141 related articles for article (PubMed ID: 23295293)
21. 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]
22. [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]
23. 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]
24. 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]
25. Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.
Ruf RG; Schultheiss M; Lichtenberger A; Karle SM; Zalewski I; Mucha B; Everding AS; Neuhaus T; Patzer L; Plank C; Haas JP; Ozaltin F; Imm A; Fuchshuber A; Bakkaloglu A; Hildebrandt F;
Kidney Int; 2004 Aug; 66(2):564-70. PubMed ID: 15253707
[TBL] [Abstract][Full Text] [Related]
26. Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations.
Chernin G; Vega-Warner V; Schoeb DS; Heeringa SF; Ovunc B; Saisawat P; Cleper R; Ozaltin F; Hildebrandt F;
Clin J Am Soc Nephrol; 2010 Sep; 5(9):1655-62. PubMed ID: 20595692
[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. 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]
29. Early recognition of gonadal dysgenesis in congenital nephrotic syndrome
.
Ukarapong S; Berkovitz G; McElreavey K; Bashamboo A; Bao Y
Clin Nephrol; 2016 Dec; 86 (2016)(12):341-344. PubMed ID: 27719739
[TBL] [Abstract][Full Text] [Related]
30. Clinical and genetic findings of five patients with WT1-related disorders.
Andrade JG; Guaragna MS; Soardi FC; Guerra-Júnior G; Mello MP; Maciel-Guerra AT
Arq Bras Endocrinol Metabol; 2008 Nov; 52(8):1236-43. PubMed ID: 19169475
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases.
Denamur E; Bocquet N; Mougenot B; Da Silva F; Martinat L; Loirat C; Elion J; Bensman A; Ronco PM
J Am Soc Nephrol; 1999 Oct; 10(10):2219-23. PubMed ID: 10505700
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. 46,XY phenotypic male with focal segmental glomerulosclerosis caused by the WT1 splice site mutation.
Tajima T; Sasaki S; Tanaka Y; Kusunoki H; Nagashima T; Nonomura K; Fujieda K
Horm Res; 2003; 60(6):302-5. PubMed ID: 14646409
[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. Frasier syndrome: a cause of focal segmental glomerulosclerosis in a 46,XX female.
Demmer L; Primack W; Loik V; Brown R; Therville N; McElreavey K
J Am Soc Nephrol; 1999 Oct; 10(10):2215-8. PubMed ID: 10505699
[TBL] [Abstract][Full Text] [Related]
37. A Japanese case with Frasier syndrome caused by the splice junction mutation of WT1 gene.
Okuhara K; Tajima S; Nakae J; Sasaki S; Tochimaru H; Abe S; Fujieda K
Endocr J; 1999 Oct; 46(5):639-42. PubMed ID: 10670748
[TBL] [Abstract][Full Text] [Related]
38. WT1 and NPHS2 gene mutation analysis and clinical management of steroid-resistant nephrotic syndrome.
Ramanathan AS; Vijayan M; Rajagopal S; Rajendiran P; Senguttuvan P
Mol Cell Biochem; 2017 Feb; 426(1-2):177-181. PubMed ID: 27885584
[TBL] [Abstract][Full Text] [Related]
39. WT1 gene mutation responsible for male sex reversal and renal failure: the Frasier syndrome.
Saylam K; Simon P
Eur J Obstet Gynecol Reprod Biol; 2003 Sep; 110(1):111-3. PubMed ID: 12932885
[TBL] [Abstract][Full Text] [Related]
40. Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy.
Ahn YH; Park EJ; Kang HG; Kim SH; Cho HY; Shin JI; Lee JH; Park YS; Kim KS; Ha IS; Cheong HI
Pediatr Nephrol; 2017 Jan; 32(1):81-89. PubMed ID: 27300205
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]