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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 3, 2023. (Total: 223614Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Nephrotic Syndrome and EGFR[original query]
The association of podocin R229Q polymorphism with increased albuminuria or reduced estimated GFR in a large population-based sample of US adults.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2008 Nov 52 (5): 868-75.
Köttgen Anna, Hsu Charles C, Coresh Josef, Shuldiner Alan R, Berthier-Schaad Yvette, Gambhir Tejal Rami, Smith Michael W, Boerwinkle Eric, Kao W H Lin
Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects.
Journal of the American Society of Nephrology : JASN 2015 Jul .
Sampson Matthew G, Robertson Catherine C, Martini Sebastian, Mariani Laura H, Lemley Kevin V, Gillies Christopher E, Otto Edgar A, Kopp Jeffrey B, Randolph Anne, Vega-Warner Virginia, Eichinger Felix, Nair Viji, Gipson Debbie S, Cattran Daniel C, Johnstone Duncan B, O'Toole John F, Bagnasco Serena M, Song Peter X, Barisoni Laura, Troost Jonathan P, Kretzler Matthias, Sedor John R,
APOL1-associated glomerular disease among African-American children: a collaboration of the Chronic Kidney Disease in Children (CKiD) and Nephrotic Syndrome Study Network (NEPTUNE) cohorts.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2016 Apr .
Ng Derek K, Robertson Catherine C, Woroniecki Robert P, Limou Sophie, Gillies Christopher E, Reidy Kimberly J, Winkler Cheryl A, Hingorani Sangeeta, Gibson Keisha L, Hjorten Rebecca, Sethna Christine B, Kopp Jeffrey B, Moxey-Mims Marva, Furth Susan L, Warady Bradley A, Kretzler Matthias, Sedor John R, Kaskel Frederick J, Sampson Matthew
Timing of renal replacement therapy does not influence survival and growth in children with congenital nephrotic syndrome caused by mutations in NPHS1: data from the ESPN/ERA-EDTA Registry.
Pediatric nephrology (Berlin, Germany) 2016 Oct .
Hölttä Tuula, Bonthuis Marjolein, Van Stralen Karlijn J, Bjerre Anna, Topaloglu Rezan, Ozaltin Fatih, Holmberg Christer, Harambat Jerome, Jager Kitty J, Schaefer Franz, Groothoff Jaap
APOL1 risk genotype in Europe: Data in patients with focal segmental glomerulosclerosis and after renal transplantation.
Nephrologie & therapeutique 2019 Apr 15 Suppl 1 S85-S89.
Servais Aude, Gribouval Olivier, Gaillard François, Antignac Corin
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
A randomised controlled unblinded multicentre non-inferiority trial with activated vitamin D and prednisolone treatment in patients with minimal change nephropathy (ADAPTinMCN).
Trials 2021 7 22 (1): 442.
Kristensen Tilde, Birn Henrik, Ivarsen P
APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses.
Pediatric nephrology (Berlin, Germany) 2021 2 36 (8): 2327-2336.
Watanabe Andreia, Guaragna Mara Sanches, Belangero Vera Maria Santoro, Casimiro Fernanda Maria Serafim, Pesquero João Bosco, de Santis Feltran Luciana, Palma Lilian Monteiro Pereira, Varela Patrícia, de Menezes Neves Precil Diego Miranda, Lerario Antonio Marcondes, de Souza Marcela Lopes, de Mello Maricilda Palandi, de Brito Lutaif Anna Cristina Gervásio, Ferrari Cassio Rodrigues, Sampson Matthew Gordon, Onuchic Luiz Fernando, Nogueira Paulo Cesar Ko
Clinicopathological Impact of Gene Polymorphism of Nephrin and Glucocorticoid Receptor Genes in Egyptian Children with Nonfamilial Nephrotic Syndrome.
Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia 0 32 (6): 1615-1627.
El-Refaey Ahmed M, Elsamanoudy Ayman Z, Elmorsy Zakarya, Gaber Eman, Sarhan Amr, Hammad Aymman, Zedan Mohamed M, Bakr Ashr
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