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Journal Abstract Search

204 related items for PubMed ID: 8463902

  • 1. Prospective analysis and classification of patients with cystinuria identified in a newborn screening program.
    Goodyer PR, Clow C, Reade T, Girardin C.
    J Pediatr; 1993 Apr; 122(4):568-72. PubMed ID: 8463902
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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
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  • 3. Reference values of urinary excretion of cystine and dibasic aminoacids: classification of patients with cystinuria in the Valencian Community, Spain.
    Guillén M, Corella D, Cabello ML, García AM, Hernández-Yago J.
    Clin Biochem; 1999 Feb; 32(1):25-30. PubMed ID: 10074888
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  • 4. Ontogeny modifies manifestations of cystinuria genes: implications for counseling.
    Scriver CR, Clow CL, Reade TM, Goodyer P, Auray-Blais C, Giguère R, Lemieux B.
    J Pediatr; 1985 Mar; 106(3):411-6. PubMed ID: 3919167
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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. Cystinuria subtype and the risk of nephrolithiasis.
    Goodyer P, Saadi I, Ong P, Elkas G, Rozen R.
    Kidney Int; 1998 Jul; 54(1):56-61. PubMed ID: 9648063
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  • 13. Cystinuria: genetic heterogeneity and allelism.
    Rosenberg LE.
    Science; 1966 Dec 09; 154(3754):1341-3. PubMed ID: 5925065
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  • 17. A mouse model for cystinuria type I.
    Peters T, Thaete C, Wolf S, Popp A, Sedlmeier R, Grosse J, Nehls MC, Russ A, Schlueter V.
    Hum Mol Genet; 2003 Sep 01; 12(17):2109-20. PubMed ID: 12923163
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