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Journal Abstract Search

335 related items for PubMed ID: 15059485

  • 1. [A novel mutation of NPHS2 identified in a Chinese family with steroid-resistant nephrotic syndrome].
    Yu ZH, Ding J, Guan N, Shi Y, Zhang JJ, Huang JP, Yao Y, Yang JY.
    Zhonghua Er Ke Za Zhi; 2004 Feb; 42(2):108-12. PubMed ID: 15059485
    [Abstract] [Full Text] [Related]

  • 2. A novel mutation of NPHS2 identified in a Chinese family.
    Yu Z, Ding J, Guan N, Shi Y, Zhang J, Huang J, Yao Y, Yang J.
    Pediatr Nephrol; 2004 Nov; 19(11):1285-9. PubMed ID: 15322893
    [Abstract] [Full Text] [Related]

  • 3. In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutation.
    Zhang SY, Marlier A, Gribouval O, Gilbert T, Heidet L, Antignac C, Gubler MC.
    Kidney Int; 2004 Sep; 66(3):945-54. PubMed ID: 15327385
    [Abstract] [Full Text] [Related]

  • 4. [Mutations in NPHS2 in familial steroid-resistant nephrotic syndrome in Southern Chinese Han ethnic group].
    Fu R, Chen XM, Wang QH, Chen SP, Yu ZH, Ye LY, Ren RN, Huang J, Wang CF.
    Zhonghua Er Ke Za Zhi; 2008 Aug; 46(8):591-6. PubMed ID: 19099831
    [Abstract] [Full Text] [Related]

  • 5. Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome.
    Sako M, Nakanishi K, Obana M, Yata N, Hoshii S, Takahashi S, Wada N, Takahashi Y, Kaku Y, Satomura K, Ikeda M, Honda M, Iijima K, Yoshikawa N.
    Kidney Int; 2005 Apr; 67(4):1248-55. PubMed ID: 15780077
    [Abstract] [Full Text] [Related]

  • 6. A novel mutation in NPHS2 gene identified in a Chinese pedigree with autosomal recessive steroid-resistant nephrotic syndrome.
    Sun H, Zhou W, Wang J, Yin L, Lu Y, Fu Q.
    Pathology; 2009 Apr; 41(7):661-5. PubMed ID: 20001346
    [Abstract] [Full Text] [Related]

  • 7. [NPHS2 Mutation analysis study in children with steroid-resistant nephrotic syndrome].
    Azocar M, Vega Á, Farfán M, Cano F.
    Rev Chil Pediatr; 2016 Apr; 87(1):31-6. PubMed ID: 26455708
    [Abstract] [Full Text] [Related]

  • 8. Novel NPHS2 variant in patients with familial steroid-resistant nephrotic syndrome with early onset, slow progression and dominant inheritance pattern.
    Suvanto M, Patrakka J, Jahnukainen T, Sjöström PM, Nuutinen M, Arikoski P, Kataja J, Kestilä M, Jalanko H.
    Clin Exp Nephrol; 2017 Aug; 21(4):677-684. PubMed ID: 27573339
    [Abstract] [Full Text] [Related]

  • 9. [Heterozygotic mutation in NPHS2 gene as a cause of familial steroid resistant nephrotic syndrome in two siblings--case report].
    Drozdz D, Pietrzyk JA, Wierzchowska-Słowiaczek E, Sancewicz-Pach K, Antignac C, Miezyński W.
    Przegl Lek; 2006 Aug; 63 Suppl 3():85-6. PubMed ID: 16898497
    [Abstract] [Full Text] [Related]

  • 10. A novel NPHS2 mutation (c.865A > G) identified in a Chinese family with steroid-resistant nephrotic syndrome alters subcellular localization of nephrin.
    Wu N, Zhu Y, Jiang W, Song Y, Yin L, Lu Y, Tao D, Liu Y, Ma Y.
    Genes Genomics; 2022 May; 44(5):551-559. PubMed ID: 35099763
    [Abstract] [Full Text] [Related]

  • 11. Mutations in NPHS2 in sporadic steroid-resistant nephrotic syndrome in Chinese children.
    Yu Z, Ding J, Huang J, Yao Y, Xiao H, Zhang J, Liu J, Yang J.
    Nephrol Dial Transplant; 2005 May; 20(5):902-8. PubMed ID: 15769810
    [Abstract] [Full Text] [Related]

  • 12. NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children.
    Maruyama K, Iijima K, Ikeda M, Kitamura A, Tsukaguchi H, Yoshiya K, Hoshii S, Wada N, Uemura O, Satomura K, Honda M, Yoshikawa N.
    Pediatr Nephrol; 2003 May; 18(5):412-6. PubMed ID: 12687458
    [Abstract] [Full Text] [Related]

  • 13. Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children.
    Frishberg Y, Rinat C, Megged O, Shapira E, Feinstein S, Raas-Rothschild A.
    J Am Soc Nephrol; 2002 Feb; 13(2):400-405. PubMed ID: 11805168
    [Abstract] [Full Text] [Related]

  • 14. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome.
    Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler MC, Niaudet P, Antignac C.
    Nat Genet; 2000 Apr; 24(4):349-54. PubMed ID: 10742096
    [Abstract] [Full Text] [Related]

  • 15. Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
    Dhandapani MC, Venkatesan V, Rengaswamy NB, Gowrishankar K, Ekambaram S, Sengutavan P, Perumal V.
    Clin Exp Nephrol; 2017 Feb; 21(1):127-133. PubMed ID: 26820844
    [Abstract] [Full Text] [Related]

  • 16. NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.
    Berdeli A, Mir S, Yavascan O, Serdaroglu E, Bak M, Aksu N, Oner A, Anarat A, Donmez O, Yildiz N, Sever L, Tabel Y, Dusunsel R, Sonmez F, Cakar N.
    Pediatr Nephrol; 2007 Dec; 22(12):2031-40. PubMed ID: 17899208
    [Abstract] [Full Text] [Related]

  • 17. Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome.
    Megremis S, Mitsioni A, Mitsioni AG, Fylaktou I, Kitsiou-Tzelli S, Stefanidis CJ, Kanavakis E, Traeger-Synodinos J.
    Genet Test Mol Biomarkers; 2009 Apr; 13(2):249-56. PubMed ID: 19371226
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
    Lipska BS, Iatropoulos P, Maranta R, Caridi G, Ozaltin F, Anarat A, Balat A, Gellermann J, Trautmann A, Erdogan O, Saeed B, Emre S, Bogdanovic R, Azocar M, Balasz-Chmielewska I, Benetti E, Caliskan S, Mir S, Melk A, Ertan P, Baskin E, Jardim H, Davitaia T, Wasilewska A, Drozdz D, Szczepanska M, Jankauskiene A, Higuita LM, Ardissino G, Ozkaya O, Kuzma-Mroczkowska E, Soylemezoglu O, Ranchin B, Medynska A, Tkaczyk M, Peco-Antic A, Akil I, Jarmolinski T, Firszt-Adamczyk A, Dusek J, Simonetti GD, Gok F, Gheissari A, Emma F, Krmar RT, Fischbach M, Printza N, Simkova E, Mele C, Ghiggeri GM, Schaefer F, PodoNet Consortium.
    Kidney Int; 2013 Jul; 84(1):206-13. PubMed ID: 23515051
    [Abstract] [Full Text] [Related]

  • 20. 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; 22(4):509-13. PubMed ID: 17216259
    [Abstract] [Full Text] [Related]

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