Results 181 to 190 of about 6,097 (205)
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Cystinuria and Dermatomyositis
Clinical Pediatrics, 1970A girl is described who had both cystinuria and dermatomyositis. This associa tion, not previously recorded, may or may not be pathogenetically related.
Nancy P. Fawcett, William L. Nyhan
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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 the American Veterinary Medical Association, 1991
A 10-month-old male Siamese cat with dysuria was determined to have cystine crystalluria. Many small calculi composed entirely of cystine were found in the urinary bladder. Measurement of serum and urine amino acids and calculation of fractional reabsorption of amino acids indicated reabsorption defects for cystine, ornithine, lysine, and arginine ...
S P, DiBartola, D J, Chew, M L, Horton
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A 10-month-old male Siamese cat with dysuria was determined to have cystine crystalluria. Many small calculi composed entirely of cystine were found in the urinary bladder. Measurement of serum and urine amino acids and calculation of fractional reabsorption of amino acids indicated reabsorption defects for cystine, ornithine, lysine, and arginine ...
S P, DiBartola, D J, Chew, M L, Horton
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Endocrinology and Metabolism Clinics of North America, 1990
Cystinuria is an hereditary disorder of renal and intestinal transport characterized by the excessive urinary excretion of cystine, arginine, lysine, and ornithine. It is inherited as a common recessive gene with allelic mutations. Complementary studies of the plasma response to oral cystine loading, intestinal mucosal transport patterns, and urine ...
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Cystinuria is an hereditary disorder of renal and intestinal transport characterized by the excessive urinary excretion of cystine, arginine, lysine, and ornithine. It is inherited as a common recessive gene with allelic mutations. Complementary studies of the plasma response to oral cystine loading, intestinal mucosal transport patterns, and urine ...
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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.
Samer Kalakish +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.
Samer Kalakish +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.
Rizzoni G +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.
Rizzoni G +6 more
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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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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 ...
Giorcelli G +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 ...
Giorcelli G +6 more
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A case of congenital cystinuria
The Journal of Pediatrics, 1952Summary A case is described of congenital cystinuria with associated lysinuria and cystine and oxalate calculosis in a 3-year-old boy. Disturbances of micturition caused by bladder stones started as early as the age of 2 years. The observations point to a disturbance in the tubular reabsorption of cystine and lysine.
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