Page last updated: 2024-10-20

taurine and Cystinuria

taurine has been researched along with Cystinuria in 8 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
"The taurine deficiency was reversed by a change in diet or methionine supplementation."1.32Taurine deficiency in Newfoundlands fed commercially available complete and balanced diets. ( Backus, RC; Cohen, G; Fascetti, AJ; Good, KL; Pion, PD; Rogers, QR, 2003)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19904 (50.00)18.7374
1990's2 (25.00)18.2507
2000's2 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
HAMBRAEUS, L1
Backus, RC1
Cohen, G1
Pion, PD1
Good, KL1
Rogers, QR1
Fascetti, AJ1
Faggiano, A1
Melis, D1
Alfieri, R1
De Martino, M1
Filippella, M1
Milone, F1
Lombardi, G1
Colao, A1
Pivonello, R1
Rödenbeck, D1
Byrd, DJ1
Brodehl, J1
Jellum, E1
Thorsrud, AK1
Time, E1
King, JS2
Wainer, A1
Crawhall, JC1
Saunders, EP1
Thompson, CJ1

Other Studies

8 other studies available for taurine and Cystinuria

ArticleYear
CYSTINURIA IN SWEDEN. X. QUANTITATIVE STUDIES ON THE URINARY AMINO ACID EXCRETION IN CYSTINURICS.
    Acta Societatis Medicorum Upsaliensis, 1964, Volume: 69

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Arginine; Child; Chromatography; Cystinuria; Geria

1964
Taurine deficiency in Newfoundlands fed commercially available complete and balanced diets.
    Journal of the American Veterinary Medical Association, 2003, Oct-15, Volume: 223, Issue:8

    Topics: Animal Feed; Animal Nutritional Physiological Phenomena; Animals; Breeding; Cardiomyopathy, Dilated;

2003
Sulfur amino acids in Cushing's disease: insight in homocysteine and taurine levels in patients with active and cured disease.
    The Journal of clinical endocrinology and metabolism, 2005, Volume: 90, Issue:12

    Topics: Adult; Blood Glucose; Cross-Sectional Studies; Cystine; Cystinuria; Fasting; Female; Homocysteine; H

2005
The plasma concentration and renal handling of taurine in healthy children and in pediatric patients with disturbed sulfur metabolism.
    Advances in experimental medicine and biology, 1994, Volume: 359

    Topics: Adolescent; Child; Child, Preschool; Cystinosis; Cystinuria; Homocystinuria; Humans; Infant; Infant,

1994
Capillary electrophoresis for diagnosis and studies of human disease, particularly metabolic disorders.
    Journal of chromatography, 1991, Oct-18, Volume: 559, Issue:1-2

    Topics: Biopsy; Chromatography, High Pressure Liquid; Cystinuria; Electrophoresis; Homocystinuria; Humans; M

1991
Cystinuria with hyperuricemia and methioninuria. Biochemical study of a case.
    The American journal of medicine, 1967, Volume: 43, Issue:1

    Topics: Adult; Amino Acids; Cystinuria; Female; Homocysteine; Humans; Kidney Calculi; Methionine; Penicillam

1967
Treatment of cystinuria with alpha-mercaptopropionylglycine: a preliminary report with some notes on column chromatography of mercaptans.
    Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 1968, Volume: 129, Issue:3

    Topics: Amino Acids; Chromatography; Cysteine; Cystinuria; Humans; Taurine

1968
Heterozygotes for cystinuria.
    Annals of human genetics, 1966, Volume: 29, Issue:3

    Topics: Adolescent; Adult; Aged; Alanine; Amino Acids; Animals; Arginine; Child; Chromatography, Thin Layer;

1966