Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: Abnormalities and CFH[original query] |
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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 the bilaterality of age-related macular degeneration. Archives of ophthalmology (Chicago, Ill. : 1960) 2009 Oct 127 (10): 1339-44. Pai Amy Shih-I, Mitchell Paul, Rochtchina Elena, Iyengar Sudha, Wang Jie Jin, |
Is complement factor H a susceptibility factor for IgA nephropathy? Molecular immunology 2009 Apr 46 (7): 1405-8. Edey Matthew, Strain Lisa, Ward Roy, Ahmed Saeed, Thomas Trevor, Goodship Timothy H |
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 |
Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS). Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2010 Jul 25 (7): 2195-202. Westra Dineke, Volokhina Elena, van der Heijden Eefje, Vos Annemieke, Huigen Marleen, Jansen Jitske, van Kaauwen Edwin, van der Velden Thea, van de Kar Nicole, van den Heuvel Lambe |
Associations of complement factor H and smoking with early age-related macular degeneration: the ALIENOR study. Investigative ophthalmology & visual science 2011 Jul 52 (8): 5955-62. Delcourt Cécile, Delyfer Marie-Noëlle, Rougier Marie-Bénédicte, Amouyel Philippe, Colin Joseph, Le Goff Mélanie, Malet Florence, Dartigues Jean-François, Lambert Jean-Charles, Korobelnik Jean-Franço |
Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies. Kidney international 2012 Mar . Servais A, Noël LH, Roumenina LT, Le Quintrec M, Ngo S, Dragon-Durey MA, Macher MA, Zuber J, Karras A, Provot F, Moulin B, Grünfeld JP, Niaudet P, Lesavre P, Frémeaux-Bacchi V |
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, |
Long-term blood pressure and age-related macular degeneration: the ALIENOR study. Investigative ophthalmology & visual science 2013 Mar 54 (3): 1905-12. Cougnard-Grégoire Audrey, Delyfer Marie-Noëlle, Korobelnik Jean-François, Rougier Marie-Bénédicte, Malet Florence, Le Goff Mélanie, Dartigues Jean-François, Colin Joseph, Barberger-Gateau Pascale, Delcourt Céci |
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 |
Factors determining penetrance in familial atypical haemolytic uraemic syndrome. Journal of medical genetics 2014 Nov 51 (11): 756-64. Sansbury Francis H, Cordell Heather J, Bingham Coralie, Bromilow Gilly, Nicholls Anthony, Powell Roy, Shields Bev, Smyth Lucy, Warwicker Paul, Strain Lisa, Wilson Valerie, Goodship Judith A, Goodship Timothy H J, Turnpenny Peter |
Sunlight exposure, pigmentation, and incident age-related macular degeneration. Investigative ophthalmology & visual science 2014 Sep 55 (9): 5855-61. Klein Barbara E K, Howard Kerri P, Iyengar Sudha K, Sivakumaran Theru A, Meyers Kristin J, Cruickshanks Karen J, Klein Rona |
Chronic central serous chorioretinopathy is associated with genetic variants implicated in age-related macular degeneration. Ophthalmology 2015 Mar 122 (3): 562-70. de Jong Eiko K, Breukink Myrte B, Schellevis Rosa L, Bakker Bjorn, Mohr Jacqueline K, Fauser Sascha, Keunen Jan E E, Hoyng Carel B, den Hollander Anneke I, Boon Camiel J |
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 gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome. Molecular immunology 2016 Feb 71 131-142. Iatropoulos Paraskevas, Noris Marina, Mele Caterina, Piras Rossella, Valoti Elisabetta, Bresin Elena, Curreri Manuela, Mondo Elena, Zito Anna, Gamba Sara, Bettoni Serena, Murer Luisa, Fremeaux-Bacchi Veronique, Vivarelli Marina, Emma Francesco, Daina Erica, Remuzzi Giusep |
Factor H Competitor Generated by Gene Conversion Events Associates with Atypical Hemolytic Uremic Syndrome. Journal of the American Society of Nephrology : JASN 2017 10 29 (1): 240-249. Goicoechea de Jorge Elena, Tortajada Agustín, García Sheila Pinto, Gastoldi Sara, Merinero Héctor Martín, García-Fernández Jesús, Arjona Emilia, Cao Mercedes, Remuzzi Giuseppe, Noris Marina, Rodríguez de Córdoba Santia |
Clinical characteristics and genetic backgrounds of Japanese patients with atypical hemolytic uremic syndrome. Clinical and experimental nephrology 2018 3 22 (5): 1088-1099. Fujisawa Madoka, Kato Hideki, Yoshida Yoko, Usui Tomoko, Takata Munenori, Fujimoto Mika, Wada Hideo, Uchida Yumiko, Kokame Koichi, Matsumoto Masanori, Fujimura Yoshihiro, Miyata Toshiyuki, Nangaku Masao |
Major Predictive Factors for Progression of Early to Late Age-Related Macular Degeneration. Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde 2020 3 243 (6): 444-452. Sitnilska Vasilena, Kersten Eveline, Altay Lebriz, Schick Tina, Enders Philip, de Jong Eiko K, Langmann Thomas, Hoyng Carel B, den Hollander Anneke I, Fauser Sasc |
Pentosan polysulfate sodium (Elmiron) maculopathy: a genetic perspective. Retina (Philadelphia, Pa.) 2023 3 . Kalaw Fritz Gerald P, Ignacio John Carlos I, Wu Chris Y, Ferreyra Henry, Nudleman Eric, Baxter Sally L, Freeman William R, Borooah Shyaman |
Complement gene mutations in children with C3 glomerulopathy: do they affect the response to mycophenolate mofetil? Pediatric nephrology (Berlin, Germany) 2023 12 . Neslihan Günay, ?smail Dursun, ?brahim Gökçe, Mehtap Akbal?k Kara, Demet Tekcan, Neslihan Çiçek, Meral Torun Bayram, Mustafa Koyun, Nida Dinçel, Hasan Dursun, Seha Sayg?l?, Zeynep Nagehan Yürük Y?ld?r?m, Selçuk Yüksel, Osman Dönmez, Sibel Yel, Beltinge Demircio?lu K?l?ç, Özlem Aydo?, Bahriye Atm??, Aysun Çalt?k Y?lmaz, Sevcan A Bakkalo?lu, Mehmet Baha Aytaç, Mehmet Ta?demir, Belde Kasap Demir, Alper Soylu, Elif Çomak, Asl? Kantar Öz?ahin, Alper Kaçar, Nur Canpolat, Alev Y?lmaz, ?lknur Giri?gen, Kadirye Betül Akkoyunlu, Harika Alpay, Hakan M Poyrazo? |
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