These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
142 related articles for article (PubMed ID: 38231721)
1. Collapsing Glomerulopathy in a Patient with a TRPC6 Mutation Presenting as Rapidly Progressive Glomerulonephritis: A Case Report and Review of the Literature. Gokce I; Kaya M; Cicek N; Guven S; Ercetin Y; Yildiz N; Kaya H; Alpay H Saudi J Kidney Dis Transpl; 2023 May; 34(3):254-258. PubMed ID: 38231721 [TBL] [Abstract][Full Text] [Related]
2. Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa. Nandlal L; Winkler CA; Bhimma R; Cho S; Nelson GW; Haripershad S; Naicker T Eur J Pediatr; 2022 Oct; 181(10):3595-3606. PubMed ID: 35920919 [TBL] [Abstract][Full Text] [Related]
3. Heterozygous missense variant in TRPC6 in a boy with rapidly progressive infantile nephrotic syndrome associated with diffuse mesangial sclerosis. Hanafusa H; Hidaka Y; Yamaguchi T; Shimojo H; Tsukahara T; Murase T; Matsuoka D; Chiba N; Shimada S; Morokawa H; Omori N; Minoura H; Nagano C; Takano K; Nakamura K; Wakui K; Fukushima Y; Uehara T; Nakazawa Y; Iijima K; Nozu K; Kosho T Am J Med Genet A; 2021 Jul; 185(7):2175-2179. PubMed ID: 33884742 [TBL] [Abstract][Full Text] [Related]
4. Ocular manifestations of the genetic causes of focal and segmental glomerulosclerosis. Zhu V; Huang T; Wang D; Colville D; Mack H; Savige J Pediatr Nephrol; 2024 Mar; 39(3):655-679. PubMed ID: 37578539 [TBL] [Abstract][Full Text] [Related]
5. Genetic basis of nephrotic syndrome--review. Obeidová H; Merta M; Reiterová J; Maixnerová D; Stekrová J; Rysavá R; Tesar V Prague Med Rep; 2006; 107(1):5-16. PubMed ID: 16752799 [TBL] [Abstract][Full Text] [Related]
6. TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype. Gigante M; Caridi G; Montemurno E; Soccio M; d'Apolito M; Cerullo G; Aucella F; Schirinzi A; Emma F; Massella L; Messina G; De Palo T; Ranieri E; Ghiggeri GM; Gesualdo L Clin J Am Soc Nephrol; 2011 Jul; 6(7):1626-34. PubMed ID: 21734084 [TBL] [Abstract][Full Text] [Related]
7. [Four cases of nephrotic syndrome with TRPC6 gene variations and literature review]. Sun LW; Sun L; Wang P; Kang YL; Wu Y; Zhu GH; Huang WY Zhonghua Er Ke Za Zhi; 2021 Mar; 59(3):223-227. PubMed ID: 33657698 [No Abstract] [Full Text] [Related]
8. Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis. Löwik M; Levtchenko E; Westra D; Groenen P; Steenbergen E; Weening J; Lilien M; Monnens L; van den Heuvel L Nephrol Dial Transplant; 2008 Oct; 23(10):3146-51. PubMed ID: 18443213 [TBL] [Abstract][Full Text] [Related]
9. Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis. Büscher AK; Celebi N; Hoyer PF; Klein HG; Weber S; Hoefele J Pediatr Nephrol; 2018 Mar; 33(3):433-437. PubMed ID: 29038887 [TBL] [Abstract][Full Text] [Related]
10. Screening of ACTN4 and TRPC6 mutations in a Chinese cohort of patients with adult-onset familial focal segmental glomerulosclerosis. Zhang Q; Ma J; Xie J; Wang Z; Zhu B; Hao X; Yang L; Ren H; Chen N Contrib Nephrol; 2013; 181():91-100. PubMed ID: 23689571 [TBL] [Abstract][Full Text] [Related]
11. Novel gain-of-function mutation of TRPC6 Q134P contributes to late onset focal segmental glomerulosclerosis in a Chinese pedigree. Liu Z; Zhang H; Zhao S; Zhang Q; Zhang R; Han Y; Shao L; Zhao X Nephrology (Carlton); 2021 Dec; 26(12):1018-1025. PubMed ID: 34387384 [TBL] [Abstract][Full Text] [Related]
13. Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience. Bińczak-Kuleta A; Rubik J; Litwin M; Ryder M; Lewandowska K; Taryma-Leśniak O; Clark JS; Grenda R; Ciechanowicz A Bosn J Basic Med Sci; 2014 May; 14(2):89-93. PubMed ID: 24856380 [TBL] [Abstract][Full Text] [Related]
14. Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients. Büscher AK; Konrad M; Nagel M; Witzke O; Kribben A; Hoyer PF; Weber S Clin Nephrol; 2012 Jul; 78(1):47-53. PubMed ID: 22732337 [TBL] [Abstract][Full Text] [Related]
15. TRPC6 Mutational Analysis in Iranian Children With Focal Segmental Glomerulosclerosis. Gheissari A; Meamar R; Kheirollahi M; Rouigari M; Dehbashi M; Dehghani L; Abedini A Iran J Kidney Dis; 2018 Nov; 12(6):341-349. PubMed ID: 30595563 [TBL] [Abstract][Full Text] [Related]
16. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity. Bullich G; Trujillano D; Santín S; Ossowski S; Mendizábal S; Fraga G; Madrid Á; Ariceta G; Ballarín J; Torra R; Estivill X; Ars E Eur J Hum Genet; 2015 Sep; 23(9):1192-9. PubMed ID: 25407002 [TBL] [Abstract][Full Text] [Related]
17. TRPC6 and NPHS2 gene variants in adult patients with steroid-resistant nephrotic syndrome in North-West of Iran. Zununi Vahed S; Moghaddas Sani H; Haghi M; Mohajel Shoja M; Ardalan M Mol Biol Rep; 2019 Dec; 46(6):6339-6344. PubMed ID: 31529341 [TBL] [Abstract][Full Text] [Related]
18. Familial focal segmental glomerulosclerosis (FSGS) in a Nigerian family and exclusion of mutations in NPHS2,WT1 and APOL1. Anochie IC; Eke FU; Okpere AN West Afr J Med; 2012; 31(4):273-6. PubMed ID: 23468032 [TBL] [Abstract][Full Text] [Related]
19. Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis. Barua M; Brown EJ; Charoonratana VT; Genovese G; Sun H; Pollak MR Kidney Int; 2013 Feb; 83(2):316-22. PubMed ID: 23014460 [TBL] [Abstract][Full Text] [Related]