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Journal Abstract Search

100 related items for PubMed ID: 4831274

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  • 4. [Cryptorchism associated with hereditary nephritis: a 3-generation study in a Puerto Rican family].
    Senquiz AL, Corretjer JL, Vázquez J.
    Bol Asoc Med P R; 1990 Feb; 82(2):62-6. PubMed ID: 1969737
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  • 6. Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studies.
    Ilan T, Shohat T, Tobar A, Magal N, Yahav M, Halpern GJ, Rechavi G, Shohat M.
    Isr Med Assoc J; 2001 Jul; 3(7):488-91. PubMed ID: 11791413
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  • 7. [Contribution to the study of Alport's syndrome. Apropos of a case].
    Schneegans E, Rohmer A, Levy-Silagy J, el-Mejjati A, Sengel A, Stoebner P, Laforgue D.
    Ann Pediatr (Paris); 1971 Dec 14; 18(12):757-69. PubMed ID: 5004890
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  • 8. [The first experience in Russia of using DNA diagnosis in Alport's syndrome in a family with a unique morphological picture of the kidney lesion].
    Tsalikova FD, Ignatova MS, Krasnopol'skaia KD, Tverskaia SM, Brydun AV.
    Ter Arkh; 1995 Dec 14; 67(4):45-7. PubMed ID: 7784975
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  • 10. de-novo Alport syndrome: for the diagnosis of inherited glomerulonephritis with neither any family history nor extrarenal manifestation.
    Fukushima T, Nomura S, Kawai S, Osawa G.
    Clin Nephrol; 1997 Aug 14; 48(2):134-5. PubMed ID: 9285155
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  • 16. [Alport syndrome in 23-year-old woman].
    Finke D, Bilińska W, Kałuzyński A, Nowicki M.
    Pol Merkur Lekarski; 2008 Aug 14; 24 Suppl 4():22-4. PubMed ID: 18924495
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  • 17. De-novo COL4A5 gene mutations in Alport's syndrome.
    Massella L, Rizzoni G, De Blasis R, Barsotti P, Faraggiana T, Renieri A, Seri M, Galli L, De Marchi M.
    Nephrol Dial Transplant; 1994 Aug 14; 9(10):1408-11. PubMed ID: 7816253
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  • 18. The renal lesions of Alport syndrome.
    Heidet L, Gubler MC.
    J Am Soc Nephrol; 2009 Jun 14; 20(6):1210-5. PubMed ID: 19470679
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  • 20. Renal biopsy interpretation in Alport Syndrome.
    Mazzucco G, De Marchi M, Monga G.
    Semin Diagn Pathol; 2002 Aug 14; 19(3):133-45. PubMed ID: 12180634
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