phenylpyruvic acid has been researched along with Amino Acid Metabolism Disorders, Inborn in 5 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 | 5 (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 |
---|---|
HENNING, U | 1 |
AMMON, R | 1 |
ZETTERSTROEM, R | 1 |
HALVORSEN, S | 1 |
GJESSING, LR | 1 |
HUMBEL, R | 1 |
ALAGILLE, D | 1 |
GENTIL, C | 1 |
5 other studies available for phenylpyruvic acid and Amino Acid Metabolism Disorders, Inborn
Article | Year |
---|---|
[Excretion of p-hydroxyphenylpyruvic acid, phenylpyruvic acid & other alpha-ketone acids in the urine of healthy humans, also a contribution to the problem of tyrosinosis].
Topics: Amino Acid Metabolism, Inborn Errors; Humans; Keto Acids; Ketones; Phenylpyruvic Acids; Tyrosine | 1957 |
TYROSINOSIS.
Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Blood Chemical Analysis; Child; Genetics, Medical; Gl | 1963 |
STUDIES ON TYROSINOSIS: 1, EFFECT OF LOW-TYROSINE AND LOW-PHENYLALANINE DIET.
Topics: Acetates; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Diet; Diet Therapy; Hepatomegaly | 1964 |
[IDENTIFICATION AND DETERMINATION OF P-HYDROXYPHENYLPYRUVIC ACID AND ITS DERIVATIVES IN URINE].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography; Humans; Lactates; Phenylacetates; | 1964 |
[CONGENITAL CIRRHOSIS WITH COMPLEX RENAL TUBULE DISEASE DUE TO AN ANOMALY OF TYROSINE METABOLISM].
Topics: Amino Acid Metabolism, Inborn Errors; Carcinoma, Hepatocellular; Chronic Kidney Disease-Mineral and | 1964 |