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2. Urinary excretion of total cystine and the dibasic amino acids arginine, lysine and ornithine in relation to genetic findings in patients with cystinuria treated with sulfhydryl compounds. Fjellstedt E, Harnevik L, Jeppsson JO, Tiselius HG, Söderkvist P, Denneberg T. Urol Res; 2003 Dec; 31(6):417-25. PubMed ID: 14586528 [Abstract] [Full Text] [Related]
3. Cystinuria phenotyping by oral lysine and arginine loading. de Sanctis L, Bonetti G, Bruno M, De Luca F, Bisceglia L, Palacin M, Dianzani I, Ponzone A. Clin Nephrol; 2001 Dec; 56(6):467-74. PubMed ID: 11770798 [Abstract] [Full Text] [Related]
13. The excretion of amino acids by cystinuric patients and their relatives. Crawhall JC, Purkiss P, Watts RW, Young EP. Ann Hum Genet; 1969 Oct 28; 33(2):149-69. PubMed ID: 5383982 [No Abstract] [Full Text] [Related]
15. Diagnostic and genetic studies in 43 patients with classic cystinuria. Byrd DJ, Lind M, Brodehl J. Clin Chem; 1991 Jan 28; 37(1):68-73. PubMed ID: 1899064 [Abstract] [Full Text] [Related]