Page last updated: 2024-10-22

acetovanillone and Phenylketonurias

acetovanillone has been researched along with Phenylketonurias in 1 studies

apocynin : An aromatic ketone that is 1-phenylethanone substituted by a hydroxy group at position 4 and a methoxy group at position 3.

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-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lu, L1
Gu, X1
Li, D1
Liang, L1
Zhao, Z1
Gao, J1

Other Studies

1 other study available for acetovanillone and Phenylketonurias

ArticleYear
Mechanisms regulating superoxide generation in experimental models of phenylketonuria: an essential role of NADPH oxidase.
    Molecular genetics and metabolism, 2011, Volume: 104, Issue:3

    Topics: Acetophenones; Animals; Blotting, Western; Cells, Cultured; Cerebral Cortex; Chromatography, Liquid;

2011