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Journal Abstract Search

84 related items for PubMed ID: 1144845

  • 1. [Alport-Perkoff's syndrome. Study of a family].
    Cerezo Morales S, Hervás Sánchez JG, Asensio Peinado C, Martin Vivaldi G, Alonso Fernández J, Soriano Ortega C, Peña Yáñez A.
    Rev Clin Esp; 1975 Apr 30; 137(2):171-7. PubMed ID: 1144845
    [No Abstract] [Full Text] [Related]

  • 2. [Study of 3 families affected with Alport Perkoff's syndrome].
    Labella T, López E.
    An Otorrinolaringol Ibero Am; 1978 Apr 30; 5(1):35-52. PubMed ID: 665946
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  • 5. 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 30; 27(5):473-87. PubMed ID: 4653971
    [No Abstract] [Full Text] [Related]

  • 6. Evolution of glomerular basement membrane lesions in a male patient with Alport syndrome: ultrastructural and morphometric study.
    Cangiotti AM, Sessa A, Meroni M, Montironi R, Ragaiolo M, Mambelli V, Cinti S.
    Nephrol Dial Transplant; 1996 Sep 30; 11(9):1829-34. PubMed ID: 8918631
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  • 8. [Chronic hereditary nephropathy with deafness and ocular lesions].
    Hauser J.
    Schweiz Med Wochenschr; 1974 May 18; 104(20):724-8. PubMed ID: 4829630
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  • 11. The pathology of the kidney in the Alport syndrome.
    Spear GS.
    Birth Defects Orig Artic Ser; 1974 May 18; 10(4):109-13. PubMed ID: 4470885
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  • 14. [Alport-Perkoff's syndrome (two cases report)].
    Prieto Veiga J, Rosado T, Blázquez García J, Martín García M, De Manueles Jiménez J, Escribano Albarrán R, Salazar A-Villalobos V.
    An Esp Pediatr; 1977 Feb 18; 10(2):187-96. PubMed ID: 869343
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  • 15. 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 18; 3(7):488-91. PubMed ID: 11791413
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  • 17. Renal biopsy interpretation in Alport Syndrome.
    Mazzucco G, De Marchi M, Monga G.
    Semin Diagn Pathol; 2002 Aug 18; 19(3):133-45. PubMed ID: 12180634
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  • 18. [Alport-Perkoff syndrome. Clinical and ultramicroscopic study of a family].
    López Sánchez A, López Campos JL, Montagut Sánchez M, Delgado Yanes JC, Pérez Gúzman E, Pérez Cresco J, Bernaldo de Quirós J.
    Rev Clin Esp; 1974 Mar 15; 132(5):435-44. PubMed ID: 4831274
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  • 20. Hereditary hearing loss with nephropathy (Alport's syndrome).
    Turner JS.
    Acta Otolaryngol Suppl; 1970 Mar 15; 271():1-26. PubMed ID: 5278250
    [No Abstract] [Full Text] [Related]

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