Page last updated: 2024-10-21

mandelic acid and Phenylketonurias

mandelic acid has been researched along with Phenylketonurias in 1 studies

SAMMA: mandelic acid condensation polymer

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 (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (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
ALLEGRANZA, A1
ALDEGHI, E1
CANEVINI, P1
DEVITO, C1

Other Studies

1 other study available for mandelic acid and Phenylketonurias

ArticleYear
[METABOLIC ASPECTS OF PHENYLKETONURIA WITH PARTICULAR ATTENTION TO URINARY ELIMINATION OF SOME PHENOLIC ACIDS].
    Minerva pediatrica, 1964, Sep-15, Volume: 16

    Topics: Adolescent; Attention; Biomedical Research; Child; Humans; Hydroxybenzoates; Indoleacetic Acids; Man

1964