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Journal Abstract Search

174 related items for PubMed ID: 22763603

  • 1. A child with isolated nephrotic syndrome and WT1 mutation presenting as a 46, XY phenotypic male.
    Yang Y, Feng D, Huang J, Nie X, Yu Z.
    Eur J Pediatr; 2013 Jan; 172(1):127-9. PubMed ID: 22763603
    [Abstract] [Full Text] [Related]

  • 2. Different clinical presentations of WT1 gene mutations.
    Aydin M, Hakan N, Zenciroglu A, Aydog O, Okumus N.
    Eur J Pediatr; 2013 Dec; 172(12):1705-6. PubMed ID: 23835858
    [No 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; 21(10):1393-8. PubMed ID: 16909243
    [Abstract] [Full Text] [Related]

  • 4. Patients with different or identical genotypes of the WT1 gene present different phenotypes.
    Yang Y, Zhao F, Huang J, Nie X, Yu Z.
    Eur J Pediatr; 2013 Dec; 172(12):1707-8. PubMed ID: 23835859
    [No Abstract] [Full Text] [Related]

  • 5. 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]

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

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

  • 8. An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.
    Melo KF, Martin RM, Costa EM, Carvalho FM, Jorge AA, Arnhold IJ, Mendonca BB.
    J Clin Endocrinol Metab; 2002 Jun; 87(6):2500-5. PubMed ID: 12050205
    [Abstract] [Full Text] [Related]

  • 9. 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 Jun; 35(2):112-9. PubMed ID: 26882358
    [Abstract] [Full Text] [Related]

  • 10. Clinical Aspects of WT1 and the Kidney.
    Miller-Hodges E.
    Methods Mol Biol; 2016 Jun; 1467():15-21. PubMed ID: 27417956
    [Abstract] [Full Text] [Related]

  • 11. Denys-Drash syndrome with neonatal renal failure in monozygotic twins due to c.1097G>A mutation in the WT1 gene.
    Furtado LV, Pysher T, Opitz J, Lamb R, Comstock J, Batish S, Mauch T, Nelson R, Zhou H.
    Fetal Pediatr Pathol; 2011 Jun; 30(4):266-72. PubMed ID: 21434831
    [Abstract] [Full Text] [Related]

  • 12. 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; 38(1):124-9; discussion 124-9. PubMed ID: 12592634
    [Abstract] [Full Text] [Related]

  • 13. Detailed clinical manifestations at onset and prognosis of neonatal-onset Denys-Drash syndrome and congenital nephrotic syndrome of the Finnish type.
    Nishi K, Inoguchi T, Kamei K, Hamada R, Hataya H, Ogura M, Sato M, Yoshioka T, Ogata K, Ito S, Nakanishi K, Nozu K, Hamasaki Y, Ishikura K.
    Clin Exp Nephrol; 2019 Aug; 23(8):1058-1065. PubMed ID: 30963316
    [Abstract] [Full Text] [Related]

  • 14. Genetic forms of nephrotic syndrome: a single-center experience in Brussels.
    Ismaili K, Pawtowski A, Boyer O, Wissing KM, Janssen F, Hall M.
    Pediatr Nephrol; 2009 Feb; 24(2):287-94. PubMed ID: 18709391
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. [Clinical and pathological features and mutational types of WT1 mutation-associated nephropathy].
    Sun LZ, Wang HY, Li M, Lin HR, Wu JL, Tang W, Li YJ, Yue ZH, Liu T, Chen HM, Hu MY.
    Zhonghua Er Ke Za Zhi; 2018 Oct 02; 56(10):769-774. PubMed ID: 30293282
    [Abstract] [Full Text] [Related]

  • 17. 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 Oct 02; 11(3):361-7. PubMed ID: 22908070
    [Abstract] [Full Text] [Related]

  • 18. Nephrotic syndrome and end-stage renal disease with WT1 mutation detected at 3 years.
    Ito S, Ikeda M, Takata A, Kikuchi H, Hata J, Honda M.
    Pediatr Nephrol; 1999 Nov 02; 13(9):790-1. PubMed ID: 10603123
    [Abstract] [Full Text] [Related]

  • 19. [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 02; 26(156):642-4. PubMed ID: 19711733
    [Abstract] [Full Text] [Related]

  • 20. 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]

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