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

Year Number of Results
1973 1
1978 1
1979 1
1980 2
1981 2
1982 2
1984 2
1985 2
1986 3
1987 3
1988 5
1989 3
1990 5
1991 5
1992 4
1993 5
1994 6
1995 8
1996 6
1997 10
1998 7
1999 8
2000 9
2001 11
2002 6
2003 12
2004 14
2005 15
2006 20
2007 30
2008 18
2009 13
2010 35
2011 31
2012 45
2013 59
2014 69
2015 68
2016 93
2017 112
2018 117
2019 92
2020 85
2021 1
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Similar Articles for PMID: 21902819

919 results
Results by year
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Page 1
Atypical hemolytic uremic syndrome.
Loirat C, Frémeaux-Bacchi V. Loirat C, et al. Orphanet J Rare Dis. 2011 Sep 8;6:60. doi: 10.1186/1750-1172-6-60. Orphanet J Rare Dis. 2011. PMID: 21902819 Free PMC article. Review.
[Pathophysiology of atypical hemolytic uremic syndrome. Ten years of progress, from laboratory to patient].
Frémeaux-Bacchi V. Frémeaux-Bacchi V. Biol Aujourdhui. 2013;207(4):231-40. doi: 10.1051/jbio/2013027. Epub 2014 Mar 5. Biol Aujourdhui. 2013. PMID: 24594571 Review. French.
Genetic Atypical Hemolytic-Uremic Syndrome.
Noris M, Bresin E, Mele C, Remuzzi G. Noris M, et al. 2007 Nov 16 [updated 2016 Jun 9]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301541 Free Books & Documents. Review.
[Atypical hemolytic-uremic syndrome related to abnormalities within the complement system].
Frémeaux-Bacchi V, Fakhouri F, Roumenina L, Dragon-Durey MA, Loirat C. Frémeaux-Bacchi V, et al. Rev Med Interne. 2011 Apr;32(4):232-40. doi: 10.1016/j.revmed.2009.09.039. Epub 2011 Mar 3. Rev Med Interne. 2011. PMID: 21376430 French.
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.
Noris M, Caprioli J, Bresin E, Mossali C, Pianetti G, Gamba S, Daina E, Fenili C, Castelletti F, Sorosina A, Piras R, Donadelli R, Maranta R, van der Meer I, Conway EM, Zipfel PF, Goodship TH, Remuzzi G. Noris M, et al. Clin J Am Soc Nephrol. 2010 Oct;5(10):1844-59. doi: 10.2215/CJN.02210310. Epub 2010 Jul 1. Clin J Am Soc Nephrol. 2010. PMID: 20595690 Free PMC article.
Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome.
Fremeaux-Bacchi V, Moulton EA, Kavanagh D, Dragon-Durey MA, Blouin J, Caudy A, Arzouk N, Cleper R, Francois M, Guest G, Pourrat J, Seligman R, Fridman WH, Loirat C, Atkinson JP. Fremeaux-Bacchi V, et al. J Am Soc Nephrol. 2006 Jul;17(7):2017-25. doi: 10.1681/ASN.2005101051. Epub 2006 Jun 8. J Am Soc Nephrol. 2006. PMID: 16762990 Free article.
Thrombotic microangiopathies: thrombotic thrombocytopenic purpura / hemolytic uremic syndrome.
Polito MG, Kirsztajn GM. Polito MG, et al. J Bras Nefrol. 2010 Jul-Sep;32(3):303-15. J Bras Nefrol. 2010. PMID: 21103695 Free article.
Atypical hemolytic uremic syndrome.
Kavanagh D, Goodship TH, Richards A. Kavanagh D, et al. Semin Nephrol. 2013 Nov;33(6):508-30. doi: 10.1016/j.semnephrol.2013.08.003. Semin Nephrol. 2013. PMID: 24161037 Free PMC article. Review.
[Atypical HUS caused by complement-related abnormalities].
Yoshida Y, Matsumoto M. Yoshida Y, et al. Rinsho Ketsueki. 2015 Feb;56(2):185-93. doi: 10.11406/rinketsu.56.185. Rinsho Ketsueki. 2015. PMID: 25765799 Review. Japanese.
Two patients with history of STEC-HUS, posttransplant recurrence and complement gene mutations.
Alberti M, Valoti E, Piras R, Bresin E, Galbusera M, Tripodo C, Thaiss F, Remuzzi G, Noris M. Alberti M, et al. Am J Transplant. 2013 Aug;13(8):2201-6. doi: 10.1111/ajt.12297. Epub 2013 Jun 3. Am J Transplant. 2013. PMID: 23731345 Free article.
919 results
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