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Journal Abstract Search

209 related items for PubMed ID: 10584551

  • 1. [X chromosome dominant hereditary nephritis: characterization by pedigree analysis and simple studies in general practice].
    Wälchli P.
    Praxis (Bern 1994); 1999 Oct 28; 88(44):1811-4. PubMed ID: 10584551
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  • 4. Renal prognosis in Alport's and related syndromes: influence of the mode of inheritance.
    Pochet JM, Bobrie G, Landais P, Goldfarb B, Grünfeld JP.
    Nephrol Dial Transplant; 1989 Oct 28; 4(12):1016-21. PubMed ID: 2517321
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  • 7. [Alport's syndrome: apropos of 2 families].
    Grünfeld JP.
    Nephrologie; 2000 Oct 28; 21(6):295-8. PubMed ID: 11117109
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  • 8. Hereditary nephritis in the bull terrier: evidence for inheritance by an autosomal dominant gene.
    Hood JC, Robinson WF, Huxtable CR, Bradley JS, Sutherland RJ, Thomas MA.
    Vet Rec; 1990 May 05; 126(18):456-9. PubMed ID: 2356601
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  • 9. A comparison of the clinical, histopathologic, and ultrastructural phenotypes in carriers of X-linked and autosomal recessive Alport's syndrome.
    Dagher H, Buzza M, Colville D, Jones C, Powell H, Fassett R, Wilson D, Agar J, Savige J.
    Am J Kidney Dis; 2001 Dec 05; 38(6):1217-28. PubMed ID: 11728953
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  • 10. A novel Cys1638Tyr NC1 domain substitution in alpha5(IV) collagen causes Alport syndrome with late onset renal failure without hearing loss or eye abnormalities.
    Wilson JC, Yoon HS, Walker RJ, Eccles MR.
    Nephrol Dial Transplant; 2007 May 05; 22(5):1338-46. PubMed ID: 17277342
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  • 11. Hereditary glomerulonephritis of non-Alport type.
    Doherty CC, Middleton DT, Hill CM.
    Proc Eur Dial Transplant Assoc; 1983 May 05; 19():575-81. PubMed ID: 6878256
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  • 12. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 05; 56(3):105-52. PubMed ID: 19728970
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  • 14. [Late hereditary degenerative sensorineural hearing loss associated with IgA mesangial glomerulonephritis of probable autosomal dominant heredity].
    de Serdio JL, Chahin J, Gil-Curbelo JA, Perera A, Saavedra JA.
    Acta Otorrinolaringol Esp; 1993 Aug 05; 44(6):447-54. PubMed ID: 8155361
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  • 15. [Hereditary nephritis with bearing loss of the receiver type (Alport's syndrome) with a description of 2 cases].
    Zhelev N, Astrug A, Konstantinova B, Henov D.
    Vutr Boles; 1974 Aug 05; 13(6):137-44. PubMed ID: 4467473
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  • 19. 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 05; 3(7):488-91. PubMed ID: 11791413
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  • 20. Hereditary nephritis with macrothrombocytopenia: phenotypic variety and the genotypic defect.
    Basile C, Schiavone P, Heidet L, Grünfeld JP.
    J Nephrol; 2002 Jul 05; 15(3):320-3. PubMed ID: 12113606
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