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

Year Number of Results
1973 1
1980 1
1981 1
1986 1
1988 1
1989 2
1990 1
1993 1
1994 2
1995 4
1996 2
1997 1
1998 5
1999 4
2000 3
2001 9
2002 6
2003 7
2004 7
2005 5
2006 3
2007 3
2008 4
2009 7
2010 8
2011 6
2012 4
2013 3
2014 3
2015 4
2016 5
2018 1
2019 3
2021 2
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Similar articles for PMID: 10215327

114 results
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Page 1
Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura.
Noris M, Ruggenenti P, Perna A, Orisio S, Caprioli J, Skerka C, Vasile B, Zipfel PF, Remuzzi G. Noris M, et al. J Am Soc Nephrol. 1999 Feb;10(2):281-93. doi: 10.1681/ASN.V102281. J Am Soc Nephrol. 1999. PMID: 10215327 Free article.
Increased fragmentation of von Willebrand factor, due to abnormal cleavage of the subunit, parallels disease activity in recurrent hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and discloses predisposition in families. The Italian Registry of Familial and Recurrent HUS/TTP.
Galbusera M, Noris M, Rossi C, Orisio S, Caprioli J, Ruggeri ZM, Amadei B, Ruggenenti P, Vasile B, Casari G, Remuzzi G. Galbusera M, et al. Blood. 1999 Jul 15;94(2):610-20. Blood. 1999. PMID: 10397728 Free article.
Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.
Caprioli J, Castelletti F, Bucchioni S, Bettinaglio P, Bresin E, Pianetti G, Gamba S, Brioschi S, Daina E, Remuzzi G, Noris M; International Registry of Recurrent and Familial HUS/TTP. Caprioli J, et al. Hum Mol Genet. 2003 Dec 15;12(24):3385-95. doi: 10.1093/hmg/ddg363. Epub 2003 Oct 28. Hum Mol Genet. 2003. PMID: 14583443
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
114 results
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