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.
176 related articles for article (PubMed ID: 35211794)
1. WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review. Anderson E; Aldridge M; Turner R; Harraway J; McManus S; Stewart A; Borzi P; Trnka P; Burke J; Coman D Pediatr Nephrol; 2022 Oct; 37(10):2369-2374. PubMed ID: 35211794 [TBL] [Abstract][Full Text] [Related]
2. Focal Segmental Membranoproliferative Glomerulonephritis: A Histological Variant of Denys-Drash Syndrome. Karmila AB; Yap YC; Appadurai M; Oh L; Fazarina M; Abd Ghani F; Ariffin H Fetal Pediatr Pathol; 2021 Apr; 40(2):113-120. PubMed ID: 31707902 [No Abstract] [Full Text] [Related]
3. Immune-complex glomerulonephritis with a membranoproliferative pattern in Frasier syndrome: a case report and review of the literature. Matsuoka D; Noda S; Kamiya M; Hidaka Y; Shimojo H; Yamada Y; Miyamoto T; Nozu K; Iijima K; Tsukaguchi H BMC Nephrol; 2020 Aug; 21(1):362. PubMed ID: 32838737 [TBL] [Abstract][Full Text] [Related]
4. Recurrence of membranoproliferative glomerulonephritis after renal transplantation in Denys-Drash. Neuhaus TJ; Arnold W; Gaspert A; Hopfer H; Fischer A Pediatr Nephrol; 2011 Feb; 26(2):317-22. PubMed ID: 21046168 [TBL] [Abstract][Full Text] [Related]
5. [WT1 mutation as a cause of progressive nephropathy in Frasier syndrome--case report]. Wasilewska A; Zoch-Zwierz W; Tenderenda E; Rybi-Szumińska A; Kołodziejczyk Z Pol Merkur Lekarski; 2009 Jun; 26(156):642-4. PubMed ID: 19711733 [TBL] [Abstract][Full Text] [Related]
7. WT1 intron 9 splice acceptor site mutation in a 46,XY male with focal segmental glomerulosclerosis. Kanemoto K; Ishikura K; Ariyasu D; Hamasaki Y; Hataya H; Hasegawa Y; Ikeda M Pediatr Nephrol; 2007 Mar; 22(3):454-8. PubMed ID: 17061122 [TBL] [Abstract][Full Text] [Related]
8. An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis. Melo KF; Martin RM; Costa EM; Carvalho FM; Jorge AA; Arnhold IJ; Mendonca BB J Clin Endocrinol Metab; 2002 Jun; 87(6):2500-5. PubMed ID: 12050205 [TBL] [Abstract][Full Text] [Related]
9. WT1-related disorders: more than Denys-Drash syndrome. Lopez-Gonzalez M; Ariceta G Pediatr Nephrol; 2024 Sep; 39(9):2601-2609. PubMed ID: 38326647 [TBL] [Abstract][Full Text] [Related]
10. [Frasier syndrome: a rare syndrome with WT1 gene mutation in pediatric urology]. Zugor V; Zenker M; Schrott KM; Schott GE Aktuelle Urol; 2006 Jan; 37(1):64-6. PubMed ID: 16440249 [TBL] [Abstract][Full Text] [Related]
11. Molecular analysis of Frasier syndrome: mutation in the WT1 gene in a girl with gonadal dysgenesis and nephronophthisis. Pérez de Nanclares G; Castaño L; Bilbao JR; Vallo A; Rica I; Vela A; Martul P J Pediatr Endocrinol Metab; 2002; 15(7):1047-50. PubMed ID: 12199335 [TBL] [Abstract][Full Text] [Related]
12. Bilateral Wilms' tumor in a child with Denys-Drash syndrome: novel frameshift variant disrupts the WT1 nuclear location signaling region. Guaragna MS; Ledesma FL; Manzano VZ; Maciel-Guerra AT; Guerra-Júnior G; Silva MM; Luiz de Brito P; Palandi de Mello M J Pediatr Endocrinol Metab; 2022 Jun; 35(6):837-843. PubMed ID: 35304980 [TBL] [Abstract][Full Text] [Related]
13. Clinical Aspects of WT1 and the Kidney. Miller-Hodges E Methods Mol Biol; 2016; 1467():15-21. PubMed ID: 27417956 [TBL] [Abstract][Full Text] [Related]
14. Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms. Klamt B; Koziell A; Poulat F; Wieacker P; Scambler P; Berta P; Gessler M Hum Mol Genet; 1998 Apr; 7(4):709-14. PubMed ID: 9499425 [TBL] [Abstract][Full Text] [Related]
15. Nephropathy with Wilms tumour or gonadal dysgenesis: incomplete Denys-Drash syndrome or separate diseases? Schmitt K; Zabel B; Tulzer G; Eitelberger F; Pelletier J Eur J Pediatr; 1995 Jul; 154(7):577-81. PubMed ID: 7556327 [TBL] [Abstract][Full Text] [Related]
17. A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys-Drash syndrome. da Silva TE; Nishi MY; Costa EM; Martin RM; Carvalho FM; Mendonca BB; Domenice S Pediatr Nephrol; 2011 Aug; 26(8):1311-5. PubMed ID: 21559934 [TBL] [Abstract][Full Text] [Related]