Results 231 to 240 of about 8,821 (269)
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Clinical Science, 1974
1. By using ion-exchange columns coupled to a sensitive automated Sakaguchi reaction, in addition to the normal ninhydrin reaction for amino acids, homoarginine, a guanidino homologue of arginine, was found in the plasma and urine of both normal and cystinuric individuals. 2. In all seven cystinuric subjects studied, urinary excretion of
B D, Cox, J S, Cameron
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1. By using ion-exchange columns coupled to a sensitive automated Sakaguchi reaction, in addition to the normal ninhydrin reaction for amino acids, homoarginine, a guanidino homologue of arginine, was found in the plasma and urine of both normal and cystinuric individuals. 2. In all seven cystinuric subjects studied, urinary excretion of
B D, Cox, J S, Cameron
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Journal of Endourology, 1997
We compared quantitative urinary cystine values in stone-forming family members and unaffected relatives based on an index stone-forming patient. A family pedigree of 39 members was identified. Quantitative urinalyses and serum biochemical profiles were collected with the subjects on similar diets over 72 hours. Detailed medical histories were obtained.
M L, Stoller +4 more
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We compared quantitative urinary cystine values in stone-forming family members and unaffected relatives based on an index stone-forming patient. A family pedigree of 39 members was identified. Quantitative urinalyses and serum biochemical profiles were collected with the subjects on similar diets over 72 hours. Detailed medical histories were obtained.
M L, Stoller +4 more
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Urologic Clinics of North America, 2007
Cystinuria is a monogenic disorder in which there is a transepithelial transport defect of di-basic amino acids, including cystine, ornithine, lysine, and arginine (COLA). This results in diminished reabsorption of these amino acids in both the intestine and renal proximal tubule.
Alexandra, Rogers +3 more
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Cystinuria is a monogenic disorder in which there is a transepithelial transport defect of di-basic amino acids, including cystine, ornithine, lysine, and arginine (COLA). This results in diminished reabsorption of these amino acids in both the intestine and renal proximal tubule.
Alexandra, Rogers +3 more
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European Urology, 1981
7 children, 20 months to 11 years old, with cystinuria and renal calculi were studied. Surgical treatment and alpha-mercaptopropionylglycine (MPG) gave satisfactory results in 5 children. The causes of the recurrences in the other 2 children are discussed.
L, Pavanello +6 more
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7 children, 20 months to 11 years old, with cystinuria and renal calculi were studied. Surgical treatment and alpha-mercaptopropionylglycine (MPG) gave satisfactory results in 5 children. The causes of the recurrences in the other 2 children are discussed.
L, Pavanello +6 more
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Re: Cystinuria: Genetic Aspects, Mouse Models, and a New Approach to Therapy.
Journal of Urology, 2019available at http://www.ncbi.nlm.nih.gov/pubmed/30515543 Editorial Comment: Cystinuria is a genetic disease associated with abnormal amino acid (cystine, ornithine, lysine and arginine) transport in the kidney and gut.
D. Assimos
semanticscholar +1 more source
In Analysis, 2019
A unique metal-organic framework with the formula [Cd4(H2L)2(L)·H2O]·3H2O (H4L = 5,5'-(1H-1,2,4-triazole-3,5-diyl)diisophthalic acid) was successfully constructed under solvothermal conditions. The frameworks with multiple free Lewis base sites and Lewis
semanticscholar +1 more source
A unique metal-organic framework with the formula [Cd4(H2L)2(L)·H2O]·3H2O (H4L = 5,5'-(1H-1,2,4-triazole-3,5-diyl)diisophthalic acid) was successfully constructed under solvothermal conditions. The frameworks with multiple free Lewis base sites and Lewis
semanticscholar +1 more source
BJU International, 2019
To evaluate medical treatments, in terms of adverse events (AEs) and therapeutic goals, in a large series of patients with cystinuria.
Caroline Prot-Bertoye +34 more
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To evaluate medical treatments, in terms of adverse events (AEs) and therapeutic goals, in a large series of patients with cystinuria.
Caroline Prot-Bertoye +34 more
semanticscholar +1 more source
, 2020
Selective sensing of biothiols holds immense importance due to the adverse roles of abnormal concentrations of biothiols in several diseases, henceforth demanding widespread research for developing a sensory receptor towards the selective detection of ...
Sourav Bej +5 more
semanticscholar +1 more source
Selective sensing of biothiols holds immense importance due to the adverse roles of abnormal concentrations of biothiols in several diseases, henceforth demanding widespread research for developing a sensory receptor towards the selective detection of ...
Sourav Bej +5 more
semanticscholar +1 more source
1980
Cystinuria is an inherited disorder of the tubular and jejunal mucosa transport of four amino acids:cys, lys, arg and ornithine (1–2). The association of cystinuria with other chronic diseases or metabolic disorders is not common. Therefore it seemed us usefull to present the association hyperuricemia and cystinuria in 7 out of 55 cystinic lithiasis ...
F, Linari +6 more
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Cystinuria is an inherited disorder of the tubular and jejunal mucosa transport of four amino acids:cys, lys, arg and ornithine (1–2). The association of cystinuria with other chronic diseases or metabolic disorders is not common. Therefore it seemed us usefull to present the association hyperuricemia and cystinuria in 7 out of 55 cystinic lithiasis ...
F, Linari +6 more
openaire +2 more sources
Rapid detection of the biomarker for cystinuria by a metal-organic framework fluorescent sensor.
Talanta: The International Journal of Pure and Applied Analytical Chemistry, 2023Li Peng +8 more
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