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

Year Number of Results
1991 1
1994 1
1995 1
1998 1
1999 5
2001 5
2002 3
2003 6
2004 4
2005 9
2006 13
2007 13
2008 2
2009 3
2010 11
2011 7
2012 4
2013 9
2014 5
2015 1
2016 3
2017 2
2018 2
2019 3
2020 1
2021 2
2022 4
2024 1

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Similar articles for PMID: 14615110

108 results

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Page 1
Familial haemolytic uraemic syndrome and an MCP mutation.
Noris M, Brioschi S, Caprioli J, Todeschini M, Bresin E, Porrati F, Gamba S, Remuzzi G; International Registry of Recurrent and Familial HUS/TTP. Noris M, et al. Lancet. 2003 Nov 8;362(9395):1542-7. doi: 10.1016/S0140-6736(03)14742-3. Lancet. 2003. PMID: 14615110
A rare pathogenic MCP mutation in patient with congenital TTP.
Masnic F, Resic H, Ajanovic S, Beciragic A, Prohic N. Masnic F, et al. Hematol Transfus Cell Ther. 2024 Jul-Sep;46(3):303-305. doi: 10.1016/j.htct.2022.01.009. Epub 2022 Feb 24. Hematol Transfus Cell Ther. 2024. PMID: 35305938 Free article. No abstract available.
Complement factor H: a guardian within?
Boudhabhay I, Roumenina LT. Boudhabhay I, et al. Kidney Int. 2021 Oct;100(4):747-749. doi: 10.1016/j.kint.2021.07.023. Kidney Int. 2021. PMID: 34556298
Complement Gene Variants and Shiga Toxin-Producing Escherichia coli-Associated Hemolytic Uremic Syndrome: Retrospective Genetic and Clinical Study.
Frémeaux-Bacchi V, Sellier-Leclerc AL, Vieira-Martins P, Limou S, Kwon T, Lahoche A, Novo R, Llanas B, Nobili F, Roussey G, Cailliez M, Ulinski T, Deschênes G, Alberti C, Weill FX, Mariani P, Loirat C. Frémeaux-Bacchi V, et al. Clin J Am Soc Nephrol. 2019 Mar 7;14(3):364-377. doi: 10.2215/CJN.05830518. Epub 2019 Jan 23. Clin J Am Soc Nephrol. 2019. PMID: 30674459 Free PMC article.
108 results