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Journal Abstract Search

147 related items for PubMed ID: 939063

  • 1. Cystinuria: a new genetic variant.
    Stephens AD, Perrett D.
    Clin Sci Mol Med; 1976 Jul; 51(1):27-32. PubMed ID: 939063
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  • 2. Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria.
    Langen H, von Kietzell D, Byrd D, Arslan-Kirchner M, Vester U, Stuhrmann M, Dörk T, Saar K, Reis A, Schmidtke J, Brodehl J.
    Pediatr Nephrol; 2000 May; 14(5):376-84. PubMed ID: 10805464
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  • 3. Biochemical and genetic studies in cystinuria: observations on double heterozygotes of genotype I-II.
    Morin CL, Thompson MW, Jackson SH, Sass-Kortsak A.
    J Clin Invest; 1971 Sep; 50(9):1961-76. PubMed ID: 5564399
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  • 4. Diagnostic and genetic studies in 43 patients with classic cystinuria.
    Byrd DJ, Lind M, Brodehl J.
    Clin Chem; 1991 Jan; 37(1):68-73. PubMed ID: 1899064
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  • 5. 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
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  • 6. 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
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  • 13. Slc7a9-deficient mice develop cystinuria non-I and cystine urolithiasis.
    Feliubadaló L, Arbonés ML, Mañas S, Chillarón J, Visa J, Rodés M, Rousaud F, Zorzano A, Palacín M, Nunes V.
    Hum Mol Genet; 2003 Sep 01; 12(17):2097-108. PubMed ID: 12915471
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  • 15. Renal transport of lysine and arginine in cystinuria.
    Kato T.
    Tohoku J Exp Med; 1983 Jan 01; 139(1):9-16. PubMed ID: 6404004
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  • 18. Renal tubule reabsorption of amino acids after lysine loading of cystinuric dogs.
    Bovee KC, Segal S.
    Metabolism; 1984 Jul 01; 33(7):602-7. PubMed ID: 6429476
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