isoniazid has been researched along with Phenylketonurias in 2 studies
Hydra: A genus of freshwater polyps in the family Hydridae, order Hydroida, class HYDROZOA. They are of special interest because of their complex organization and because their adult organization corresponds roughly to the gastrula of higher animals.
hydrazide : Compounds derived from oxoacids RkE(=O)l(OH)m (l =/= 0) by replacing -OH by -NRNR2 (R groups are commonly H). (IUPAC).
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 | 2 (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 |
|---|---|
| Feist, D | 1 |
| Robbner, JA | 1 |
| Eberle, E | 1 |
| Gryglewski, R | 1 |
1 review available for isoniazid and Phenylketonurias
| Article | Year |
|---|---|
[Medical pharmacogenetics. I. Methods applied in pharmacogenetic studies].
Topics: Catecholamines; Genetics, Medical; Humans; Isoniazid; Methemoglobinemia; Methods; Pharmacogenetics; | 1967 |
1 other study available for isoniazid and Phenylketonurias
| Article | Year |
|---|---|
[Severe drug-induced jaundice due to isonicotinic acid hydrazine (INH) in a phenylketonuric boy. Clinical course and electron microscope findings in the liver (author's transl)].
Topics: Biopsy; Chemical and Drug Induced Liver Injury; Child, Preschool; Endoplasmic Reticulum; Glycogen; H | 1973 |