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Effect of urine alkalization on urinary inflammatory markers in cystinuric patients. [PDF]
Clin Kidney JProt-Bertoye C +9 more
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Coexisting elastosis perforans serpiginosa and acquired cutis laxa following long-term penicillamine in Wilson disease. [PDF]
Skin Health DisMa TA, Van Rooij N.
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Increased efficacy in lower pole stone management with a novel flexible and navigable suction ureteral access sheath with flexible ureteroscopic lithotripsy: a case series. [PDF]
Transl Androl UrolXiong L +5 more
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Seminars in Nephrology, 2008
Cystinuria is an inherited disorder characterized by the impaired reabsorption of cystine in the proximal tubule of the nephron and the gastrointestinal epithelium. The only clinically significant manifestation is recurrent nephrolithiasis secondary to the poor solubility of cystine in urine.
Aditya, Mattoo, David S, Goldfarb
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Cystinuria is an inherited disorder characterized by the impaired reabsorption of cystine in the proximal tubule of the nephron and the gastrointestinal epithelium. The only clinically significant manifestation is recurrent nephrolithiasis secondary to the poor solubility of cystine in urine.
Aditya, Mattoo, David S, Goldfarb
openaire +3 more sources
CRC Critical Reviews in Clinical Laboratory Sciences, 1988
Cystinuria is an inherited metabolic disease resulting in renal stone formation. An incidence of 1 in 7000 makes it a relatively common genetic disease. The biochemical defect is a carrier protein in the epithelial cells of certain organs. This carrier protein is responsible for the transport of cystine and the dibasic amino acids.
Ronald D. Feld, Zakariya K. Shihabi
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Cystinuria is an inherited metabolic disease resulting in renal stone formation. An incidence of 1 in 7000 makes it a relatively common genetic disease. The biochemical defect is a carrier protein in the epithelial cells of certain organs. This carrier protein is responsible for the transport of cystine and the dibasic amino acids.
Ronald D. Feld, Zakariya K. Shihabi
openaire +2 more sources
Acta Paediatrica, 2006
AbstractCystinuria is an autosomal recessive disorder characterized by impaired transport of cystine, lysine, ornithine and arginine in the proximal renal tubule and in the epithelial cells of the gastrointestinal tract. Following recent progress in the genetic understanding of the disease, the traditional classification, based on the excretion of ...
Luca, Dello Strologo +1 more
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AbstractCystinuria is an autosomal recessive disorder characterized by impaired transport of cystine, lysine, ornithine and arginine in the proximal renal tubule and in the epithelial cells of the gastrointestinal tract. Following recent progress in the genetic understanding of the disease, the traditional classification, based on the excretion of ...
Luca, Dello Strologo +1 more
openaire +2 more sources