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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 1
1991 1
1992 4
1993 8
1994 8
1995 10
1996 8
1997 3
1998 4
1999 4
2000 4
2001 5
2002 3
2003 2
2004 1
2005 4
2006 1
2007 2
2008 4
2009 3
2010 4
2011 4
2012 3
2013 4
2014 5
2015 4
2016 5
2017 6
2020 4
2021 4
2022 1
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Similar articles for PMID: 8738805

111 results
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Page 1
Identification of 17 mutations in ten exons in the COL4A5 collagen gene, but no mutations found in four exons in COL4A6: a study of 250 patients with hematuria and suspected of having Alport syndrome.
Heiskari N, Zhang X, Zhou J, Leinonen A, Barker D, Gregory M, Atkin CL, Netzer KO, Weber M, Reeders S, Grönhagen-Riska C, Neumann HP, Trembath R, Tryggvason K. Heiskari N, et al. J Am Soc Nephrol. 1996 May;7(5):702-9. doi: 10.1681/ASN.V75702. J Am Soc Nephrol. 1996. PMID: 8738805 Free article.
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome.
Renieri A, Galli L, Grillo A, Bruttini M, Neri T, Zanelli P, Rizzoni G, Massella L, Sessa A, Meroni M, Peratoner L, Riegler P, Scolari F, Mileti M, Giani M, Cossu M, Savi M, Ballabio A, De Marchi M. Renieri A, et al. Am J Med Genet. 1995 Nov 20;59(3):380-5. doi: 10.1002/ajmg.1320590320. Am J Med Genet. 1995. PMID: 8599366
Deletion of the 5'exons of COL4A6 is not needed for the development of diffuse leiomyomatosis in patients with Alport syndrome.
Sá MJ, Fieremans N, de Brouwer AP, Sousa R, e Costa FT, Brito MJ, Carvalho F, Rodrigues M, de Sousa FT, Felgueiras J, Neves F, Carvalho A, Ramos U, Vizcaíno JR, Alves S, Carvalho F, Froyen G, Oliveira JP. Sá MJ, et al. J Med Genet. 2013 Nov;50(11):745-53. doi: 10.1136/jmedgenet-2013-101670. Epub 2013 Aug 19. J Med Genet. 2013. PMID: 23958657
111 results