prednisolone has been researched along with Phenylketonurias in 2 studies
Prednisolone: A glucocorticoid with the general properties of the corticosteroids. It is the drug of choice for all conditions in which routine systemic corticosteroid therapy is indicated, except adrenal deficiency states.
prednisolone : A glucocorticoid that is prednisone in which the oxo group at position 11 has been reduced to the corresponding beta-hydroxy group. It is a drug metabolite of prednisone.
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 |
---|---|
Exss, R | 1 |
Weber, HP | 1 |
Blau, K | 1 |
Summer, GK | 1 |
Newsome, HC | 1 |
Edwards, CH | 1 |
2 other studies available for prednisolone and Phenylketonurias
Article | Year |
---|---|
[Reticulosarcoma-like skin lesions in phenylketonuria (author's transl)].
Topics: Biopsy; Child; Child, Preschool; Humans; Infant; Lymphoma, Non-Hodgkin; Male; Mercaptopurine; Phenyl | 1975 |
Phenylalanine loading and aromatic acid excretion in normal subjects and heterozygotes for phenylketonuria.
Topics: Adult; Child; Chromatography, Gas; Drug Tolerance; Female; Heterozygote; Humans; Male; Mass Spectrom | 1973 |