532 related articles for article (PubMed ID: 15253707)
1. 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]
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. Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.
Mucha B; Ozaltin F; Hinkes BG; Hasselbacher K; Ruf RG; Schultheiss M; Hangan D; Hoskins BE; Everding AS; Bogdanovic R; Seeman T; Hoppe B; Hildebrandt F;
Pediatr Res; 2006 Feb; 59(2):325-31. PubMed ID: 16439601
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
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. [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]
11. 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]
12. 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]
13. 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]
14. Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.
Ruf RG; Lichtenberger A; Karle SM; Haas JP; Anacleto FE; Schultheiss M; Zalewski I; Imm A; Ruf EM; Mucha B; Bagga A; Neuhaus T; Fuchshuber A; Bakkaloglu A; Hildebrandt F;
J Am Soc Nephrol; 2004 Mar; 15(3):722-32. PubMed ID: 14978175
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohort.
Sun S; Xu L; Bi Y; Wang J; Zhang Z; Tang X; Cao Q; Zhai Y; Chen J; Fang X; Liu J; Fang Y; Xiang T; Qian Y; Wu B; Wang H; Zhou W; Shen J; Dong K; Liu X; Zheng B; Zhang A; Wang X; Wu Y; Ma D; Shen Q; Rao J; Xu H
Eur J Med Genet; 2020 Nov; 63(11):104047. PubMed ID: 32891756
[TBL] [Abstract][Full Text] [Related]
17. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).
Hinkes BG; Mucha B; Vlangos CN; Gbadegesin R; Liu J; Hasselbacher K; Hangan D; Ozaltin F; Zenker M; Hildebrandt F;
Pediatrics; 2007 Apr; 119(4):e907-19. PubMed ID: 17371932
[TBL] [Abstract][Full Text] [Related]
18. Screening of WT1 mutations in exon 8 and 9 in children with steroid resistant nephrotic syndrome from a single centre and establishment of a rapid screening assay using high-resolution melting analysis in a clinical setting.
Siji A; Pardeshi VC; Ravindran S; Vasudevan A; Vasudevan A
BMC Med Genet; 2017 Jan; 18(1):3. PubMed ID: 28068926
[TBL] [Abstract][Full Text] [Related]
19. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
Weber S; Gribouval O; Esquivel EL; Morinière V; Tête MJ; Legendre C; Niaudet P; Antignac C
Kidney Int; 2004 Aug; 66(2):571-9. PubMed ID: 15253708
[TBL] [Abstract][Full Text] [Related]
20. TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome.
Mir S; Yavascan O; Berdeli A; Sozeri B
Nephrol Dial Transplant; 2012 Jan; 27(1):205-9. PubMed ID: 21511817
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
