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Journal Abstract Search

81 related items for PubMed ID: 4470916

  • 1. The genetics of the Alport syndrome.
    Tishler PV, Rosner B.
    Birth Defects Orig Artic Ser; 1974; 10(4):93-9. PubMed ID: 4470916
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  • 3. Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome.
    Shaw EA, Colville D, Wang YY, Zhang KW, Dagher H, Fassett R, Guymer R, Savige J.
    Nephrol Dial Transplant; 2007 Jan; 22(1):104-8. PubMed ID: 17071739
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  • 5. [Collagen type IV nephropathy: from thin basement membrane nephropathy to Alport syndrome].
    Endreffy E, Ondrik Z, Kemény E, Vas Z, Maróti Z, Lencse G, Bereczki C, Haszon I, Túri S, Iványi B.
    Orv Hetil; 2005 Dec 25; 146(52):2647-53. PubMed ID: 16468607
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  • 8. [Alport syndrome in the light of current molecular genetics].
    Pirson Y.
    Bull Mem Acad R Med Belg; 1996 Dec 25; 151(10-11):447-52; discussion 452-3. PubMed ID: 9491622
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  • 9. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 25; 56(3):105-52. PubMed ID: 19728970
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  • 10. Autosomal dominant Alport's syndrome: study of a large Tunisian family.
    Kharrat M, Makni S, Makni K, Kammoun K, Charfeddine K, Azaeiz H, Jarraya F, Ben Hmida M, Gubler MC, Ayadi H, Hachicha J.
    Saudi J Kidney Dis Transpl; 2006 Sep 25; 17(3):320-5. PubMed ID: 16970251
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  • 12. Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families.
    Longo I, Scala E, Mari F, Caselli R, Pescucci C, Mencarelli MA, Speciale C, Giani M, Bresin E, Caringella DA, Borochowitz ZU, Siriwardena K, Winship I, Renieri A, Meloni I.
    Nephrol Dial Transplant; 2006 Mar 25; 21(3):665-71. PubMed ID: 16338941
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  • 15. Type IV collagen alpha 5 chain. Normal distribution and abnormalities in X-linked Alport syndrome revealed by monoclonal antibody.
    Yoshioka K, Hino S, Takemura T, Maki S, Wieslander J, Takekoshi Y, Makino H, Kagawa M, Sado Y, Kashtan CE.
    Am J Pathol; 1994 May 25; 144(5):986-96. PubMed ID: 8178947
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  • 18. The retinal "lozenge" or "dull macular reflex" in Alport syndrome may be associated with a severe retinopathy and early-onset renal failure.
    Colville D, Wang YY, Tan R, Savige J.
    Br J Ophthalmol; 2009 Mar 25; 93(3):383-6. PubMed ID: 19019929
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  • 19. 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 25; 22(5):1338-46. PubMed ID: 17277342
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  • 20. [Alport syndrome or progressive hereditary nephritis with hearing loss].
    Gubler MC, Heidet L, Antignac C.
    Nephrol Ther; 2007 Jun 25; 3(3):113-20. PubMed ID: 17540313
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