phenylpyruvic acid has been researched along with Liver Cirrhosis 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.
Liver Cirrhosis: Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules.
| 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 |
|---|---|
| AMMON, R | 1 |
| HENNING, U | 1 |
| FRITZELL, S | 1 |
| JAGENBURG, OR | 1 |
| SCHNUERER, LB | 1 |
| AKISAWA, J | 1 |
| ALAGILLE, D | 1 |
| GENTIL, C | 1 |
4 other studies available for phenylpyruvic acid and Liver Cirrhosis
| Article | Year |
|---|---|
[Appearance of p-hydroxyphenylpyruvic acid and other alpha-ketone acids in the urine of healthy rabbits and with liver cirrhosis].
Topics: Animals; Health; Humans; Keto Acids; Ketones; Liver Cirrhosis; Phenylpyruvic Acids; Rabbits | 1957 |
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 |
[CLINICAL STUDIES ON THE INTERMEDIARY METABOLISM OF TYROSINE. 1. URINARY EXCRETION OF INTERMEDIARY METABOLITES OF TYROSINE IN HEALTHY INDIVIDUALS AND PATIENTS WITH LIVER DISORDERS].
Topics: Biomedical Research; Hepatitis; Hepatitis A; Humans; Lactates; Liver Cirrhosis; Liver Diseases; Live | 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 |