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140 related items for PubMed ID: 17694336

  • 1. WT1 mutation and podocyte molecular expression in a Chinese Frasier syndrome patient.
    Li J, Zhao D, Ding J, Xiao H, Guan N, Fan Q, Zhang H.
    Pediatr Nephrol; 2007 Dec; 22(12):2133-6. PubMed ID: 17694336
    [Abstract] [Full Text] [Related]

  • 2. [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
    [Abstract] [Full Text] [Related]

  • 3. A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis.
    Benetti E, Caridi G, Malaventura C, Dagnino M, Leonardi E, Artifoni L, Ghiggeri GM, Tosatto SC, Murer L.
    Clin J Am Soc Nephrol; 2010 Apr; 5(4):698-702. PubMed ID: 20150449
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases.
    Denamur E, Bocquet N, Mougenot B, Da Silva F, Martinat L, Loirat C, Elion J, Bensman A, Ronco PM.
    J Am Soc Nephrol; 1999 Oct; 10(10):2219-23. PubMed ID: 10505700
    [Abstract] [Full Text] [Related]

  • 6. WT1 intron 9 splice acceptor site mutation in a 46,XY male with focal segmental glomerulosclerosis.
    Kanemoto K, Ishikura K, Ariyasu D, Hamasaki Y, Hataya H, Hasegawa Y, Ikeda M.
    Pediatr Nephrol; 2007 Mar; 22(3):454-8. PubMed ID: 17061122
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. [Frasier syndrome: a rare syndrome with WT1 gene mutation in pediatric urology].
    Zugor V, Zenker M, Schrott KM, Schott GE.
    Aktuelle Urol; 2006 Jan; 37(1):64-6. PubMed ID: 16440249
    [Abstract] [Full Text] [Related]

  • 9. WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis.
    Denamur E, Bocquet N, Baudouin V, Da Silva F, Veitia R, Peuchmaur M, Elion J, Gubler MC, Fellous M, Niaudet P, Loirat C.
    Kidney Int; 2000 May; 57(5):1868-72. PubMed ID: 10792605
    [Abstract] [Full Text] [Related]

  • 10. Frasier syndrome: a cause of focal segmental glomerulosclerosis in a 46,XX female.
    Demmer L, Primack W, Loik V, Brown R, Therville N, McElreavey K.
    J Am Soc Nephrol; 1999 Oct; 10(10):2215-8. PubMed ID: 10505699
    [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; 25(10):2171-4. PubMed ID: 20419325
    [Abstract] [Full Text] [Related]

  • 12. 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; 5(9):1655-62. PubMed ID: 20595692
    [Abstract] [Full Text] [Related]

  • 13. Characteristics of testicular dysgenesis syndrome and decreased expression of SRY and SOX9 in Frasier syndrome.
    Schumacher V, Gueler B, Looijenga LH, Becker JU, Amann K, Engers R, Dotsch J, Stoop H, Schulz W, Royer-Pokora B.
    Mol Reprod Dev; 2008 Sep; 75(9):1484-94. PubMed ID: 18271004
    [Abstract] [Full Text] [Related]

  • 14. Frasier syndrome, a potential cause of end-stage renal failure in childhood.
    Bache M, Dheu C, Doray B, Fothergill H, Soskin S, Paris F, Sultan C, Fischbach M.
    Pediatr Nephrol; 2010 Mar; 25(3):549-52. PubMed ID: 19921279
    [Abstract] [Full Text] [Related]

  • 15. Expanding the clinical spectrum of Frasier syndrome.
    Gwin K, Cajaiba MM, Caminoa-Lizarralde A, Picazo ML, Nistal M, Reyes-Múgica M.
    Pediatr Dev Pathol; 2008 Mar; 11(2):122-7. PubMed ID: 17378674
    [Abstract] [Full Text] [Related]

  • 16. Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population.
    Orloff MS, Iyengar SK, Winkler CA, Goddard KA, Dart RA, Ahuja TS, Mokrzycki M, Briggs WA, Korbet SM, Kimmel PL, Simon EE, Trachtman H, Vlahov D, Michel DM, Berns JS, Smith MC, Schelling JR, Sedor JR, Kopp JB.
    Physiol Genomics; 2005 Apr 14; 21(2):212-21. PubMed ID: 15687485
    [Abstract] [Full Text] [Related]

  • 17. WT1 and glomerular diseases.
    Niaudet P, Gubler MC.
    Pediatr Nephrol; 2006 Nov 14; 21(11):1653-60. PubMed ID: 16927106
    [Abstract] [Full Text] [Related]

  • 18. 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 14; 426(1-2):177-181. PubMed ID: 27885584
    [Abstract] [Full Text] [Related]

  • 19. 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 14; 295(1):F12-7. PubMed ID: 18385267
    [Abstract] [Full Text] [Related]

  • 20. 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 14; 17(4):467-70. PubMed ID: 9398852
    [Abstract] [Full Text] [Related]

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