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HUS and TTP in Children.
Trachtman H. Trachtman H. Pediatr Clin North Am. 2013 Dec;60(6):1513-26. doi: 10.1016/j.pcl.2013.08.007. Pediatr Clin North Am. 2013. PMID: 24237985 Free PMC article. Review.
Drugs and trials: lessons from Plato.
Trachtman H. Trachtman H. Clin Ther. 2013 May;35(5):688-91. doi: 10.1016/j.clinthera.2013.03.018. Epub 2013 Apr 13. Clin Ther. 2013. PMID: 23587607 Free PMC article. No abstract available.
Mutations in FN1 cause glomerulopathy with fibronectin deposits.
Castelletti F, Donadelli R, Banterla F, Hildebrandt F, Zipfel PF, Bresin E, Otto E, Skerka C, Renieri A, Todeschini M, Caprioli J, Caruso RM, Artuso R, Remuzzi G, Noris M. Castelletti F, et al. Proc Natl Acad Sci U S A. 2008 Feb 19;105(7):2538-43. doi: 10.1073/pnas.0707730105. Epub 2008 Feb 11. Proc Natl Acad Sci U S A. 2008. PMID: 18268355 Free PMC article.
Thrombomodulin mutations in atypical hemolytic-uremic syndrome.
Delvaeye M, Noris M, De Vriese A, Esmon CT, Esmon NL, Ferrell G, Del-Favero J, Plaisance S, Claes B, Lambrechts D, Zoja C, Remuzzi G, Conway EM. Delvaeye M, et al. N Engl J Med. 2009 Jul 23;361(4):345-57. doi: 10.1056/NEJMoa0810739. N Engl J Med. 2009. PMID: 19625716 Free PMC article.
The complement factor H R1210C mutation is associated with atypical hemolytic uremic syndrome.
Martinez-Barricarte R, Pianetti G, Gautard R, Misselwitz J, Strain L, Fremeaux-Bacchi V, Skerka C, Zipfel PF, Goodship T, Noris M, Remuzzi G, de Cordoba SR; European Working Party on the Genetics of HUS. Martinez-Barricarte R, et al. J Am Soc Nephrol. 2008 Mar;19(3):639-46. doi: 10.1681/ASN.2007080923. Epub 2008 Jan 30. J Am Soc Nephrol. 2008. PMID: 18235085 Free PMC article.