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Journal Abstract Search

161 related items for PubMed ID: 10603123

  • 21. 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; 85(5):1169-78. PubMed ID: 24402088
    [Abstract] [Full Text] [Related]

  • 22. [Glomerulopathy in Denys-Drash syndrome. Case report of a model disease].
    Stallmach T, Neuhaus TJ, Kösters R, Hailemariam S.
    Pathologe; 1998 May; 19(3):230-4. PubMed ID: 9648150
    [Abstract] [Full Text] [Related]

  • 23. 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]

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

  • 25. Software and database for the analysis of mutations in the human WT1 gene.
    Jeanpierre C, Béroud C, Niaudet P, Junien C.
    Nucleic Acids Res; 1998 Jan 01; 26(1):271-4. PubMed ID: 9399851
    [Abstract] [Full Text] [Related]

  • 26. A zinc finger truncation of murine WT1 results in the characteristic urogenital abnormalities of Denys-Drash syndrome.
    Patek CE, Little MH, Fleming S, Miles C, Charlieu JP, Clarke AR, Miyagawa K, Christie S, Doig J, Harrison DJ, Porteous DJ, Brookes AJ, Hooper ML, Hastie ND.
    Proc Natl Acad Sci U S A; 1999 Mar 16; 96(6):2931-6. PubMed ID: 10077614
    [Abstract] [Full Text] [Related]

  • 27.
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  • 28. Atypical presentation of Denys-Drash syndrome in a female with a novel Wt1 gene mutation.
    Machin GA.
    Birth Defects Orig Artic Ser; 1996 Mar 16; 30(1):269-86. PubMed ID: 9125334
    [No Abstract] [Full Text] [Related]

  • 29. Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS).
    Gbadegesin R, Hinkes BG, Hoskins BE, Vlangos CN, Heeringa SF, Liu J, Loirat C, Ozaltin F, Hashmi S, Ulmer F, Cleper R, Ettenger R, Antignac C, Wiggins RC, Zenker M, Hildebrandt F.
    Nephrol Dial Transplant; 2008 Apr 16; 23(4):1291-7. PubMed ID: 18065803
    [Abstract] [Full Text] [Related]

  • 30. [Clinical and pathological features of Denys-Drash syndrome: report of 3 cases].
    Wang HY, Sun LZ, Yue ZH, Yang J, Jiang XY, Mo Y.
    Zhonghua Er Ke Za Zhi; 2012 Nov 16; 50(11):855-8. PubMed ID: 23302619
    [Abstract] [Full Text] [Related]

  • 31. Wilms' tumour 1 gene mutations in south Indian children with steroid-resistant nephrotic syndrome.
    Kumar AS, Srilakshmi R, Karthickeyan S, Balakrishnan K, Padmaraj R, Senguttuvan P.
    Indian J Med Res; 2016 Aug 16; 144(2):276-280. PubMed ID: 27934809
    [Abstract] [Full Text] [Related]

  • 32. 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 16; 52(4):519-24. PubMed ID: 10762296
    [Abstract] [Full Text] [Related]

  • 33. 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]

  • 34. Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene.
    Köhler B, Schumacher V, Schulte-Overberg U, Biewald W, Lennert T, l'Allemand D, Royer-Pokora B, Grüters A.
    Pediatr Res; 1999 Feb 04; 45(2):187-90. PubMed ID: 10022588
    [Abstract] [Full Text] [Related]

  • 35. WT1 mutations may be a cause of severe renal failure due to nephroblastomatosis in Wilms' tumor patients.
    Santín S, Fraga G, Ruíz P, Pardo N, Torrent M, Martí T, Ballarín J, Ars E, Torra R.
    Clin Nephrol; 2011 Sep 04; 76(3):244-8. PubMed ID: 21888862
    [Abstract] [Full Text] [Related]

  • 36. A familial WT1 mutation associated with incomplete Denys-Drash syndrome.
    Zhu C, Zhao F, Zhang W, Wu H, Chen Y, Ding G, Zhang A, Huang S.
    Eur J Pediatr; 2013 Oct 04; 172(10):1357-62. PubMed ID: 23715653
    [Abstract] [Full Text] [Related]

  • 37. 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 04; 40(2):113-120. PubMed ID: 31707902
    [Abstract] [Full Text] [Related]

  • 38. A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X.
    Heathcott RW, Morison IM, Gubler MC, Corbett R, Reeve AE.
    Hum Mutat; 2002 Apr 04; 19(4):462. PubMed ID: 11933209
    [Abstract] [Full Text] [Related]

  • 39. Genetic Testing Proves Crucial in Case of Ambiguous Genitalia and Renal Masses.
    Weaver J, Rove KO, Meenakshi-Sundaram B, Vricella GJ.
    Urology; 2019 Jul 04; 129():194-196. PubMed ID: 30914336
    [Abstract] [Full Text] [Related]

  • 40. Isolated diffuse mesangial sclerosis and Wilms tumor suppressor gene.
    Ito S, Takata A, Hataya H, Ikeda M, Kikuchi H, Hata J, Honda M.
    J Pediatr; 2001 Mar 04; 138(3):425-7. PubMed ID: 11241056
    [Abstract] [Full Text] [Related]

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