Page last updated: 2024-11-05

tyramine and Cystinuria

tyramine has been researched along with Cystinuria in 1 studies

Cystinuria: An inherited disorder due to defective reabsorption of CYSTINE and other BASIC AMINO ACIDS by the PROXIMAL RENAL TUBULES. This form of aminoaciduria is characterized by the abnormally high urinary levels of cystine; LYSINE; ARGININE; and ORNITHINE. Mutations involve the amino acid transport protein gene SLC3A1.

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
TOMPSETT, SL1

Other Studies

1 other study available for tyramine and Cystinuria

ArticleYear
The use of a cation-exchange resin in the determination of some basic substances (tyrosine, tyramine, kynurenine, 3-hydroxykynurenine and cystine) in urine.
    Clinica chimica acta; international journal of clinical chemistry, 1962, Volume: 7

    Topics: Body Fluids; Cations; Cystinuria; Humans; Ion Exchange Resins; Kynurenine; Tyramine; Tyrosine

1962