Page last updated: 2024-10-16

choline and Cystinuria

choline has been researched along with Cystinuria in 3 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 (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	3 (100.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
COXON, V	1
KOLB, FO	1
LANGENSKIOLD, A	1
ZINSSER, HH	1

Other Studies

3 other studies available for choline and Cystinuria

Article	Year
The use of oral choline in cystinuria. Metabolism: clinical and experimental, 1954, Volume: 3, Issue:3 Topics: Choline; Cystine; Cystinuria; Humans	1954
Cystinuria and cystine lithiasis; the influence of choline on cystine excretion. Annales chirurgiae et gynaecologiae Fenniae, 1954, Volume: 43, Issue:2 Topics: Biological Transport; Body Fluids; Calculi; Choline; Cystine; Cystinuria; Humans; Kidney; Kidney Cal	1954
The effect of oral choline in reducing cystine excretion in cystinuria: a report of two cases. The Journal of urology, 1950, Volume: 63, Issue:5 Topics: Choline; Cystine; Cystinuria; Humans; Urine	1950