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Journal Abstract Search

322 related items for PubMed ID: 7454376

  • 1. [Pedigree analysis of two families with Alport's syndrome].
    Wässer S, Theile H, Schöne D, Lemme B.
    Padiatr Grenzgeb; 1980; 19(3):167-71. PubMed ID: 7454376
    [No Abstract] [Full Text] [Related]

  • 2. [Alport's syndrome: hereditary nephropathy with hematuria and deafness].
    Giger C, Guignard JP, Pelet B, Campiche M, Krstic R.
    Rev Med Suisse Romande; 1988 Apr; 108(4):349-55. PubMed ID: 3387770
    [No Abstract] [Full Text] [Related]

  • 3. Hereditary nephropathy with hearing loss. "Alport's syndrome".
    Iversen UM.
    Acta Paediatr Scand Suppl; 1974 Apr; (245):1-23. PubMed ID: 4617477
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  • 6. [Hereditary nephritis (Alport's syndrome). Clinical, histological, ultrastructural and immunohistological study].
    Imbasciati E, Gaboardi F, Limido D, Tarantino A, Chiccoli C.
    Minerva Nefrol; 1973 Apr; 20(3):148-61. PubMed ID: 4586688
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  • 11. [2 families with Alport's syndrome].
    Cohen-Solal J, Delepierre M, Delepierre F, Herrault A.
    Ann Pediatr (Paris); 1970 Nov 02; 17(11):734-49. PubMed ID: 5484618
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  • 14. [Alport's syndrome (hereditary nephritis with deafness].
    Daneels R, Kuipers FC, Trimbos JB.
    Ned Tijdschr Geneeskd; 1967 Oct 21; 111(42):1870-9. PubMed ID: 6063763
    [No Abstract] [Full Text] [Related]

  • 15. [Hereditary nephritis (Alport's syndrome). Description of a family].
    Marcen Letosa R, Fdez Alonso J, Quereda Rguez navarro C, López Checa F, Castilla Jiménez J, Rodríguez Algarra G, Maceira Cruz B, Pereira Palomo P, Mateos Aguilar J.
    Rev Clin Esp; 1977 Nov 15; 147(3):291-6. PubMed ID: 605240
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  • 17. Hereditary nephritis witj h perceptive deafness (Alport's syndrome).
    Lachhein L, Büttner H, Kennitz P, Thal W, Witkowski R.
    Ger Med Mon; 1969 May 15; 14(5):218-22. PubMed ID: 5807504
    [No Abstract] [Full Text] [Related]

  • 18. [Alport's syndrome with mental retardation and purine metabolism disorders].
    Chodorowski Z, Natoński A.
    Pol Tyg Lek; 1979 May 14; 34(20):789-91. PubMed ID: 471814
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  • 19. [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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  • 20. [Alport's syndrome: apropos of 8 Tunisian families].
    el Matri A, Kechrid C, Ben Abdallah T, Ben Moussa F, Khder A, Ben Maiz H, Ben Ayed H.
    Tunis Med; 1988 May 28; 66(5):453-7. PubMed ID: 3061089
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