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Journal Abstract Search

191 related items for PubMed ID: 21499692

  • 1. 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
    [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, APN Study Group.
    Kidney Int; 2004 Aug; 66(2):564-70. PubMed ID: 15253707
    [Abstract] [Full Text] [Related]

  • 3. 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 04; 12(4):6184-91. PubMed ID: 24338413
    [Abstract] [Full Text] [Related]

  • 4. 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 04; 426(1-2):177-181. PubMed ID: 27885584
    [Abstract] [Full Text] [Related]

  • 5. 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 04; 21(10):1393-8. PubMed ID: 16909243
    [Abstract] [Full Text] [Related]

  • 6. 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 11; 15(1):15017559. PubMed ID: 26985958
    [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 11; 144(2):276-280. PubMed ID: 27934809
    [Abstract] [Full Text] [Related]

  • 8. 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 11; 32(1):81-89. PubMed ID: 27300205
    [Abstract] [Full Text] [Related]

  • 9. 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, Members of the APN Study Group.
    Pediatr Res; 2006 Feb 11; 59(2):325-31. PubMed ID: 16439601
    [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, Guan N, Fan QF, Zhang HW.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Dec 11; 32(6):949-57. PubMed ID: 18182709
    [Abstract] [Full Text] [Related]

  • 11. Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.
    Wang F, Zhang Y, Mao J, Yu Z, Yi Z, Yu L, Sun J, Wei X, Ding F, Zhang H, Xiao H, Yao Y, Tan W, Lovric S, Ding J, Hildebrandt F.
    Pediatr Nephrol; 2017 Jul 11; 32(7):1181-1192. PubMed ID: 28204945
    [Abstract] [Full Text] [Related]

  • 12. 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 11; 63(11):104047. PubMed ID: 32891756
    [Abstract] [Full Text] [Related]

  • 13. 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 10; 18(1):3. PubMed ID: 28068926
    [Abstract] [Full Text] [Related]

  • 14. Isolated steroid-resistant nephrotic syndrome in a Chinese child carrying a de novo mutation in WT1 gene:a case report and literature review.
    Li Y, Tian C, Wang Y, Ma G, Chen R.
    BMC Pediatr; 2022 Jun 16; 22(1):349. PubMed ID: 35710404
    [Abstract] [Full Text] [Related]

  • 15. WT1-related disorders: more than Denys-Drash syndrome.
    Lopez-Gonzalez M, Ariceta G.
    Pediatr Nephrol; 2024 Sep 16; 39(9):2601-2609. PubMed ID: 38326647
    [Abstract] [Full Text] [Related]

  • 16. WT1 gene mutations in three girls with nephrotic syndrome.
    Ismaili K, Verdure V, Vandenhoute K, Janssen F, Hall M.
    Eur J Pediatr; 2008 May 16; 167(5):579-81. PubMed ID: 17541636
    [Abstract] [Full Text] [Related]

  • 17. Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
    Santín S, Bullich G, Tazón-Vega B, García-Maset R, Giménez I, Silva I, Ruíz P, Ballarín J, Torra R, Ars E.
    Clin J Am Soc Nephrol; 2011 May 16; 6(5):1139-48. PubMed ID: 21415313
    [Abstract] [Full Text] [Related]

  • 18. Early recognition of gonadal dysgenesis in congenital nephrotic syndrome
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    Ukarapong S, Berkovitz G, McElreavey K, Bashamboo A, Bao Y.
    Clin Nephrol; 2016 Dec 16; 86 (2016)(12):341-344. PubMed ID: 27719739
    [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, PodoNet Consortium.
    Kidney Int; 2014 May 16; 85(5):1169-78. PubMed ID: 24402088
    [Abstract] [Full Text] [Related]

  • 20. 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 16; 22(4):509-13. PubMed ID: 17216259
    [Abstract] [Full Text] [Related]

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