Page last updated: 2024-10-16

carnitine and Cystinuria

carnitine 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 Excerpts

ExcerptRelevanceReference
"Cystinuria is a rare inherited renal stone disease caused by mutations in the SLC3A1 and SLC7A9 genes."1.48Clinical, Biochemical, and Genetic Findings of Cystinuria in Chinese Children. ( Li, D; Li, XY; Liu, YP; Ma, YY; Song, JQ; Yang, YL, 2018)

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
Ma, YY1
Liu, YP1
Li, D1
Li, XY1
Song, JQ1
Yang, YL1

Other Studies

1 other study available for carnitine and Cystinuria

ArticleYear
Clinical, Biochemical, and Genetic Findings of Cystinuria in Chinese Children.
    Clinical laboratory, 2018, Jul-01, Volume: 64, Issue:7

    Topics: Adolescent; Amino Acid Transport Systems, Basic; Amino Acid Transport Systems, Neutral; Amino Acids;

2018