These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

229 related items for PubMed ID: 27934809

  • 1. 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; 144(2):276-280. PubMed ID: 27934809
    [Abstract] [Full Text] [Related]

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

  • 3. 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]

  • 4. 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]

  • 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 04; 21(10):1393-8. PubMed ID: 16909243
    [Abstract] [Full Text] [Related]

  • 6. Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa.
    Nandlal L, Winkler CA, Bhimma R, Cho S, Nelson GW, Haripershad S, Naicker T.
    Eur J Pediatr; 2022 Oct 04; 181(10):3595-3606. PubMed ID: 35920919
    [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. 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 04; 57(5):1868-72. PubMed ID: 10792605
    [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, Guan N, Fan QF, Zhang HW.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Dec 11; 32(6):949-57. PubMed ID: 18182709
    [Abstract] [Full Text] [Related]

  • 11. Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
    Chernin G, Heeringa SF, Gbadegesin R, Liu J, Hinkes BG, Vlangos CN, Vega-Warner V, Hildebrandt F.
    Pediatr Nephrol; 2008 Sep 11; 23(9):1455-60. PubMed ID: 18543005
    [Abstract] [Full Text] [Related]

  • 12. Glomerular Transcriptome Profiles in Focal Glomerulosclerosis: New Genes and Pathways for Steroid Resistance.
    Tong J, Jin Y, Weng Q, Yu S, Jafar Hussain HM, Ren H, Xu J, Zhang W, Li X, Wang W, Xie J, Chen N.
    Am J Nephrol; 2020 Sep 11; 51(6):442-452. PubMed ID: 32348995
    [Abstract] [Full Text] [Related]

  • 13. TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.
    Gigante M, Caridi G, Montemurno E, Soccio M, d'Apolito M, Cerullo G, Aucella F, Schirinzi A, Emma F, Massella L, Messina G, De Palo T, Ranieri E, Ghiggeri GM, Gesualdo L.
    Clin J Am Soc Nephrol; 2011 Jul 11; 6(7):1626-34. PubMed ID: 21734084
    [Abstract] [Full Text] [Related]

  • 14. Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.
    Bińczak-Kuleta A, Rubik J, Litwin M, Ryder M, Lewandowska K, Taryma-Leśniak O, Clark JS, Grenda R, Ciechanowicz A.
    Bosn J Basic Med Sci; 2014 May 11; 14(2):89-93. PubMed ID: 24856380
    [Abstract] [Full Text] [Related]

  • 15. Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations.
    Gellermann J, Stefanidis CJ, Mitsioni A, Querfeld U.
    Pediatr Nephrol; 2010 Jul 11; 25(7):1285-9. PubMed ID: 20191369
    [Abstract] [Full Text] [Related]

  • 16. 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 11; 32(1):81-89. PubMed ID: 27300205
    [Abstract] [Full Text] [Related]

  • 17. WT1 and NPHS2 mutations in Korean children with steroid-resistant nephrotic syndrome.
    Cho HY, Lee JH, Choi HJ, Lee BH, Ha IS, Choi Y, Cheong HI.
    Pediatr Nephrol; 2008 Jan 11; 23(1):63-70. PubMed ID: 17934764
    [Abstract] [Full Text] [Related]

  • 18. [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]

  • 19. 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 11; 59(2):325-31. PubMed ID: 16439601
    [Abstract] [Full Text] [Related]

  • 20. Eye involvement in children with primary focal segmental glomerulosclerosis.
    Ozaltin F, Heeringa S, Poyraz CE, Bilginer Y, Kadayifcilar S, Besbas N, Topaloglu R, Ozen S, Hildebrandt F, Bakkaloglu A.
    Pediatr Nephrol; 2008 Mar 11; 23(3):421-7. PubMed ID: 18058136
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.