4-hydroxyphenylacetic acid : A monocarboxylic acid that is acetic acid in which one of the methyl hydrogens is substituted by a 4-hydroxyphenyl group.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
| Endo, F | 1 |
| Kitano, A | 1 |
| Uehara, I | 1 |
| Nagata, N | 1 |
| Matsuda, I | 1 |
| Shinka, T | 1 |
| Kuhara, T | 1 |
| Matsumoto, I | 1 |
| Faull, KF | 1 |
| Gan, I | 1 |
| Halpern, B | 1 |
| Hammond, J | 1 |
| Im, S | 1 |
| Cotton, RG | 1 |
| Danks, DM | 1 |
| Freeman, R | 1 |
3 other studies available for 4-hydroxyphenylacetic 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 |
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 |
Metabolic studies on two patients with nonhepatic tyrosinemia using deuterated tyrosine loads.
Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Adult; Amino Acid Metabolism, Inborn Errors; Child; Deuterium; | 1977 |