formaldehyde has been researched along with Phenylketonurias in 1 studies
paraform: polymerized formaldehyde; RN given refers to parent cpd; used in root canal therapy
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 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Nasser, A | 1 |
| Bjerrum, OJ | 1 |
| Heegaard, AM | 1 |
| Møller, AT | 1 |
| Larsen, M | 1 |
| Dalbøge, LS | 1 |
| Dupont, E | 1 |
| Jensen, TS | 1 |
| Møller, LB | 1 |
1 other study available for formaldehyde and Phenylketonurias
| Article | Year |
|---|---|
Impaired behavioural pain responses in hph-1 mice with inherited deficiency in GTP cyclohydrolase 1 in models of inflammatory pain.
Topics: Animals; Behavior, Animal; Biopterins; Biosynthetic Pathways; Capsaicin; Chromatography, High Pressu | 2013 |