Human Genome Epidemiology Literature Finder
|
Records 1 - 11 (of 11 Records) |
| Query Trace: Proteinuria and WT1[original query] |
|---|
| Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome. Kidney international 2004 Aug 66 (2): 564-70. Ruf Rainer G, Schultheiss Michael, Lichtenberger Anne, Karle Stephanie M, Zalewski Isabella, Mucha Bettina, Everding Anne Schulze, Neuhaus Thomas, Patzer Ludwig, Plank Christian, Haas Johannes P, Ozaltin Fatih, Imm Anita, Fuchshuber Arno, Bakkaloglu Aysin, Hildebrandt Friedhelm, |
| Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9. Pediatric research 2006 Feb 59 (2): 325-31. Mucha Bettina, Ozaltin Fatih, Hinkes Bernward G, Hasselbacher Katrin, Ruf Rainer G, Schultheiss Michael, Hangan Daniela, Hoskins Bethan E, Everding Anne Schulze, Bogdanovic Radovan, Seeman Thomas, Hoppe Bernd, Hildebrandt Friedhelm, |
| Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1. Clinical journal of the American Society of Nephrology : CJASN 2015 May 10 (5): 825-31. Lehnhardt Anja, Karnatz Claartje, Ahlenstiel-Grunow Thurid, Benz Kerstin, Benz Marcus R, Budde Klemens, Büscher Anja K, Fehr Thomas, Feldkötter Markus, Graf Norbert, Höcker Britta, Jungraithmayr Therese, Klaus Günter, Koehler Birgit, Konrad Martin, Kranz Birgitta, Montoya Carmen R, Müller Dominik, Neuhaus Thomas J, Oh Jun, Pape Lars, Pohl Martin, Royer-Pokora Brigitte, Querfeld Uwe, Schneppenheim Reinhard, Staude Hagen, Spartà Giuseppina, Timmermann Kirsten, Wilkening Frauke, Wygoda Simone, Bergmann Carsten, Kemper Markus |
| Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome. Clinical journal of the American Society of Nephrology : CJASN 2015 Dec . Büscher Anja K, Beck Bodo B, Melk Anette, Hoefele Julia, Kranz Birgitta, Bamborschke Daniel, Baig Sabrina, Lange-Sperandio Bärbel, Jungraithmayr Theresa, Weber Lutz T, Kemper Markus J, Tönshoff Burkhard, Hoyer Peter F, Konrad Martin, Weber Stefanie, |
| Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome. Pediatric nephrology (Berlin, Germany) 2017 Feb . Wang Fang, Zhang Yanqin, Mao Jianhua, Yu Zihua, Yi Zhuwen, Yu Li, Sun Jun, Wei Xiuxiu, Ding Fangrui, Zhang Hongwen, Xiao Huijie, Yao Yong, Tan Weizhen, Lovric Svjetlana, Ding Jie, Hildebrandt Friedhe |
| Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome. BMC nephrology 2018 12 19 (1): 382. Li Guo-Min, Cao Qi, Shen Qian, Sun Li, Zhai Yi-Hui, Liu Hai-Mei, An Yu, Xu Ho |
| Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohort. European journal of medical genetics 2020 9 63 (11): 104047. Sun Shuzhen, Xu Linan, Bi Yunli, Wang Jing, Zhang Zhiqing, Tang Xiaoshan, Cao Qi, Zhai Yihui, Chen Jing, Fang Xiaoyan, Liu Jialu, Fang Ye, Xiang Tianchao, Qian Yanyan, Wu Bingbing, Wang Huijun, Zhou Wenhao, Shen Jian, Dong Kuiran, Liu Xiaorong, Zheng Bixia, Zhang Aihua, Wang Xiaowen, Wu Yubing, Ma Duan, Shen Qian, Rao Jia, Xu Ho |
| Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis. Journal of clinical medicine 2020 7 9 (6): . Park Eujin, Lee Chung, Kim Nayoung K D, Ahn Yo Han, Park Young Seo, Lee Joo Hoon, Kim Seong Heon, Cho Min Hyun, Cho Heeyeon, Yoo Kee Hwan, Shin Jae Il, Kang Hee Gyung, Ha Il-Soo, Park Woong-Yang, Cheong Hae |
| Mutational landscape of TRPC6, WT1, LMX1B, APOL1, PTPRO, PMM2, LAMB2 and WT1 genes associated with Steroid resistant nephrotic syndrome. Molecular biology reports 2021 Sep . Thakor Jinal M, Parmar Glory, Mistry Kinnari N, Gang Sishir, Rank Dharamshibhai N, Joshi Chaitanya |
| WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease. Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation 2021 8 16 (1): 46-54. Ferrari Maria T M, Watanabe Andreia, da Silva Thatiane E, Gomes Nathalia L, Batista Rafael L, Nishi Mirian Y, de Paula Leila C P, Costa Eduardo C, Costa Elaine M F, Cukier Priscilla, Onuchic Luiz F, Mendonca Berenice B, Domenice Sorah |
| 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 |
- Page last reviewed:Feb 1, 2024
- Content source: