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170 related items for PubMed ID: 17541636

  • 1. WT1 gene mutations in three girls with nephrotic syndrome.
    Ismaili K, Verdure V, Vandenhoute K, Janssen F, Hall M.
    Eur J Pediatr; 2008 May; 167(5):579-81. PubMed ID: 17541636
    [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 04; 12(4):6184-91. PubMed ID: 24338413
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. 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 11; 85(5):1169-78. PubMed ID: 24402088
    [Abstract] [Full Text] [Related]

  • 6. Refining the Diagnosis of Congenital Nephrotic Syndrome on Long-term Stored Tissue: c.1097G>A (p.(Arg366His)) WT1 Mutation Causing Denys Drash Syndrome.
    Hillen LM, Kamsteeg EJ, Schoots J, Tiebosch AT, Speel EJ, Roemen GM, Peutz-Koostra CJ, Stumpel CT.
    Fetal Pediatr Pathol; 2016 May 11; 35(2):112-9. PubMed ID: 26882358
    [Abstract] [Full Text] [Related]

  • 7. 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, Members of the GPN Study Group.
    Clin J Am Soc Nephrol; 2010 Sep 11; 5(9):1655-62. PubMed ID: 20595692
    [Abstract] [Full Text] [Related]

  • 8. 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 11; 170(12):1529-34. PubMed ID: 21499692
    [Abstract] [Full Text] [Related]

  • 9. 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 11; 38(1):124-9; discussion 124-9. PubMed ID: 12592634
    [Abstract] [Full Text] [Related]

  • 10. [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 11; 26(156):642-4. PubMed ID: 19711733
    [Abstract] [Full Text] [Related]

  • 11. Frasier syndrome: early gonadoblastoma and cyclosporine responsiveness.
    Sinha A, Sharma S, Gulati A, Sharma A, Agarwala S, Hari P, Bagga A.
    Pediatr Nephrol; 2010 Oct 11; 25(10):2171-4. PubMed ID: 20419325
    [Abstract] [Full Text] [Related]

  • 12. WT1 and glomerular diseases.
    Niaudet P, Gubler MC.
    Pediatr Nephrol; 2006 Nov 11; 21(11):1653-60. PubMed ID: 16927106
    [Abstract] [Full Text] [Related]

  • 13. Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?
    Koziell A, Charmandari E, Hindmarsh PC, Rees L, Scambler P, Brook CG.
    Clin Endocrinol (Oxf); 2000 Apr 11; 52(4):519-24. PubMed ID: 10762296
    [Abstract] [Full Text] [Related]

  • 14. WT1 mutations in steroid-resistant idiopathic nephrotic syndrome.
    Mishra OP, Singh AK, Abhinay A, Narayan G, Prasad R, Batra VV.
    Saudi J Kidney Dis Transpl; 2016 Mar 11; 27(2):417-8. PubMed ID: 26997404
    [No Abstract] [Full Text] [Related]

  • 15. WT1-related disorders: more than Denys-Drash syndrome.
    Lopez-Gonzalez M, Ariceta G.
    Pediatr Nephrol; 2024 Sep 11; 39(9):2601-2609. PubMed ID: 38326647
    [Abstract] [Full Text] [Related]

  • 16. The podocyte as a target: cyclosporin A in the management of the nephrotic syndrome caused by WT1 mutations.
    Stefanidis CJ, Querfeld U.
    Eur J Pediatr; 2011 Nov 11; 170(11):1377-83. PubMed ID: 21298518
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. 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, Arbeitsgemeinschaft für Paediatrische Nephrologie Study Group.
    Pediatrics; 2007 Apr 11; 119(4):e907-19. PubMed ID: 17371932
    [Abstract] [Full Text] [Related]

  • 19. Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations.
    Schumacher V, Schärer K, Wühl E, Altrogge H, Bonzel KE, Guschmann M, Neuhaus TJ, Pollastro RM, Kuwertz-Bröking E, Bulla M, Tondera AM, Mundel P, Helmchen U, Waldherr R, Weirich A, Royer-Pokora B.
    Kidney Int; 1998 Jun 11; 53(6):1594-600. PubMed ID: 9607189
    [Abstract] [Full Text] [Related]

  • 20. New insights into the function of the Wilms tumor suppressor gene WT1 in podocytes.
    Morrison AA, Viney RL, Saleem MA, Ladomery MR.
    Am J Physiol Renal Physiol; 2008 Jul 11; 295(1):F12-7. PubMed ID: 18385267
    [Abstract] [Full Text] [Related]

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