phenylpyruvic acid has been researched along with Diseases, Metabolic in 4 studies
phenylpyruvic acid: RN given refers to parent cpd
phenylpyruvate : A 2-oxo monocarboxylic acid anion resulting from deprotonation of the carboxy group of either keto- or enol-phenylpyruvic acid.
keto-phenylpyruvic acid : A 2-oxo monocarboxylic acid that is 3-phenylpropanoic acid substituted by an oxo group at position 2. It is an intermediate metabolite in the phenylalanine pathway.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (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 |
|---|---|
| ZETTERSTROEM, R | 1 |
| FRITZELL, S | 1 |
| JAGENBURG, OR | 1 |
| SCHNUERER, LB | 1 |
| WOOLLEY, DW | 1 |
| VANDERHOEVEN, T | 1 |
| KVIATKOVSKAIA, AN | 1 |
| KAINOVA, AS | 1 |
| MIKHAILOVA, IN | 1 |
4 other studies available for phenylpyruvic acid and Diseases, Metabolic
| Article | Year |
|---|---|
TYROSINOSIS.
Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Blood Chemical Analysis; Child; Genetics, Medical; Gl | 1963 |
FAMILIAL CIRRHOSIS OF THE LIVER, RENAL TUBULAR DEFECTS WITH RICKETS AND IMPAIRED TYROSINE METABOLISM.
Topics: Child; Chronic Kidney Disease-Mineral and Bone Disorder; Genetic Diseases, Inborn; Genetics; Humans; | 1964 |
SEROTONIN DEFICIENCY IN INFANCY AS ONE CAUSE OF A MENTAL DEFECT IN PHENYLKETONURIA.
Topics: Animals; Animals, Newborn; Behavior; Catecholamines; Chlorpromazine; Genetics; Learning; Metabolic D | 1964 |
[TYROSINE METABOLISM DISORDERS IN PATIENTS WITH COLLAGEN DISEASES. II. 2,5-DIHYDROXYPHENYLPYRUVIC ACID AND ITS CLINICAL SIGNIFICANCE IN COLLAGEN DISEASES].
Topics: Collagen Diseases; Humans; Metabolic Diseases; Phenylpyruvic Acids; Tyrosine; Urine | 1964 |