HuGE Literature Finder
Records
1
-
8
| Complement Gene Variants and Shiga Toxin-Producing Escherichia coli-Associated Hemolytic Uremic Syndrome: Retrospective Genetic and Clinical Study. 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 |
| 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 |
| 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 |
| Complement mutations in diacylglycerol kinase-e-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 |
| 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 |
| 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, |
| 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 |
| 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 |
- Page last reviewed:Oct 1, 2021
- Page last updated:Jun 28, 2022
- Content source: