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

Year Number of Results
1975 1
1998 2
2001 3
2002 2
2003 2
2004 2
2005 3
2006 2
2007 2
2008 2
2009 4
2010 10
2011 6
2012 10
2013 9
2014 16
2015 16
2016 12
2017 18
2018 19
2019 15
2020 10
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Publication date

Similar Articles for PMID: 22802583

149 results
Results by year
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Page 1
Thrombotic microangiopathy and associated renal disorders.
Barbour T, Johnson S, Cohney S, Hughes P. Barbour T, et al. Nephrol Dial Transplant. 2012 Jul;27(7):2673-85. doi: 10.1093/ndt/gfs279. Nephrol Dial Transplant. 2012. PMID: 22802583 Free PMC article. Review.
Consensus opinion on diagnosis and management of thrombotic microangiopathy in Australia and New Zealand.
Fox LC, Cohney SJ, Kausman JY, Shortt J, Hughes PD, Wood EM, Isbel NM, de Malmanche T, Durkan A, Hissaria P, Blombery P, Barbour TD. Fox LC, et al. Nephrology (Carlton). 2018 Jun;23(6):507-517. doi: 10.1111/nep.13234. Nephrology (Carlton). 2018. PMID: 29419916 Review.
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.
Consensus opinion on diagnosis and management of thrombotic microangiopathy in Australia and New Zealand.
Fox LC, Cohney SJ, Kausman JY, Shortt J, Hughes PD, Wood EM, Isbel NM, de Malmanche T, Durkan A, Hissaria P, Blombery P, Barbour TD. Fox LC, et al. Intern Med J. 2018 Jun;48(6):624-636. doi: 10.1111/imj.13804. Intern Med J. 2018. PMID: 29582550 Review.
[Diagnosis and treatment of TMA based on Japanese clinical guides].
Wada H, Hasegawa K, Watanabe M. Wada H, et al. Rinsho Ketsueki. 2017;58(7):849-856. doi: 10.11406/rinketsu.58.849. Rinsho Ketsueki. 2017. PMID: 28781284 Japanese.
Aetiology and pathogenesis of thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome: the role of von Willebrand factor-cleaving protease.
Furlan M, Lämmle B. Furlan M, et al. Best Pract Res Clin Haematol. 2001 Jun;14(2):437-54. doi: 10.1053/beha.2001.0142. Best Pract Res Clin Haematol. 2001. PMID: 11686108 Review.
STEC-HUS, atypical HUS and TTP are all diseases of complement activation.
Noris M, Mescia F, Remuzzi G. Noris M, et al. Nat Rev Nephrol. 2012 Nov;8(11):622-33. doi: 10.1038/nrneph.2012.195. Epub 2012 Sep 18. Nat Rev Nephrol. 2012. PMID: 22986360 Review.
Relative incidence of thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome in clinically suspected cases of thrombotic microangiopathy.
Schönermarck U, Ries W, Schröppel B, Pape L, Dunaj-Kazmierowska M, Burst V, Mitzner S, Basara N, Starck M, Schmidbauer D, Mellmann A, Dittmer R, Jeglitsch M, Haas CS. Schönermarck U, et al. Clin Kidney J. 2019 Jun 18;13(2):208-216. doi: 10.1093/ckj/sfz066. eCollection 2020 Apr. Clin Kidney J. 2019. PMID: 32296526 Free PMC article.
Atypical hemolytic uremic syndrome: from diagnosis to treatment.
Franchini M. Franchini M. Clin Chem Lab Med. 2015 Oct;53(11):1679-88. doi: 10.1515/cclm-2015-0024. Clin Chem Lab Med. 2015. PMID: 25803082 Free article. Review.
The complex differential diagnosis between thrombotic thrombocytopenic purpura and the atypical hemolytic uremic syndrome: Laboratory weapons and their impact on treatment choice and monitoring.
Mannucci PM, Cugno M. Mannucci PM, et al. Thromb Res. 2015 Nov;136(5):851-4. doi: 10.1016/j.thromres.2015.09.007. Epub 2015 Sep 12. Thromb Res. 2015. PMID: 26386489 Review.
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