176 related articles for article (PubMed ID: 20419325)
21. A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutation.
Hersmus R; van der Zwan YG; Stoop H; Bernard P; Sreenivasan R; Oosterhuis JW; Brüggenwirth HT; de Boer S; White S; Wolffenbuttel KP; Alders M; McElreavy K; Drop SL; Harley VR; Looijenga LH
PLoS One; 2012; 7(7):e40858. PubMed ID: 22815844
[TBL] [Abstract][Full Text] [Related]
22. Frasier syndrome: a rare cause of delayed puberty.
Chan WK; To KF; But WM; Lee KW
Hong Kong Med J; 2006 Jun; 12(3):225-7. PubMed ID: 16760553
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. [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]
26. [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]
27. Surgical management and genotype/phenotype correlations in WT1 gene-related diseases (Drash, Frasier syndromes).
Auber F; Lortat-Jacob S; Sarnacki S; Jaubert F; Salomon R; Thibaud E; Jeanpierre C; Nihoul-Fékété C
J Pediatr Surg; 2003 Jan; 38(1):124-9; discussion 124-9. PubMed ID: 12592634
[TBL] [Abstract][Full Text] [Related]
28. Gonadal tumor in Frasier syndrome: a review and classification.
Ezaki J; Hashimoto K; Asano T; Kanda S; Akioka Y; Hattori M; Yamamoto T; Shibata N
Cancer Prev Res (Phila); 2015 Apr; 8(4):271-6. PubMed ID: 25623218
[TBL] [Abstract][Full Text] [Related]
29. WT1 gene mutations in three girls with nephrotic syndrome.
Ismaili K; Verdure V; Vandenhoute K; Janssen F; Hall M
Eur J Pediatr; 2008 May; 167(5):579-81. PubMed ID: 17541636
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Wilms' tumour 1 gene mutations in south Indian children with steroid-resistant nephrotic syndrome.
Kumar AS; Srilakshmi R; Karthickeyan S; Balakrishnan K; Padmaraj R; Senguttuvan P
Indian J Med Res; 2016 Aug; 144(2):276-280. PubMed ID: 27934809
[TBL] [Abstract][Full Text] [Related]
32. Genotype-phenotype associations in WT1 glomerulopathy.
Lipska BS; Ranchin B; Iatropoulos P; Gellermann J; Melk A; Ozaltin F; Caridi G; Seeman T; Tory K; Jankauskiene A; Zurowska A; Szczepanska M; Wasilewska A; Harambat J; Trautmann A; Peco-Antic A; Borzecka H; Moczulska A; Saeed B; Bogdanovic R; Kalyoncu M; Simkova E; Erdogan O; Vrljicak K; Teixeira A; Azocar M; Schaefer F;
Kidney Int; 2014 May; 85(5):1169-78. PubMed ID: 24402088
[TBL] [Abstract][Full Text] [Related]
33. Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population.
Orloff MS; Iyengar SK; Winkler CA; Goddard KA; Dart RA; Ahuja TS; Mokrzycki M; Briggs WA; Korbet SM; Kimmel PL; Simon EE; Trachtman H; Vlahov D; Michel DM; Berns JS; Smith MC; Schelling JR; Sedor JR; Kopp JB
Physiol Genomics; 2005 Apr; 21(2):212-21. PubMed ID: 15687485
[TBL] [Abstract][Full Text] [Related]
34. Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations.
Gellermann J; Stefanidis CJ; Mitsioni A; Querfeld U
Pediatr Nephrol; 2010 Jul; 25(7):1285-9. PubMed ID: 20191369
[TBL] [Abstract][Full Text] [Related]
35. Frasier Syndrome: A Rare Cause of Refractory Steroid-Resistant Nephrotic Syndrome.
Huang YC; Tsai MC; Tsai CR; Fu LS
Children (Basel); 2021 Jul; 8(8):. PubMed ID: 34438508
[TBL] [Abstract][Full Text] [Related]
36. Lack of puberty despite elevated estradiol in a 46,XY phenotypic female with Frasier syndrome.
Miyoshi Y; Santo Y; Tachikawa K; Namba N; Hirai H; Mushiake S; Nakajima S; Michigami T; Ozono K
Endocr J; 2006 Jun; 53(3):371-6. PubMed ID: 16717397
[TBL] [Abstract][Full Text] [Related]
37. Frasier Syndrome: A 15-Year-Old Phenotypically Female Adolescent Presenting with Delayed Puberty and Nephropathy.
Shao Q; Xie X; Geng J; Yang X; Li W; Zhang Y
Children (Basel); 2023 Mar; 10(3):. PubMed ID: 36980135
[TBL] [Abstract][Full Text] [Related]
38. Frasier syndrome, a potential cause of end-stage renal failure in childhood.
Bache M; Dheu C; Doray B; Fothergill H; Soskin S; Paris F; Sultan C; Fischbach M
Pediatr Nephrol; 2010 Mar; 25(3):549-52. PubMed ID: 19921279
[TBL] [Abstract][Full Text] [Related]
39. A Unique Presentation of XY Gonadal Dysgenesis in Frasier Syndrome due to WT1 Mutation and a Literature Review.
Lavi E; Zighan M; Abu Libdeh A; Klopstock T; Weinberg-Shukron A; Renbaum P; Levy-Lahad E; Zangen D
Pediatr Endocrinol Rev; 2020 Aug; 17(4):302-307. PubMed ID: 32780953
[TBL] [Abstract][Full Text] [Related]
40. Focal segmental glomerulosclerosis: pathogenesis and treatment.
Benchimol C
Curr Opin Pediatr; 2003 Apr; 15(2):171-80. PubMed ID: 12640274
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]