indole has been researched along with Phenylketonurias in 5 studies
Phenylketonurias: A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952).
| 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 |
|---|---|
| ARMSTRONG, MD | 1 |
| ROBINSON, KS | 1 |
| SCHREIER, K | 1 |
| FLAIG, H | 1 |
| HSIA, DY | 1 |
| HUANG, I | 1 |
| FISCHL, J | 1 |
| RABIAH, S | 1 |
| PARE, CM | 1 |
| SANDLER, M | 1 |
| STACEY, RS | 1 |
5 other studies available for indole and Phenylketonurias
| Article | Year |
|---|---|
On the excretion of indole derivatives in phenylketonuria.
Topics: Biological Transport; Humans; Indoles; Intellectual Disability; Phenylketonurias | 1954 |
[Urinary excretion of indole-pyroracemic acid in normal conditions and in Fölling's disease].
Topics: Body Fluids; Humans; Indoles; Intellectual Disability; Phenylketonurias; Pyruvates | 1956 |
The metabolism of indole-compounds in phenvlketonuria.
Topics: Biochemical Phenomena; Indoles; Phenylalanine; Phenylketonurias | 1961 |
DETERMINATION OF FREE AND TOTAL INDOLE-3-ACETIC ACID AND OF THE INDOLE INDEX.
Topics: Friedreich Ataxia; Humans; Indoleacetic Acids; Indoles; Intestines; Kynurenine; Metabolism; Myotonia | 1964 |
The relationship between decreased 5-hydroxyindole metabolism and mental defect in phenylketonuria.
Topics: Humans; Indoles; Muscular Diseases; Phenylketonurias | 1959 |