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

Year Number of Results
1969 1
1974 2
1977 4
1980 1
1982 1
1983 2
1984 1
1985 1
1986 2
1988 2
1989 2
1990 5
1991 3
1992 9
1993 5
1994 10
1995 12
1996 14
1997 13
1998 12
1999 7
2000 19
2001 5
2002 5
2003 4
2004 5
2005 12
2006 6
2007 7
2008 3
2009 9
2010 6
2011 5
2012 9
2013 7
2014 6
2015 1
2016 7
2017 3
2018 4
2019 2
2020 7
2021 0
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Similar articles for PMID: 10752524

226 results
Results by year
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Page 1
X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.
Jais JP, Knebelmann B, Giatras I, De Marchi M, Rizzoni G, Renieri A, Weber M, Gross O, Netzer KO, Flinter F, Pirson Y, Verellen C, Wieslander J, Persson U, Tryggvason K, Martin P, Hertz JM, Schröder C, Sanak M, Krejcova S, Carvalho MF, Saus J, Antignac C, Smeets H, Gubler MC. Jais JP, et al. J Am Soc Nephrol. 2000 Apr;11(4):649-57. J Am Soc Nephrol. 2000. PMID: 10752524 Free article.
Alport syndrome. Molecular genetic aspects.
Hertz JM. Hertz JM. Dan Med Bull. 2009 Aug;56(3):105-52. Dan Med Bull. 2009. PMID: 19728970
Comparison of alpha5(IV) collagen chain expression in skin with disease severity in women with X-linked Alport syndrome.
Nakanishi K, Iijima K, Kuroda N, Inoue Y, Sado Y, Nakamura H, Yoshikawa N. Nakanishi K, et al. J Am Soc Nephrol. 1998 Aug;9(8):1433-40. J Am Soc Nephrol. 1998. PMID: 9697665 Free article.
[Alport syndrome or progressive hereditary nephritis with hearing loss].
Gubler MC, Heidet L, Antignac C. Gubler MC, et al. Nephrol Ther. 2007 Jun;3(3):113-20. doi: 10.1016/j.nephro.2007.03.005. Epub 2007 May 8. Nephrol Ther. 2007. PMID: 17540313 French.
X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study.
Jais JP, Knebelmann B, Giatras I, De Marchi M, Rizzoni G, Renieri A, Weber M, Gross O, Netzer KO, Flinter F, Pirson Y, Dahan K, Wieslander J, Persson U, Tryggvason K, Martin P, Hertz JM, Schröder C, Sanak M, Carvalho MF, Saus J, Antignac C, Smeets H, Gubler MC. Jais JP, et al. J Am Soc Nephrol. 2003 Oct;14(10):2603-10. doi: 10.1097/01.asn.0000090034.71205.74. J Am Soc Nephrol. 2003. PMID: 14514738 Free article.
Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome.
Hertz JM, Juncker I, Persson U, Matthijs G, Schmidtke J, Petersen MB, Kjeldsen M, Gregersen N. Hertz JM, et al. Hum Mutat. 2001 Aug;18(2):141-8. doi: 10.1002/humu.1163. Hum Mutat. 2001. PMID: 11462238
[Molecular genetics of Alport syndrome].
Yamazaki H, Saito A, Nakagawa Y, Arakawa M. Yamazaki H, et al. Nihon Rinsho. 1992 Dec;50(12):3021-6. Nihon Rinsho. 1992. PMID: 1491454 Review. Japanese.
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. Wilson JC, et al. Nephrol Dial Transplant. 2007 May;22(5):1338-46. doi: 10.1093/ndt/gfl793. Epub 2007 Feb 3. Nephrol Dial Transplant. 2007. PMID: 17277342
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. Marcocci E, et al. Nephrol Dial Transplant. 2009 May;24(5):1464-71. doi: 10.1093/ndt/gfn681. Epub 2009 Jan 7. Nephrol Dial Transplant. 2009. PMID: 19129241 Free article.
226 results
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