Page last updated: 2024-10-21

3-methoxytyrosine and Metabolic Diseases

3-methoxytyrosine has been researched along with Metabolic Diseases in 1 studies

Metabolic Diseases: Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed)

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
Pons, R1
Serrano, M1
Ormazabal, A1
Toma, C1
Garcia-Cazorla, A1
Area, E1
Ribasés, M1
Kanavakis, E1
Drakaki, K1
Giannakopoulos, A1
Orfanou, I1
Youroukos, S1
Cormand, B1
Artuch, R1

Other Studies

1 other study available for 3-methoxytyrosine and Metabolic Diseases

ArticleYear
Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation.
    Movement disorders : official journal of the Movement Disorder Society, 2010, Jun-15, Volume: 25, Issue:8

    Topics: Child, Preschool; Dihydroxyphenylalanine; DNA Mutational Analysis; Greece; Homovanillic Acid; Humans

2010