136 related articles for article (PubMed ID: 27719739)
1. 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]
2. 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]
3. WT1 and NPHS2 mutations in Korean children with steroid-resistant nephrotic syndrome.
Cho HY; Lee JH; Choi HJ; Lee BH; Ha IS; Choi Y; Cheong HI
Pediatr Nephrol; 2008 Jan; 23(1):63-70. PubMed ID: 17934764
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Mutations in WT1 in boys with sporadic isolated steroid-resistant nephrotic syndrome.
Yang Y; Zhao F; Tu X; Yu Z
Genet Mol Res; 2016 Mar; 15(1):15017559. PubMed ID: 26985958
[TBL] [Abstract][Full Text] [Related]
6. Wilms' tumor suppressor gene mutations in girls with sporadic isolated steroid-resistant nephrotic syndrome.
Yang YH; Zhao F; Feng DN; Wang JJ; Wang CF; Huang J; Nie XJ; Xia GZ; Chen GM; Yu ZH
Genet Mol Res; 2013 Dec; 12(4):6184-91. PubMed ID: 24338413
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms' tumor 1 (WT1) gene.
Megremis S; Mitsioni A; Fylaktou I; Tzeli SK; Komianou F; Stefanidis CJ; Kanavakis E; Traeger-Synodinos J
Eur J Pediatr; 2011 Dec; 170(12):1529-34. PubMed ID: 21499692
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Clinical characteristics and WT1 genetic analysis of patients with steroid resistant nephrotic syndrome accompanied with genitourinary malformations.
Li JG; Zhao D; Ding J; Xiao HJ; Guan N; Fan QF; Zhang HW
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Dec; 32(6):949-57. PubMed ID: 18182709
[TBL] [Abstract][Full Text] [Related]
12. [Clinical characteristics and WT1 genetic analysis of patients with steroid-resistant nephrotic syndrome accompanied with genitourinary malformations].
Li JG; Zhao D; Ding J; Xiao HJ; Fan QF; Guan N; Chen Y; Zhang HW
Zhonghua Er Ke Za Zhi; 2008 Sep; 46(9):692-7. PubMed ID: 19099861
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. WT1 gene mutations in Chinese children with early onset nephrotic syndrome.
Li J; Ding J; Zhao D; Yu Z; Fan Q; Chen Y; Zhang H; Zhong X; Huang J; Yao Y; Xiao H
Pediatr Res; 2010 Aug; 68(2):155-8. PubMed ID: 20442690
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A female infant with Frasier syndrome showing splice site mutation in Wilms' tumor gene (WT1) intron 9.
Fujita S; Sugimoto K; Miyazawa T; Yanagida H; Tabata N; Okada M; Takemura T
Clin Nephrol; 2010 Jun; 73(6):487-91. PubMed ID: 20497763
[TBL] [Abstract][Full Text] [Related]
18. Donor splice-site mutations in WT1 are responsible for Frasier syndrome.
Barbaux S; Niaudet P; Gubler MC; Grünfeld JP; Jaubert F; Kuttenn F; Fékété CN; Souleyreau-Therville N; Thibaud E; Fellous M; McElreavey K
Nat Genet; 1997 Dec; 17(4):467-70. PubMed ID: 9398852
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. WT1 deletion leading to severe 46,XY gonadal dysgenesis, Wilms tumor and gonadoblastoma: case report.
Finken MJ; Hendriks YM; van der Voorn JP; Veening MA; Lombardi MP; Rotteveel J
Horm Res Paediatr; 2015; 83(3):211-6. PubMed ID: 25613702
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
