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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Nov 3, 2024. (Total: 233167Documents)
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Records 1 - 10 (of 10 Records)

Query Trace: Mesangial Proliferative Glomerulonephritis[original query]
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
The influence of endothelin-A receptor gene polymorphism on the progression of autosomal dominant polycystic kidney disease and IgA nephropathy.
Folia biologica 2007 53 (4): 134-7.
Reiterová J, Merta M, Stekrová J, Maixnerová D, Obeidová H, Kebrdlová V, Viklický O, Tesar
Interleukin-6 gene polymorphism and faster progression to end-stage renal failure in chronic glomerulonephritis.
Translational research : the journal of laboratory and clinical medicine 2007 Aug 150 (2): 101-5.
Buraczynska Monika, Jozwiak Lucyna, Ksiazek Piotr, Borowicz Ewa, Mierzicki Pio
Impact of the -675 4G/5G polymorphism of the plasminogen activator inhibitor-1 gene on childhood IgA nephropathy.
Experimental and therapeutic medicine 2012 Apr 3 (4): 703-706.
Han Su-Ryun, Kim Cheon-Jong, Lee Byung-Che
Complement factor H gene associations with end-stage kidney disease in African Americans.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2014 Jul 29 (7): 1409-14.
Bonomo Jason A, Palmer Nicholette D, Hicks Pamela J, Lea Janice P, Okusa Mark D, Langefeld Carl D, Bowden Donald W, Freedman Barry
Association of human leukocyte antigen gene polymorphism and mesangial proliferative glomerulonephritis in a large population-based study.
Biomedical reports 2013 Sep 1 (5): 751-756.
Zhao Jing-Jie, Wang Xi-Bing, Luan Yun, Liu Jun-Li, Liu Ling, Jia Hong-Yi
Angiotensin-converting enzyme genotype is not a significant genetic risk factor for idiopathic nephrotic syndrome in Croatian children.
Nephron 2015 130 (1): 29-34.
Batini? Danko, Serti? Jadranka, ?ori? Marijana, Konjevoda Paško, Batini? Danica, Miloševi? Dan
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
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
[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
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