Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Public Health Genomics and Precision Health Knowledge Base (v6.2)

Note: Javascript is disabled or is not supported by your browser. For this reason, some items on this page will be unavailable. For more information about this message, please visit this page: About CDC.gov.

HuGE Navigator|HuGE Literature Finder|PHGKB

HuGE Literature Finder

Records 1-13

Query Trace: Hemolytic-Uremic Syndrome and C3[orginal query]

Complement Gene Variants and Shiga Toxin-Producing Clinical journal of the American Society of Nephrology : CJASN 2019 Jan . Frémeaux-Bacchi Véronique, Sellier-Leclerc Anne-Laure, Vieira-Martins Paula, Limou Sophie, Kwon Theresa, Lahoche Annie, Novo Robert, Llanas Brigitte, Nobili François, Roussey Gwenaëlle, Cailliez Mathilde, Ulinski Tim, Deschênes Georges, Alberti Corinne, Weill François-Xavier, Mariani Patricia, Loirat Chant Similar articles in PubMed
Comprehensive Analysis of Complement Genes in Patients with Atypical Hemolytic Uremic Syndrome. American journal of nephrology 2016 Apr 43 (3): 160-169. Zhang Tao, Lu Jianping, Liang Shaoshan, Chen Dachen, Zhang Haitao, Zeng Caihong, Liu Zhihong, Chen Huim Similar articles in PubMed
A novel quantitative hemolytic assay coupled with restriction fragment length polymorphisms analysis enabled early diagnosis of atypical hemolytic uremic syndrome and identified unique predisposing mutations in Japan. PloS one 2015 10 (5): e0124655. Yoshida Yoko, Miyata Toshiyuki, Matsumoto Masanori, Shirotani-Ikejima Hiroko, Uchida Yumiko, Ohyama Yoshifumi, Kokubo Tetsuro, Fujimura Yoshihi Similar articles in PubMed
Complement mutations in diacylglycerol kinase-?-associated atypical hemolytic uremic syndrome. Clinical journal of the American Society of Nephrology : CJASN 2014 Sep 9 (9): 1611-9. Sánchez Chinchilla Daniel, Pinto Sheila, Hoppe Bernd, Adragna Marta, Lopez Laura, Justa Roldan Maria Luisa, Peña Antonia, Lopez Trascasa Margarita, Sánchez-Corral Pilar, Rodríguez de Córdoba Santia Similar articles in PubMed
Analysis of rare variants in the C3 gene in patients with age-related macular degeneration. PloS one 2014 9 (4): e94165. Duvvari Maheswara R, Paun Codrut C, Buitendijk Gabriëlle H S, Saksens Nicole T M, Volokhina Elena B, Ristau Tina, Schoenmaker-Koller Frederieke E, van de Ven Johannes P H, Groenewoud Joannes M M, van den Heuvel Lambertus P W J, Hofman Albert, Fauser Sascha, Uitterlinden André G, Klaver Caroline C W, Hoyng Carel B, de Jong Eiko K, den Hollander Anneke Similar articles in PubMed
Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome. American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2013 Mar 13 (3): 663-75. Le Quintrec M, Zuber J, Moulin B, Kamar N, Jablonski M, Lionet A, Chatelet V, Mousson C, Mourad G, Bridoux F, Cassuto E, Loirat C, Rondeau E, Delahousse M, Frémeaux-Bacchi Similar articles in PubMed
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype. Journal of the American Society of Nephrology : JASN 2013 Feb 24 (3): 475-86. Bresin Elena, Rurali Erica, Caprioli Jessica, Sanchez-Corral Pilar, Fremeaux-Bacchi Veronique, Rodriguez de Cordoba Santiago, Pinto Sheila, Goodship Timothy H J, Alberti Marta, Ribes David, Valoti Elisabetta, Remuzzi Giuseppe, Noris Marina, Similar articles in PubMed
Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS. Molecular immunology 2012 Jan 49 (4): 640-8. Ermini Luca, Goodship Timothy H J, Strain Lisa, Weale Michael E, Sacks Steven H, Cordell Heather J, Fremeaux-Bacchi Veronique, Sheerin Neil Similar articles in PubMed
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. Clinical journal of the American Society of Nephrology : CJASN 2010 Oct 5 (10): 1844-59. Noris Marina, Caprioli Jessica, Bresin Elena, Mossali Chiara, Pianetti Gaia, Gamba Sara, Daina Erica, Fenili Chiara, Castelletti Federica, Sorosina Annalisa, Piras Rossella, Donadelli Roberta, Maranta Ramona, van der Meer Irene, Conway Edward M, Zipfel Peter F, Goodship Timothy H, Remuzzi Giusep Similar articles in PubMed
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Human mutation 2010 Jun 31 (6): E1445-60. Maga Tara K, Nishimura Carla J, Weaver Amy E, Frees Kathy L, Smith Richard J Similar articles in PubMed
Thrombomodulin mutations in atypical hemolytic-uremic syndrome. The New England journal of medicine 2009 Jul 361 (4): 345-57. Delvaeye Mieke, Noris Marina, De Vriese Astrid, Esmon Charles T, Esmon Naomi L, Ferrell Gary, Del-Favero Jurgen, Plaisance Stephane, Claes Bart, Lambrechts Diether, Zoja Carla, Remuzzi Giuseppe, Conway Edward Similar articles in PubMed
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome. Blood 2006 Aug 108 (4): 1267-79. Caprioli Jessica, Noris Marina, Brioschi Simona, Pianetti Gaia, Castelletti Federica, Bettinaglio Paola, Mele Caterina, Bresin Elena, Cassis Linda, Gamba Sara, Porrati Francesca, Bucchioni Sara, Monteferrante Giuseppe, Fang Celia J, Liszewski M K, Kavanagh David, Atkinson John P, Remuzzi Giuseppe, Similar articles in PubMed
Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries. Journal of medical genetics 2003 Sep 40 (9): 676-81. Neumann H P H, Salzmann M, Bohnert-Iwan B, Mannuelian T, Skerka C, Lenk D, Bender B U, Cybulla M, Riegler P, Königsrainer A, Neyer U, Bock A, Widmer U, Male D A, Franke G, Zipfel P Similar articles in PubMed

File Formats Help:

How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?

Page last reviewed:Mar 16, 2019
Page last updated:Apr 02, 2020
Content source:

TOP