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Journal Abstract Search

186 related items for PubMed ID: 38326647

  • 1. 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]

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

  • 3. 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; 63(11):104047. PubMed ID: 32891756
    [Abstract] [Full Text] [Related]

  • 4. 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]

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

  • 6. A novel WT1 gene mutation in a chinese girl with denys-drash syndrome.
    Wang F, Cai J, Wang J, He M, Mao J, Zhu K, Zhao M, Guan Z, Li L, Jin H, Shu Q.
    J Clin Lab Anal; 2021 May; 35(5):e23769. PubMed ID: 33942367
    [Abstract] [Full Text] [Related]

  • 7. Management of Wilms tumors in Drash and Frasier syndromes.
    Auber F, Jeanpierre C, Denamur E, Jaubert F, Schleiermacher G, Patte C, Cabrol S, Leverger G, Nihoul-Fékété C, Sarnacki S.
    Pediatr Blood Cancer; 2009 Jan; 52(1):55-9. PubMed ID: 18816692
    [Abstract] [Full Text] [Related]

  • 8. [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; 26(156):642-4. PubMed ID: 19711733
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. [Denys-Drash syndrome. Experience gathered in Erlangen illustrated by two case reports].
    Zugor V, Zenker M, Dötsch J, Schrott KM, Schott GE.
    Urologe A; 2005 Oct; 44(10):1197-200. PubMed ID: 16003530
    [Abstract] [Full Text] [Related]

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

  • 12. 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; 37(10):2369-2374. PubMed ID: 35211794
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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]

  • 15. WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease.
    Ferrari MTM, Watanabe A, da Silva TE, Gomes NL, Batista RL, Nishi MY, de Paula LCP, Costa EC, Costa EMF, Cukier P, Onuchic LF, Mendonca BB, Domenice S.
    Sex Dev; 2022 Aug; 16(1):46-54. PubMed ID: 34392242
    [Abstract] [Full Text] [Related]

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

  • 17. 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 Nov; 30(4):266-72. PubMed ID: 21434831
    [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; 40(2):113-120. PubMed ID: 31707902
    [Abstract] [Full Text] [Related]

  • 19. Bilateral Wilms' tumor in a child with Denys-Drash syndrome: novel frameshift variant disrupts the WT1 nuclear location signaling region.
    Guaragna MS, Ledesma FL, Manzano VZ, Maciel-Guerra AT, Guerra-Júnior G, Silva MM, Luiz de Brito P, Palandi de Mello M.
    J Pediatr Endocrinol Metab; 2022 Jun 27; 35(6):837-843. PubMed ID: 35304980
    [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 27; 295(1):F12-7. PubMed ID: 18385267
    [Abstract] [Full Text] [Related]

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