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Journal Abstract Search

1002 related items for PubMed ID: 16468607

  • 1.
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  • 2. Collagen type IV nephropathy: genetic heterogeneity examinations in affected Hungarian families.
    Endreffy E, Ondrik Z, Iványi B, Maróti Z, Bereczki C, Haszon I, Györke Z, Worum E, Németh K, Rikker C, Ökrös Z, Túri S.
    Mol Cell Probes; 2011 Feb; 25(1):28-34. PubMed ID: 20951199
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  • 3. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 4. Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically.
    Imafuku A, Nozu K, Sawa N, Hasegawa E, Hiramatsu R, Kawada M, Hoshino J, Tanaka K, Ishii Y, Takaichi K, Fujii T, Ohashi K, Iijima K, Ubara Y.
    Nephrology (Carlton); 2018 Oct; 23(10):940-947. PubMed ID: 28704582
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  • 5. Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and clinical outcome.
    Marcocci E, Uliana V, Bruttini M, Artuso R, Silengo MC, Zerial M, Bergesio F, Amoroso A, Savoldi S, Pennesi M, Giachino D, Rombolà G, Fogazzi GB, Rosatelli C, Martinhago CD, Carmellini M, Mancini R, Di Costanzo G, Longo I, Renieri A, Mari F.
    Nephrol Dial Transplant; 2009 May; 24(5):1464-71. PubMed ID: 19129241
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  • 7. 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. Spectrum of collagen type IV nephropathies: from thin basement membrane nephropathy to Alport syndrome.
    Vizjak A, Ferluga D.
    Srp Arh Celok Lek; 2008 Dec; 136 Suppl 4():323-6. PubMed ID: 20804103
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  • 11. 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; 21(3):665-71. PubMed ID: 16338941
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  • 14. Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.
    Papazachariou L, Papagregoriou G, Hadjipanagi D, Demosthenous P, Voskarides K, Koutsofti C, Stylianou K, Ioannou P, Xydakis D, Tzanakis I, Papadaki A, Kallivretakis N, Nikolakakis N, Perysinaki G, Gale DP, Diamantopoulos A, Goudas P, Goumenos D, Soloukides A, Boletis I, Melexopoulou C, Georgaki E, Frysira E, Komianou F, Grekas D, Paliouras C, Alivanis P, Vergoulas G, Pierides A, Daphnis E, Deltas C.
    Clin Genet; 2017 Nov; 92(5):517-527. PubMed ID: 28632965
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  • 17. Alport syndrome and thin basement membrane nephropathy.
    Thorner PS.
    Nephron Clin Pract; 2007 Nov; 106(2):c82-8. PubMed ID: 17570934
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  • 18. COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome.
    Buzza M, Wang YY, Dagher H, Babon JJ, Cotton RG, Powell H, Dowling J, Savige J.
    Kidney Int; 2001 Aug; 60(2):480-3. PubMed ID: 11473630
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  • 20. Chronic renal failure and shortened lifespan in COL4A3+/- mice: an animal model for thin basement membrane nephropathy.
    Beirowski B, Weber M, Gross O.
    J Am Soc Nephrol; 2006 Jul; 17(7):1986-94. PubMed ID: 16775036
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