228 related articles for article (PubMed ID: 17061122)
21. [Glomerulopathy in Denys-Drash syndrome. Case report of a model disease].
Stallmach T; Neuhaus TJ; Kösters R; Hailemariam S
Pathologe; 1998 May; 19(3):230-4. PubMed ID: 9648150
[TBL] [Abstract][Full Text] [Related]
22. Sertoli cell tumor and gonadoblastoma in an untreated 29-year-old 46,XY phenotypic male with Frasier syndrome carrying a WT1 IVS9+4C>T mutation.
Kitsiou-Tzeli S; Deligiorgi M; Malaktari-Skarantavou S; Vlachopoulos C; Megremis S; Fylaktou I; Traeger-Synodinos J; Kanaka-Gantenbein C; Stefanadis C; Kanavakis E
Hormones (Athens); 2012; 11(3):361-7. PubMed ID: 22908070
[TBL] [Abstract][Full Text] [Related]
23. A familial WT1 mutation associated with incomplete Denys-Drash syndrome.
Zhu C; Zhao F; Zhang W; Wu H; Chen Y; Ding G; Zhang A; Huang S
Eur J Pediatr; 2013 Oct; 172(10):1357-62. PubMed ID: 23715653
[TBL] [Abstract][Full Text] [Related]
24. WT1 and glomerular diseases.
Niaudet P; Gubler MC
Pediatr Nephrol; 2006 Nov; 21(11):1653-60. PubMed ID: 16927106
[TBL] [Abstract][Full Text] [Related]
25. WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes.
Aucella F; Bisceglia L; De Bonis P; Gigante M; Caridi G; Barbano G; Mattioli G; Perfumo F; Gesualdo L; Ghiggeri GM
Pediatr Nephrol; 2006 Oct; 21(10):1393-8. PubMed ID: 16909243
[TBL] [Abstract][Full Text] [Related]
26. Frasier syndrome: four new cases with unusual presentations.
Guaragna MS; Lutaif AC; Bittencourt VB; Piveta CS; Soardi FC; Castro LC; Belangero VM; Maciel-Guerra AT; Guerra-Junior G; Mello MP
Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):525-32. PubMed ID: 23295293
[TBL] [Abstract][Full Text] [Related]
27. The Wt1+/R394W mouse displays glomerulosclerosis and early-onset renal failure characteristic of human Denys-Drash syndrome.
Gao F; Maiti S; Sun G; Ordonez NG; Udtha M; Deng JM; Behringer RR; Huff V
Mol Cell Biol; 2004 Nov; 24(22):9899-910. PubMed ID: 15509792
[TBL] [Abstract][Full Text] [Related]
28. Gonadal mosaicism of Frasier syndrome in 3 Chinese siblings with donor splice site mutation of Wilms' tumour gene.
Chak WL; To KF; Cheng YL; Tsui KM; Lo KL; Tong HM; Lai FM; Wong FK; Choi KS; Chau KF; Li CS
Nephron; 2002 Jul; 91(3):526-9. PubMed ID: 12119492
[TBL] [Abstract][Full Text] [Related]
29. [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]
30. 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]
31. 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]
32. WT1 Haploinsufficiency Supports Milder Renal Manifestation in Two Patients with Denys-Drash Syndrome.
Guaragna MS; Ribeiro de Andrade JG; de Freitas Carli B; Belangero VM; Maciel-Guerra AT; Guerra-Júnior G; de Mello MP
Sex Dev; 2017; 11(1):34-39. PubMed ID: 28081536
[TBL] [Abstract][Full Text] [Related]
33. WT1 mutation and podocyte molecular expression in a Chinese Frasier syndrome patient.
Li J; Zhao D; Ding J; Xiao H; Guan N; Fan Q; Zhang H
Pediatr Nephrol; 2007 Dec; 22(12):2133-6. PubMed ID: 17694336
[TBL] [Abstract][Full Text] [Related]
34. A child with isolated nephrotic syndrome and WT1 mutation presenting as a 46, XY phenotypic male.
Yang Y; Feng D; Huang J; Nie X; Yu Z
Eur J Pediatr; 2013 Jan; 172(1):127-9. PubMed ID: 22763603
[TBL] [Abstract][Full Text] [Related]
35. WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease.
Ferrari MTM; Watanabe A; da Silva TE; Gomes NL; Batista RL; Nishi MY; de Paula LCP; Costa EC; Costa EMF; Cukier P; Onuchic LF; Mendonca BB; Domenice S
Sex Dev; 2022; 16(1):46-54. PubMed ID: 34392242
[TBL] [Abstract][Full Text] [Related]
36. Expanding the clinical spectrum of Frasier syndrome.
Gwin K; Cajaiba MM; Caminoa-Lizarralde A; Picazo ML; Nistal M; Reyes-Múgica M
Pediatr Dev Pathol; 2008; 11(2):122-7. PubMed ID: 17378674
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Frasier syndrome: early gonadoblastoma and cyclosporine responsiveness.
Sinha A; Sharma S; Gulati A; Sharma A; Agarwala S; Hari P; Bagga A
Pediatr Nephrol; 2010 Oct; 25(10):2171-4. PubMed ID: 20419325
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Congenital diaphragmatic eventration with pulmonary dysplasia in Frasier syndrome due to a WT1 mutation of c.1432+5(IVS9)G>A.
Zhang B; Ding Y; Ren X; Song C; Zhang X; Wang F; Yang X
Eur J Med Genet; 2022 Dec; 65(12):104655. PubMed ID: 36341869
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
