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Journal Abstract Search

156 related items for PubMed ID: 765939

  • 1. [Alport's-syndrome: diagnosis, light- and electronmicroscopic findings (author's transl)].
    Balzar E, Lubec G, Syŕe G, Weissenbacher G.
    Padiatr Padol; 1976; 11(1):221-33. PubMed ID: 765939
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  • 3. Alport's syndrome (progressive hereditary nephritis).
    Gaboardi F, Edefonti A, Imbasciati E, Tarantino A, Mihatsch MJ, Zollinger HU.
    Clin Nephrol; 1974; 2(4):143-56. PubMed ID: 4603152
    [No Abstract] [Full Text] [Related]

  • 4. Recent developments in hereditary nephritis (Alport's syndrome).
    Bubalo FS, Davidson DD.
    Indiana Med; 1991 Dec; 84(12):860-6. PubMed ID: 1774457
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  • 5. [Significance of family studies and kidney biopsies in children with renal hematuria].
    Pistor K, Bachmann H, Rumpelt HJ, Olbing H.
    Monatsschr Kinderheilkd; 1985 May; 133(5):269-73. PubMed ID: 4010678
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  • 8. Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis--a collaborative study of the Italian Renal Immunopathology Group.
    Frascà GM, Onetti-Muda A, Mari F, Longo I, Scala E, Pescucci C, Roccatello D, Alpa M, Coppo R, Li Volti G, Feriozzi S, Bergesio F, Schena FP, Renieri A, Italian Renal Immunopathology Group.
    Nephrol Dial Transplant; 2005 Mar; 20(3):545-51. PubMed ID: 15618242
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  • 10. Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome).
    Hinglais N, Grünfeld JP, Bois E.
    Lab Invest; 1972 Nov; 27(5):473-87. PubMed ID: 4653971
    [No Abstract] [Full Text] [Related]

  • 11. [Epidemiological study in 4 family units with Alport's syndrome].
    García-Delgado C, Gordillo-Paniagua G.
    Bol Med Hosp Infant Mex; 1981 Nov; 38(6):887-902. PubMed ID: 7317143
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  • 13. [3 cases of Alport's syndrome with different clinical and morphologic manifestations].
    Bechcińska B, Danilewicz M, Kałuzyński A, Marek K, Wagrowska-Danilewicz M.
    Patol Pol; 1989 Nov; 40(1):123-8. PubMed ID: 2477788
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  • 14. [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 Nov; 67(4):45-7. PubMed ID: 7784975
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  • 15. 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; 38(6):1217-28. PubMed ID: 11728953
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  • 16. [Recurrent hematuria in children].
    Dumas R, Baldet P, Bascoul S, Serres L, Jean R.
    Arch Fr Pediatr; 1978 Dec; 35(7):737-55. PubMed ID: 736729
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  • 17. Familial thin basement membrane nephropathy in children with asymptomatic microhematuria.
    Gauthier B, Trachtman H, Frank R, Valderrama E.
    Nephron; 1989 Dec; 51(4):502-8. PubMed ID: 2739828
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  • 18. [Alport's Syndrome. Hereditary nephritis, perceptive deafness and lens anomalies].
    Norrelund N.
    Ugeskr Laeger; 1971 Mar 19; 133(11):503-5. PubMed ID: 5092560
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  • 19. A Sri Lankan family with Alport's syndrome.
    Angunawela P, Mahamiththawa U.
    Ceylon Med J; 1998 Mar 19; 43(1):56-7. PubMed ID: 9624855
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  • 20. Alport's syndrome: experience at Hôpital Necker.
    Habib R, Gubler MC, Hinglais N, Noël LH, Droz D, Levy M, Mahieu P, Foidart JM, Perrin D, Bois E, Grünfeld JP.
    Kidney Int Suppl; 1982 May 19; 11():S20-8. PubMed ID: 6956772
    [Abstract] [Full Text] [Related]

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