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.
6. Variations of type IV collagen-encoding genes in patients with histological diagnosis of focal segmental glomerulosclerosis. Demir E; Caliskan Y Pediatr Nephrol; 2020 Jun; 35(6):927-936. PubMed ID: 31254113 [TBL] [Abstract][Full Text] [Related]
7. Genetic mutational testing of Chinese children with familial hematuria with biopsy‑proven FSGS. Li Y; Wang Y; He Q; Dang X; Cao Y; Wu X; Mo S; He X; Yi Z Mol Med Rep; 2018 Jan; 17(1):1513-1526. PubMed ID: 29138824 [TBL] [Abstract][Full Text] [Related]
8. Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis. Gast C; Pengelly RJ; Lyon M; Bunyan DJ; Seaby EG; Graham N; Venkat-Raman G; Ennis S Nephrol Dial Transplant; 2016 Jun; 31(6):961-70. PubMed ID: 26346198 [TBL] [Abstract][Full Text] [Related]
9. Next-generation sequencing in patients with familial FSGS: first report of collagen gene mutations in Tunisian patients. Ammar S; Kanoun H; Kammoun K; Domingo-Gallego A; Ruiz P; Lorente-Grandoso L; Pybus M; Maalej B; Boudawara T; Kamoun H; Ben Hmida M; Ars E; Jarraya F J Hum Genet; 2021 Aug; 66(8):795-803. PubMed ID: 33654185 [TBL] [Abstract][Full Text] [Related]
10. Advances in molecular diagnosis and therapeutics in nephrotic syndrome and focal and segmental glomerulosclerosis. Sharif B; Barua M Curr Opin Nephrol Hypertens; 2018 May; 27(3):194-200. PubMed ID: 29465426 [TBL] [Abstract][Full Text] [Related]
11. A novel heterozygous variant of the COL4A4 gene in a Chinese family with hematuria and proteinuria leads to focal segmental glomerulosclerosis and chronic kidney disease. Fan LL; Liu L; Luo FM; Du R; Wang CY; Dong Y; Liu JS Mol Genet Genomic Med; 2020 Dec; 8(12):e1545. PubMed ID: 33159707 [TBL] [Abstract][Full Text] [Related]
12. Importance of Genetic Diagnostics in Adult-Onset Focal Segmental Glomerulosclerosis. Snoek R; Nguyen TQ; van der Zwaag B; van Zuilen AD; Kruis HME; van Gils-Verrij LA; Goldschmeding R; Knoers NVAM; Rookmaaker MB; van Eerde AM Nephron; 2019; 142(4):351-358. PubMed ID: 31096240 [TBL] [Abstract][Full Text] [Related]
13. Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis. Malone AF; Phelan PJ; Hall G; Cetincelik U; Homstad A; Alonso AS; Jiang R; Lindsey TB; Wu G; Sparks MA; Smith SR; Webb NJ; Kalra PA; Adeyemo AA; Shaw AS; Conlon PJ; Jennette JC; Howell DN; Winn MP; Gbadegesin RA Kidney Int; 2014 Dec; 86(6):1253-9. PubMed ID: 25229338 [TBL] [Abstract][Full Text] [Related]
14. Differentiating Primary, Genetic, and Secondary FSGS in Adults: A Clinicopathologic Approach. De Vriese AS; Sethi S; Nath KA; Glassock RJ; Fervenza FC J Am Soc Nephrol; 2018 Mar; 29(3):759-774. PubMed ID: 29321142 [TBL] [Abstract][Full Text] [Related]
15. Zhang P; Zhuo L; Zou Y; Li G; Peng K Clin Nephrol; 2019 Aug; 92(2):98-102. PubMed ID: 31198170 [No Abstract] [Full Text] [Related]