Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 18 (of 18 Records) |
Query Trace: Membranoproliferative Glomerulonephritis[original query] |
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Two subtypes of hepatitis B virus-associated glomerulonephritis are associated with different HLA-DR2 alleles in Koreans. Tissue antigens 2003 Dec 62 (6): 505-11. Park M H, Song E Y, Ahn C, Oh K-H, Yang J, Kang S J, Lee H |
Is paraoxonase 192 gene polymorphism a risk factor for membranoproliferative glomerulonephritis in children? Cell biochemistry and function 0 25 (2): 159-65. Bilge Ilmay, Sirin Aydan, Agachan Bedia, Emre Sevinc, Sadikoglu Banu, Yilmaz Hülya, Sucu Aysegül, Isbir Turg |
Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease). Journal of medical genetics 2006 Jul 43 (7): 582-9. Abrera-Abeleda M A, Nishimura C, Smith J L H, Sethi S, McRae J L, Murphy B F, Silvestri G, Skerka C, Józsi M, Zipfel P F, Hageman G S, Smith R J |
Polymorphism of the FcgammaRIIalpha IgG receptor in patients with lupus nephritis and glomerulopathy. The Journal of rheumatology 2006 Mar 33 (3): 523-30. Gelmetti Adriana Peixoto, Freitas Antônio Carlos, Woronik Viktoria, Barros Rui Toledo, Bonfá Eloísa, Monteiro Renato Cos |
Complement factor H polymorphism p.Tyr402His and cuticular Drusen. Archives of ophthalmology (Chicago, Ill. : 1960) 2007 Jan 125 (1): 93-7. Grassi Michael A, Folk James C, Scheetz Todd E, Taylor Christine M, Sheffield Val C, Stone Edwin |
Complement factor H polymorphisms, renal phenotypes and age-related macular degeneration: the Blue Mountains Eye Study. Genes and immunity 2008 Apr 9 (3): 231-9. Xing C, Sivakumaran T A, Wang J J, Rochtchina E, Joshi T, Smith W, Mitchell P, Iyengar S |
Paraoxonase 1 polymorphisms in patients with primary glomerulonephritis: a single-center study in Turkey. Iranian journal of kidney diseases 2012 May 6 (3): 181-5. Eren Zehra, Kantarci Gulcin, Biyikli Nese, Arikan Hakki, Tuglular Serhan, Ergen Arzu, Isbir Turgay, Akoglu Em |
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 |
C3 glomerulonephritis and autoimmune disease: more than a fortuitous association? Journal of nephrology 2015 Jul . Alexander Mariam P, Fervenza Fernando C, De Vriese An S, Smith Richard J H, Nasr Samih H, Cornell Lynn D, Herrera Hernandez Loren P, Zhang Yuzhou, Sethi Sanje |
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 |
The role of MEFV mutations in the concurrent disorders observed in patients with familial Mediterranean fever. European journal of rheumatology 2016 Sep 3 (3): 118-121. Güncan Sabri, Bilge N ?ule Y, Cansu Döndü Üsküdar, Ka?ifo?lu Timuçin, Korkmaz Ceng |
Outcome of membranoproliferative glomerulonephritis and C3-glomerulopathy in children and adolescents. Pediatric nephrology (Berlin, Germany) 2018 9 33 (12): 2289-2298. Holle Johannes, Berenberg-Goßler Lena, Wu Kaiyin, Beringer Ortraud, Kropp Florian, Müller Dominik, Thumfart Jul |
Lack of Evidence for an Association between Previous HEV Genotype-3 Exposure and Glomerulonephritis in General. Pathogens (Basel, Switzerland) 2022 1 11 (1): . Pischke Sven, Tamanaei Sarah, Mader Maria, Schulze Zur Wiesch Julian, Petersen-Benz Christine, Haddad Munif, Addo Marylyn M, Schmidt Tilman, Huber Tobias B, Krebs Christian F, Steinmetz Oliver M, Turner Jan E, Hoxha Elion, Horvatits Thom |
Genetic investigation of Nordic patients with complement-mediated kidney diseases. Frontiers in immunology 2023 9 14 1254759. Viktor Rydberg, Sigridur Sunna Aradottir, Ann-Charlotte Kristoffersson, Naila Svitacheva, Diana Karpm |
The Association of Class I and II Human Leukocyte Antigen Serotypes With End-Stage Kidney Disease Due to Membranoproliferative Glomerulonephritis and Dense Deposit Disease. American journal of kidney diseases : the official journal of the National Kidney Foundation 2023 9 . Halimat Afolabi, Bing M Zhang, Michelle O'Shaughnessy, Glenn M Chertow, Richard Lafayette, Vivek Cha |
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 |
Anti-factor B antibodies in atypical hemolytic uremic syndrome. Pediatric nephrology (Berlin, Germany) 2024 1 . Priyanka Khandelwal, Shreesha Nambiar, Rahul Saini, Savita Saini, Poonam Coshic, Aditi Sinha, Pankaj Hari, Jayanth Kumar Palanichamy, Arvind Bag |
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- Page last updated:May 20, 2024
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