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4. 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]
5. [Clinical and pathological features of Denys-Drash syndrome: report of 3 cases]. Wang HY; Sun LZ; Yue ZH; Yang J; Jiang XY; Mo Y Zhonghua Er Ke Za Zhi; 2012 Nov; 50(11):855-8. PubMed ID: 23302619 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. A novel WT1 gene mutation in a newborn infant diagnosed with Denys-Drash syndrome. Hakan N; Aydin M; Erdogan O; Cavusoglu YH; Aycan Z; Ozaltin F; Zenciroglu A; Apaydin S; Gunes R; Sahin G; Cinar G; Okumus N Genet Couns; 2012; 23(2):255-61. PubMed ID: 22876585 [TBL] [Abstract][Full Text] [Related]
8. A novel WT1 gene mutation in a chinese girl with denys-drash syndrome. Wang F; Cai J; Wang J; He M; Mao J; Zhu K; Zhao M; Guan Z; Li L; Jin H; Shu Q J Clin Lab Anal; 2021 May; 35(5):e23769. PubMed ID: 33942367 [TBL] [Abstract][Full Text] [Related]
10. Hemolytic uremic syndrome as the presenting manifestation of WT1 mutation and Denys-Drash syndrome: a case report. Alge JL; Wenderfer SE; Hicks J; Bekheirnia MR; Schady DA; Kain JS; Braun MC BMC Nephrol; 2017 Jul; 18(1):243. PubMed ID: 28720077 [TBL] [Abstract][Full Text] [Related]
11. Effects of Denys-Drash syndrome point mutations on the DNA binding activity of the Wilms' tumor suppressor protein WT1. Borel F; Barilla KC; Hamilton TB; Iskandar M; Romaniuk PJ Biochemistry; 1996 Sep; 35(37):12070-6. PubMed ID: 8810912 [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 pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children. Yue Z; Pei Y; Sun L; Huang W; Huang H; Hu B; Yang J; Jiang X; Mo Y; Chen S; Lai KN; Wang Y Ren Fail; 2011; 33(9):910-4. PubMed ID: 21851196 [TBL] [Abstract][Full Text] [Related]
14. Denys-Drash syndrome with neonatal renal failure in monozygotic twins due to c.1097G>A mutation in the WT1 gene. Furtado LV; Pysher T; Opitz J; Lamb R; Comstock J; Batish S; Mauch T; Nelson R; Zhou H Fetal Pediatr Pathol; 2011; 30(4):266-72. PubMed ID: 21434831 [TBL] [Abstract][Full Text] [Related]
15. Prophylactic bilateral nephrectomy and preemptive kidney transplantation for Denys-Drash syndrome prior to development of kidney failure. Hosokawa C; Hotta K; Okamoto T; Cho Y; Hirose T; Iwahara N; Manabe A; Shinohara N Pediatr Nephrol; 2024 Mar; 39(3):905-909. PubMed ID: 37572117 [TBL] [Abstract][Full Text] [Related]
16. A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X. Heathcott RW; Morison IM; Gubler MC; Corbett R; Reeve AE Hum Mutat; 2002 Apr; 19(4):462. PubMed ID: 11933209 [TBL] [Abstract][Full Text] [Related]
17. Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations. Schumacher V; Schärer K; Wühl E; Altrogge H; Bonzel KE; Guschmann M; Neuhaus TJ; Pollastro RM; Kuwertz-Bröking E; Bulla M; Tondera AM; Mundel P; Helmchen U; Waldherr R; Weirich A; Royer-Pokora B Kidney Int; 1998 Jun; 53(6):1594-600. PubMed ID: 9607189 [TBL] [Abstract][Full Text] [Related]
18. [Clinical and pathological features and mutational types of WT1 mutation-associated nephropathy]. Sun LZ; Wang HY; Li M; Lin HR; Wu JL; Tang W; Li YJ; Yue ZH; Liu T; Chen HM; Hu MY Zhonghua Er Ke Za Zhi; 2018 Oct; 56(10):769-774. PubMed ID: 30293282 [No Abstract] [Full Text] [Related]
19. Novel WT1 mutation (C388Y) in a female child with Denys-Drash syndrome. Swiatecka-Urban A; Mokrzycki MH; Kaskel F; Da Silva F; Denamur E Pediatr Nephrol; 2001 Aug; 16(8):627-30. PubMed ID: 11519891 [TBL] [Abstract][Full Text] [Related]