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Journal Abstract Search

236 related items for PubMed ID: 14201536

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  • 3. 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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  • 4. 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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  • 7. EVIDENCE AGAINST A SINGLE RENAL TRANSPORT DEFECT IN CYSTINURIA.
    FOX M, THIER S, ROSENBERG L, KISER W, SEGAL S.
    N Engl J Med; 1964 Mar 12; 270():556-61. PubMed ID: 14091528
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  • 11. CYSTINURIA: IN VITRO DEMONSTRATION OF AN INTESTINAL TRANSPORT DEFECT.
    THIER S, FOX M, SEGAL S, ROSENBERG LE.
    Science; 1964 Jan 31; 143(3605):482-4. PubMed ID: 14080318
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  • 15. [Cystine-lysine-ornithine-argininuria. Current genetic and clinico-therapeutic problems].
    Berio A.
    Minerva Pediatr; 1979 Oct 31; 31(20):1443-52. PubMed ID: 537610
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  • 16. CYSTINURIA IN SWEDEN. VIII. A CASE OF COELIAC DISEASE ASSOCIATED WITH CYSTINE-LYSINURIA.
    HAMBRAEUS L, DEHEVESY G.
    Acta Paediatr (Stockh); 1964 May 31; 53():213-20. PubMed ID: 14158474
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