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540 related items for PubMed ID: 15253707

  • 1. Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.
    Ruf RG, Schultheiss M, Lichtenberger A, Karle SM, Zalewski I, Mucha B, Everding AS, Neuhaus T, Patzer L, Plank C, Haas JP, Ozaltin F, Imm A, Fuchshuber A, Bakkaloglu A, Hildebrandt F, APN Study Group.
    Kidney Int; 2004 Aug; 66(2):564-70. PubMed ID: 15253707
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.
    Mucha B, Ozaltin F, Hinkes BG, Hasselbacher K, Ruf RG, Schultheiss M, Hangan D, Hoskins BE, Everding AS, Bogdanovic R, Seeman T, Hoppe B, Hildebrandt F, Members of the APN Study Group.
    Pediatr Res; 2006 Feb 04; 59(2):325-31. PubMed ID: 16439601
    [Abstract] [Full Text] [Related]

  • 4. 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 04; 85(5):1169-78. PubMed ID: 24402088
    [Abstract] [Full Text] [Related]

  • 5. 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 04; 426(1-2):177-181. PubMed ID: 27885584
    [Abstract] [Full Text] [Related]

  • 6. Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy.
    Ahn YH, Park EJ, Kang HG, Kim SH, Cho HY, Shin JI, Lee JH, Park YS, Kim KS, Ha IS, Cheong HI.
    Pediatr Nephrol; 2017 Jan 04; 32(1):81-89. PubMed ID: 27300205
    [Abstract] [Full Text] [Related]

  • 7. Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms' tumor 1 (WT1) gene.
    Megremis S, Mitsioni A, Fylaktou I, Tzeli SK, Komianou F, Stefanidis CJ, Kanavakis E, Traeger-Synodinos J.
    Eur J Pediatr; 2011 Dec 04; 170(12):1529-34. PubMed ID: 21499692
    [Abstract] [Full Text] [Related]

  • 8. 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 04; 32(6):949-57. PubMed ID: 18182709
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. [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 11; 46(9):692-7. PubMed ID: 19099861
    [Abstract] [Full Text] [Related]

  • 11. 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 11; 144(2):276-280. PubMed ID: 27934809
    [Abstract] [Full Text] [Related]

  • 12. 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 11; 21(10):1393-8. PubMed ID: 16909243
    [Abstract] [Full Text] [Related]

  • 13. Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome.
    Gbadegesin R, Hinkes B, Vlangos C, Mucha B, Liu J, Hopcian J, Hildebrandt F.
    Pediatr Nephrol; 2007 Apr 11; 22(4):509-13. PubMed ID: 17216259
    [Abstract] [Full Text] [Related]

  • 14. Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.
    Ruf RG, Lichtenberger A, Karle SM, Haas JP, Anacleto FE, Schultheiss M, Zalewski I, Imm A, Ruf EM, Mucha B, Bagga A, Neuhaus T, Fuchshuber A, Bakkaloglu A, Hildebrandt F, Arbeitsgemeinschaft Für Pädiatrische Nephrologie Study Group.
    J Am Soc Nephrol; 2004 Mar 11; 15(3):722-32. PubMed ID: 14978175
    [Abstract] [Full Text] [Related]

  • 15. Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome.
    Büscher AK, Beck BB, Melk A, Hoefele J, Kranz B, Bamborschke D, Baig S, Lange-Sperandio B, Jungraithmayr T, Weber LT, Kemper MJ, Tönshoff B, Hoyer PF, Konrad M, Weber S, German Pediatric Nephrology Association (GPN).
    Clin J Am Soc Nephrol; 2016 Feb 05; 11(2):245-53. PubMed ID: 26668027
    [Abstract] [Full Text] [Related]

  • 16. 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 05; 63(11):104047. PubMed ID: 32891756
    [Abstract] [Full Text] [Related]

  • 17. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).
    Hinkes BG, Mucha B, Vlangos CN, Gbadegesin R, Liu J, Hasselbacher K, Hangan D, Ozaltin F, Zenker M, Hildebrandt F, Arbeitsgemeinschaft für Paediatrische Nephrologie Study Group.
    Pediatrics; 2007 Apr 05; 119(4):e907-19. PubMed ID: 17371932
    [Abstract] [Full Text] [Related]

  • 18. Screening of WT1 mutations in exon 8 and 9 in children with steroid resistant nephrotic syndrome from a single centre and establishment of a rapid screening assay using high-resolution melting analysis in a clinical setting.
    Siji A, Pardeshi VC, Ravindran S, Vasudevan A, Vasudevan A.
    BMC Med Genet; 2017 Jan 10; 18(1):3. PubMed ID: 28068926
    [Abstract] [Full Text] [Related]

  • 19. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
    Weber S, Gribouval O, Esquivel EL, Morinière V, Tête MJ, Legendre C, Niaudet P, Antignac C.
    Kidney Int; 2004 Aug 10; 66(2):571-9. PubMed ID: 15253708
    [Abstract] [Full Text] [Related]

  • 20. TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome.
    Mir S, Yavascan O, Berdeli A, Sozeri B.
    Nephrol Dial Transplant; 2012 Jan 10; 27(1):205-9. PubMed ID: 21511817
    [Abstract] [Full Text] [Related]

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