Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 30 (of 199 Records) |
Query Trace: Glomerulonephritis[original query] |
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Phenotypic spectrum and antialbuminuric response to angiotensin converting enzyme inhibitor and angiotensin receptor blocker therapy in pediatric Dent disease. Molecular genetics & genomic medicine 2020 6 8 (8): e1306. Deng Haiyue, Zhang Yanqin, Xiao Huijie, Yao Yong, Zhang Hongwen, Liu Xiaoyu, Su Baige, Guan Na, Zhong Xuhui, Wang Suxia, Ding Jie, Wang Fa |
The telomerase gene polymorphisms, but not telomere length, increase susceptibility to primary glomerulonephritis/end stage renal diseases in females. Journal of translational medicine 2020 May 18 (1): 184. Sun Qing, Liu Junli, Cheng Guanghui, Dai Mingkai, Liu Jiaxi, Qi Zhenqiang, Zhao Jingjie, Li Wei, Kong Feng, Liu Gang, Björkholm Magnus, Xu Daw |
Genetic variants of the MIR31HG gene are related to a risk of IgA nephropathy. International immunopharmacology 2020 Apr 84 106533. Yuan Haozheng, Li Siyuan, Wang Li, Zhao Xijuan, Xue Li, Lei Xiaoming, Fu Rongg |
Clinicopathological Assessment of Kidney Biopsies in Children with Familial Mediterranean Fever: A Single-Center Experience. Nephron 2020 3 144 (5): 222-227. Yaz?l?ta? Fatma, Çak?c? Evrim Karg?n, Kurt ?ükür Eda Didem, Özdel Semanur, Arda Nilüfer, Güngör Tülin, Bülbül Mehm |
Genetic polymorphism in C3 is associated with progression in chronic kidney disease (CKD) patients with IgA nephropathy but not in other causes of CKD. PloS one 2020 15 (1): e0228101. Ibrahim Sara T, Chinnadurai Rajkumar, Ali Ibrahim, Payne Debbie, Rice Gillian I, Newman William G, Algohary Eman, Adam Ahmed G, Kalra Philip |
Novel pathogenic OCRL mutations and genotype-phenotype analysis of Chinese children affected by oculocerebrorenal syndrome: two cases and a literature review. BMC medical genomics 2021 9 14 (1): 219. Zhang Yu, Deng Linxia, Chen Xiaohong, Hu Yingjie, Chen Yaxian, Chen Kang, Zhou Jianh |
Association of Immune and Inflammatory Gene Polymorphism With the Risk of IgA Nephropathy: A Systematic Review and Meta-Analysis of 45 Studies. Frontiers in immunology 2021 12 683913. Ding Xiaonan, Mei Yan, Mao Zhi, Long Lingling, Han Qiuxia, You Yanqin, Zhu Han |
Paraoxonase 1 gene (PON1) variants concerning hepatitis C virus (HCV) spontaneous clearance in hemodialysis individuals: a case-control study. BMC infectious diseases 2021 8 21 (1): 875. Grzegorzewska Alicja E, Mostowska Adrianna, Warcho? Wojciech, Jagodzi?ski Pawe? |
Identification of a Locus on the X Chromosome Linked to Familial Membranous Nephropathy. Kidney international reports 2021 Jun 6 (6): 1669-1676. Downie Mallory L, Gupta Sanjana, Tekman Mehmet C, Cheshire Chris, Arora Steven, Licht Christoph, Robinson Lisa A, Munoz Marina, Aris Alvaro Madrid, Al Attrach Ibrahim, Brenchley Paul E, Gale Daniel P, Stanescu Horia, Bockenhauer Detlef, Kleta Robe |
Positive renal familial history in IgA nephropathy is associated with worse renal outcomes: a single-center longitudinal study. BMC nephrology 2021 6 22 (1): 230. Sato Yoshinori, Tsukaguchi Hiroyasu, Higasa Koichiro, Kawata Naoto, Inui Kiyoko, Linh Tran Nguyen Truc, Quynh Tran Thuy Huong, Yoshihiko Inoue, Koiwa Fumihiko, Yoshimura Ash |
New susceptible locus, rs9428555, is associated with pediatric-onset immunoglobulin A nephropathy and immunoglobulin A vasculitis in Koreans. Genes & genomics 2021 Jun . Lee Minho, Lee Gunhee, Kang Hee Gyung, Suh Jin-So |
Glucocorticoids Induce Partial Remission of Focal Segmental Glomerulosclerosis but Not Interstitial Nephritis in COVID-19 Acute Kidney Injury in an APOL1 Low-Risk Genotype White Patient. The American journal of case reports 2021 11 22 e933462. Nowak Piotr J, Forycka Joanna, Cegielska Natalia, Harendarz Karolina, W?growska-Danilewicz Ma?gorzata, Danilewicz Marian, P?oszaj Tomasz, Borowiec Maciej, Wlaze? Rafa?, Nowicki Mich |
The contribution of the LOC105371267 and MRPS30-DT genetic polymorphisms to IgA nephropathy in the Chinese Han population. American journal of translational research 2021 11 13 (10): 11718-11727. Chen Xiaoyan, Li Haiyue, Liu Yuanwei, Liu Jianfeng, Sun Yao, Wu Jiamin, Xiong Zichao, Cao W |
Case Report: A Pathogenic Missense Variant of WT1 Cosegregates With Proteinuria in a Six-Generation Chinese Family With IgA Nephropathy. Frontiers in medicine 2022 2 8 810940. Li Qianqian, Zhu Li, Shi Sufang, Xu Damin, Lv Jicheng, Zhang Ho |
Downregulation-resistant STAT4 risk haplotype contributes to lupus nephritis through CD4 T cell IFN-? production. Arthritis & rheumatology (Hoboken, N.J.) 2022 12 . Madera-Salcedo Iris K, Ramírez-Sánchez Ada L, Rodríguez-Rodríguez Noé, García-Quintero Roberto, Rubio Rosa M, de Oca Gabriela Morales-Montes, Dávalos Emmanuel, Cuervo Rogelio, Furuzawa-Carballeda Janette, Alcocer-Varela Jorge, Gómez-Martín Diana, González-Yáñez Marysol, de la Cruz Abigail, Albarrán-Godínez Adrián, Suárez-Rojas Gerardo, Romero-Díaz Juanita, Uribe-Uribe Norma O, Alarcón-Riquelme Marta, Furlan-Magaril Mayra, Mejía-Vilet Juan Manuel, Crispín José C, Rosetti Florenc |
Long-term kidney outcome of patients with rheumatological diseases and antineutrophil cytoplasmic antibody-glomerulonephritis: comparison with a primitive ANCA-glomerulonephritis cohort. Clinical and experimental rheumatology 2022 12 . Locatelli Laura, Calatroni Marta, Reggiani Francesco, Bonelli Grazia Dea, Gerosa Maria, Argolini Lorenza Maria, Trezzi Barbara, Del Papa Nicoletta, Angelini Claudio, Pozzi Maria Rosa, Sinico Renato Alberto, Moroni Gabriel |
Role of fluid-phase complement system regulation in the development of hepatitis C virus-associated glomerulonephritis. PloS one 2022 17 (10): e0276017. Ibrahim Sara T, Abdelhamid Marwa R, Lewis Neveen, Baddour Nahed, Adam Ahmed |
Genetic analysis of CFH and MCP in Egyptian patients with immune-complex proliferative glomerulonephritis. Frontiers in immunology 2022 10 13 960068. Gouda Heba R, Talaat Iman M, Bouzid Amal, El-Assi Hoda, Nabil Amira, Venkatachalam Thenmozhi, Manasa Bhamidimarri Poorna, Wohlers Inken, Mahdami Amena, El-Gendi Saba, ElKoraie Ahmed, Busch Hauke, Saber-Ayad Maha, Hamoudi Rifat, Baddour Nah |
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 |
Interleukin-6 and Epidermal Growth Factor as non-invasive biomarkers of progression in chronic glomerulonephritis. American journal of physiology. Cell physiology 2023 9 . Ilona Idasiak-Piechocka, Mi?osz Miedziaszczyk, Aldona Wo?niak, El?bieta Pawliczak, El?bieta Kaczmarek, Andrzej O |
Mesangial C3 Deposition, Complement-Associated Variant, and Disease Progression in IgA Nephropathy. Clinical journal of the American Society of Nephrology : CJASN 2023 8 . Yuqi Kang, Boyang Xu, Sufang Shi, Xujie Zhou, Pei Chen, Lijun Liu, Yebei Li, Yueqi Leng, Jicheng Lv, Li Zhu, Hong Zha |
[Genetic analysis of a patient with Alport syndrome due to compound heterozygous variants of COL4A4 gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 8 40 (9): 1150-1154. Bingbing Yang, Fengxun Liu, Lanlan Zou, Xiaoling Xue, Jinhong Mi |
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 |
Characteristics and outcome of ANCA-associated vasculitides induced by anti-thyroid drugs: a multicenter retrospective case-control study. Rheumatology (Oxford, England) 2023 6 . Julien Culerrier, Yann Nguyen, Omer Karadag, Sule Yasar Bilge, Tuba Demirci Yildrim, Tahir Saygin Ögüt, Veli Yazisiz, Cemal Bes, Ayse Celfe, Ayten Yazici, Oznur Sadioglu Cagdas, Andreas Kronbichler, David Jayne, Philipp Gauckler, Alexis Regent, Vitor Teixeira, Sylvain Marchand-Adam, Pierre Duffau, Saskia Ingen-Housz-Oro, Celine Droumaguet, Baptiste Andre, Luminita Luca, Sarah Lechtman, Achille Aouba, Celine Lebas, Amélie Servettaz, Amandine Dernoncourt, Marc Ruivard, Anne-Marie Milesi, Vincent Poindron, Patrick Jego, Roberto Padoan, Paolo Delvino, Frédéric Vandergheynst, Christian Pagnoux, Elaine Yacyshyn, Peter Lamprecht, Oliver Flossmann, Xavier Puéchal, Benjamin Terri |
Complement alternative pathway determines disease susceptibility and severity in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. Kidney international 2023 11 . Laura Lucientes-Continente, Gema Fernández-Juárez, Bárbara Márquez-Tirado, Laura Jiménez-Villegas, Mercedes Acevedo, Teresa Cavero, Luís Sánchez Cámara, Juliana Draibe, Paula Anton-Pampols, Fernando Caravaca-Fontán, Manuel Praga, Javier Villacorta, Elena Goicoechea de Jor |
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 |
Evaluation of the significance of complement-related genes mutations in atypical postinfectious glomerulonephritis: a pilot study. International urology and nephrology 2023 10 . Feng Xu, Changming Zhang, Mingchao Zhang, Xiaodong Zhu, Shuiqin Cheng, Zhen Cheng, Caihong Zeng, Song Jia |
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:Apr 16, 2024
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