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Journal Abstract Search

155 related items for PubMed ID: 4467473

  • 1. [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; 13(6):137-44. PubMed ID: 4467473
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  • 3. [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
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  • 5. [Alport's syndrome in twins].
    Syrenicz A, Czekalski S, Majkowska L.
    Pol Tyg Lek; 1980; 46(43-44):844-6. PubMed ID: 1669176
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  • 6. [Chronic hereditary nephritis with hearing loss (Alport's syndrome)].
    Zientalska-Rumińska E, Stankiewicz-Szymczak W, Moszyński B.
    Otolaryngol Pol; 1989; 43(5-6):401-8. PubMed ID: 2640496
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  • 9. Hereditary hearing loss with nephropathy (Alport's syndrome).
    Turner JS.
    Acta Otolaryngol Suppl; 1970; 271():1-26. PubMed ID: 5278250
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  • 10. [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
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  • 11. Alport's syndrome (progressive hereditary nephritis).
    Gaboardi F, Edefonti A, Imbasciati E, Tarantino A, Mihatsch MJ, Zollinger HU.
    Clin Nephrol; 1974 Apr; 2(4):143-56. PubMed ID: 4603152
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  • 12. Genetic features of Alport's syndrome.
    Schröder CH, Brunner H, Monnens LA.
    Contrib Nephrol; 1990 Apr; 80():3-8. PubMed ID: 2282819
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  • 13. [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 Apr; 67(4):45-7. PubMed ID: 7784975
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  • 18. Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties.
    Colville D, Wang YY, Jamieson R, Collins F, Hood J, Savige J.
    Ophthalmic Genet; 2000 Dec; 21(4):217-25. PubMed ID: 11135492
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  • 19. [Fechtner syndrome. A rare differential Alport syndrome diagnosis].
    Delb W, Schenk J, Iro H.
    HNO; 2000 Aug; 48(8):616-20. PubMed ID: 10994174
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