Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Recurrence and CFH[original query] |
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| Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration. Nature genetics 2006 Sep 38 (9): 1055-9. Maller Julian, George Sarah, Purcell Shaun, Fagerness Jes, Altshuler David, Daly Mark J, Seddon Johanna |
| 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, |
| Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background. Clinical journal of the American Society of Nephrology : CJASN 2006 Jan 1 (1): 88-99. Bresin Elena, Daina Erica, Noris Marina, Castelletti Federica, Stefanov Rumen, Hill Prudence, Goodship Timothy H J, Remuzzi Giuseppe, |
| Complement factor H and high-temperature requirement A-1 genotypes and treatment response of age-related macular degeneration. Ophthalmology 2011 Jan 118 (1): 93-100. Tsuchihashi Takashi, Mori Keisuke, Horie-Inoue Kuniko, Gehlbach Peter L, Kabasawa Sho, Takita Hiroyasu, Ueyama Kazuhiro, Okazaki Yasushi, Inoue Satoshi, Awata Takuya, Katayama Shigehiro, Yoneya Sh |
| Association of CFH and SERPING1 polymorphisms with anterior uveitis. The British journal of ophthalmology 2013 Nov 97 (11): 1475-80. Yang Ming-ming, Lai Timothy Y Y, Tam Pancy O S, Chiang Sylvia W Y, Ng Tsz Kin, Rong Shi Song, Pang Chi P |
| 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 |
| ARMS2 A69S polymorphism is associated with the number of ranibizumab injections needed for exudative age-related macular degeneration in a pro re nata regimen during 4 years of follow-up. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 2017 Jul . Valverde-Megías Alicia, Veganzones-de-Castro Silvia, Donate-López Juan, Maestro-de-Las-Casas Maria Luisa, Megías-Fresno Alicia, García-Feijoo Juli |
| Clinical Evaluation of BRCA1/2 Mutation in Mexican Ovarian Cancer Patients. Translational oncology 2019 Dec 13 (2): 212-220. Gallardo-Rincón Dolores, Álvarez-Gómez Rosa María, Montes-Servín Edgar, Toledo-Leyva Alfredo, Montes-Servín Elizabeth, Michel-Tello David, Alamilla-García Gabriela, Bahena-González Antonio, Hernández-Nava Elizabeth, Fragoso-Ontiveros Veronica, Espinosa-Romero Raquel, Cetina-Pérez Luce |
| Genetic factors associated with treatment response to reduced-fluence photodynamic therapy for chronic central serous chorioretinopathy. Molecular vision 2020 8 26 505-509. Hayashida Mayuka, Miki Akiko, Nakai Shunichiro, Matsumiya Wataru, Imai Hisanori, Kusuhara Sentaro, Honda Shigeru, Nakamura Mako |
| Genetic factors associated with response to as-needed aflibercept therapy for typical neovascular age-related macular degeneration and polypoidal choroidal vasculopathy. Scientific reports 2020 Apr 10 (1): 7188. Yoneyama Seigo, Sakurada Yoichi, Kikushima Wataru, Sugiyama Atsushi, Matsubara Mio, Fukuda Yoshiko, Tanabe Naohiko, Parikh Ravi, Mabuchi Fumihiko, Kashiwagi Kenji, Iijima Hiroyu |
| Genetic association with intravitreal ranibizumab response for neovascular age-related macular degeneration in Hispanic population. Taiwan journal of ophthalmology 0 9 (4): 243-248. Rodríguez Francisco Jose, Rios Hernan Andres, Aguilar María Camila, Rosenstiehl Shirley Margarita, Gelvez Nancy, Lopez Greizy, Tamayo Martha |
| CFH I62V as a Putative Genetic Marker for Posner-Schlossman Syndrome. Frontiers in immunology 2021 3 12 608723. Yang Ming Ming, Sun Hong Yan, Meng Ting, Qiu Shan Hu, Zeng Qi Qiao, Ng Tsz Kin, Jiang Li, Deng Ting Ming, Zeng Ai Neng, Wang Jun, Luo Xiao Li |
| Clinicopathologic Implications of Complement Genetic Variants in Kidney Transplantation. Frontiers in medicine 2021 12 8 775280. Ren Zhen, Perkins Stephen J, Love-Gregory Latisha, Atkinson John P, Java Anu |
| Rare Variants in Complement Gene in C3 Glomerulopathy and Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis. Clinical journal of the American Society of Nephrology : CJASN 2023 8 . Marie Sophie Meuleman, Paula Vieira Martins, Carine El Sissy, Vincent Audard, Véronique Baudouin, Dominique Bertrand, Frank Bridoux, Férielle Louillet, Claire Dossier, Vincent Esnault, Noémie Jourde-Chiche, Alexandre Karras, Marie-Pascale Morin, François Provot, Philippe Remy, David Ribes, Caroline Rousset-Rouviere, Aude Servais, Eric Thervet, Leila Tricot, Mohamad Zaidan, Alain Wynckel, Julien Zuber, Moglie Le Quintrec, Véronique Frémeaux-Bacchi, Sophie Chauv |
| Low C3 in a 4-month-old baby: is it a problem? Pediatric nephrology (Berlin, Germany) 2023 11 . Gül?ah Kaya Aksoy, Mustafa Gökhan Ertosun, Mustafa Koyun, Elif Çomak, Sema Akm |
| Association of KDR (rs2071559, rs1870377), CFH (rs1061170, rs1410996) genes variants and serum levels with pituitary adenoma. Molecular genetics & genomic medicine 2023 10 e2289. Akvile Bruzaite, Greta Gedvilaite, Loresa Kriauciuniene, Rasa Liutkevicie |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 01, 2023
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