Page last updated: 2024-10-21

3-methoxytyramine and Amino Acid Metabolism Disorders, Inborn

3-methoxytyramine has been researched along with Amino Acid Metabolism Disorders, Inborn in 1 studies

3-methoxytyramine: RN given refers to parent cpd
3-methoxytyramine : A monomethoxybenzene that is dopamine in which the hydroxy group at position 3 is replaced by a methoxy group. It is a metabolite of the neurotransmitter dopamine and considered a potential biomarker of pheochromocytomas and paragangliomas.

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
Pappan, KL1
Kennedy, AD1
Magoulas, PL1
Hanchard, NA1
Sun, Q1
Elsea, SH1

Other Studies

1 other study available for 3-methoxytyramine and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Clinical Metabolomics to Segregate Aromatic Amino Acid Decarboxylase Deficiency From Drug-Induced Metabolite Elevations.
    Pediatric neurology, 2017, Volume: 75

    Topics: Amino Acid Metabolism, Inborn Errors; Aromatic-L-Amino-Acid Decarboxylases; Carbidopa; Child; Child,

2017