348 related articles for article (PubMed ID: 16909243)
1. 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]
2. 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]
3. 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]
4. 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]
5. Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome.
Gbadegesin R; Hinkes B; Vlangos C; Mucha B; Liu J; Hopcian J; Hildebrandt F
Pediatr Nephrol; 2007 Apr; 22(4):509-13. PubMed ID: 17216259
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. WT1 and glomerular diseases.
Niaudet P; Gubler MC
Pediatr Nephrol; 2006 Nov; 21(11):1653-60. PubMed ID: 16927106
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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]
16. Gonad development in Drash and Frasier syndromes depends on WT1 mutations.
Jaubert F; Vasiliu V; Patey-Mariaud de Serre N; Auber F; Jeanpierre C; Gubler MC; Nihoul-Fékété C; Fellous M
Arkh Patol; 2003; 65(2):40-4. PubMed ID: 15357247
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Different clinical presentations of WT1 gene mutations.
Aydin M; Hakan N; Zenciroglu A; Aydog O; Okumus N
Eur J Pediatr; 2013 Dec; 172(12):1705-6. PubMed ID: 23835858
[No Abstract] [Full Text] [Related]
19. Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome.
Büscher AK; Beck BB; Melk A; Hoefele J; Kranz B; Bamborschke D; Baig S; Lange-Sperandio B; Jungraithmayr T; Weber LT; Kemper MJ; Tönshoff B; Hoyer PF; Konrad M; Weber S;
Clin J Am Soc Nephrol; 2016 Feb; 11(2):245-53. PubMed ID: 26668027
[TBL] [Abstract][Full Text] [Related]
20. Genetic forms of nephrotic syndrome: a single-center experience in Brussels.
Ismaili K; Pawtowski A; Boyer O; Wissing KM; Janssen F; Hall M
Pediatr Nephrol; 2009 Feb; 24(2):287-94. PubMed ID: 18709391
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
