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prednisolone and Phenylketonurias

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).

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19902 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Exss, R1
Weber, HP1
Blau, K1
Summer, GK1
Newsome, HC1
Edwards, CH1

Other Studies

2 other studies available for prednisolone and Phenylketonurias

ArticleYear
[Reticulosarcoma-like skin lesions in phenylketonuria (author's transl)].
    Monatsschrift fur Kinderheilkunde, 1975, Volume: 123, Issue:3

    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.
    Clinica chimica acta; international journal of clinical chemistry, 1973, May-18, Volume: 45, Issue:3

    Topics: Adult; Child; Chromatography, Gas; Drug Tolerance; Female; Heterozygote; Humans; Male; Mass Spectrom

1973