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Journal Abstract Search

187 related items for PubMed ID: 32838737

  • 1. Immune-complex glomerulonephritis with a membranoproliferative pattern in Frasier syndrome: a case report and review of the literature.
    Matsuoka D, Noda S, Kamiya M, Hidaka Y, Shimojo H, Yamada Y, Miyamoto T, Nozu K, Iijima K, Tsukaguchi H.
    BMC Nephrol; 2020 Aug 24; 21(1):362. PubMed ID: 32838737
    [Abstract] [Full Text] [Related]

  • 2. WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review.
    Anderson E, Aldridge M, Turner R, Harraway J, McManus S, Stewart A, Borzi P, Trnka P, Burke J, Coman D.
    Pediatr Nephrol; 2022 Oct 24; 37(10):2369-2374. PubMed ID: 35211794
    [Abstract] [Full Text] [Related]

  • 3. 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 24; 10(10):2215-8. PubMed ID: 10505699
    [Abstract] [Full Text] [Related]

  • 4. 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 24; 22(3):454-8. PubMed ID: 17061122
    [Abstract] [Full Text] [Related]

  • 5. 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 24; 11(2):122-7. PubMed ID: 17378674
    [Abstract] [Full Text] [Related]

  • 6. 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 24; 5(4):698-702. PubMed ID: 20150449
    [Abstract] [Full Text] [Related]

  • 7. [Frasier syndrome: a rare syndrome with WT1 gene mutation in pediatric urology].
    Zugor V, Zenker M, Schrott KM, Schott GE.
    Aktuelle Urol; 2006 Jan 24; 37(1):64-6. PubMed ID: 16440249
    [Abstract] [Full Text] [Related]

  • 8. 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 24; 25(10):2171-4. PubMed ID: 20419325
    [Abstract] [Full Text] [Related]

  • 9. Dense intramembranous deposit disease: new pathologic features.
    Sibley RK, Kim Y.
    Kidney Int; 1984 Apr 24; 25(4):660-70. PubMed ID: 6482170
    [Abstract] [Full Text] [Related]

  • 10. 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 24; 57(5):1868-72. PubMed ID: 10792605
    [Abstract] [Full Text] [Related]

  • 11. 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 24; 73(6):487-91. PubMed ID: 20497763
    [Abstract] [Full Text] [Related]

  • 12. Wilms' tumor and glomerular disease. Occurrence with features of membranoproliferative glomerulonephritis and secondary focal, segmental glomerulosclerosis.
    Thorner P, McGraw M, Weitzman S, Balfe JW, Klein M, Baumal R.
    Arch Pathol Lab Med; 1984 Feb 24; 108(2):141-6. PubMed ID: 6320757
    [Abstract] [Full Text] [Related]

  • 13. 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 Feb 24; 11(3):361-7. PubMed ID: 22908070
    [Abstract] [Full Text] [Related]

  • 14. 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 24; 10(10):2219-23. PubMed ID: 10505700
    [Abstract] [Full Text] [Related]

  • 15. A patient with focal segmental glomerulosclerosis and acute renal failure due to crescentic membranoproliferative glomerulonephritis.
    Chan PC, Chan KW, Cheng IK.
    Nephron; 1991 Oct 24; 57(2):232-5. PubMed ID: 2020354
    [Abstract] [Full Text] [Related]

  • 16. 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 24; 21(10):1393-8. PubMed ID: 16909243
    [Abstract] [Full Text] [Related]

  • 17. 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 24; 85(5):1169-78. PubMed ID: 24402088
    [Abstract] [Full Text] [Related]

  • 18. Focal Segmental Membranoproliferative Glomerulonephritis: A Histological Variant of Denys-Drash Syndrome.
    Karmila AB, Yap YC, Appadurai M, Oh L, Fazarina M, Abd Ghani F, Ariffin H.
    Fetal Pediatr Pathol; 2021 Apr 24; 40(2):113-120. PubMed ID: 31707902
    [Abstract] [Full Text] [Related]

  • 19. Pattern of glomerulonephritis in Singapore children--a renal biopsy perspective.
    Yap HK, Murugasu B, Saw AH, Chiang GS, Tay JS, Wong HB, Tan CL, Lim CH.
    Ann Acad Med Singap; 1989 Jan 24; 18(1):35-9. PubMed ID: 2712516
    [Abstract] [Full Text] [Related]

  • 20. Acute glomerulonephritis superimposed on focal segmental glomerulosclerosis: a case report.
    Tanaka H, Waga S, Nakahata T, Kondo N, Onodera N, Monma N.
    Tohoku J Exp Med; 2000 Jul 24; 191(3):177-81. PubMed ID: 10997558
    [Abstract] [Full Text] [Related]

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