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Journal Abstract Search

330 related items for PubMed ID: 15059485

  • 21. 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; 23(9):1455-60. PubMed ID: 18543005
    [Abstract] [Full Text] [Related]

  • 22. Characterization of NPHS2 gene polymorphisms associated to steroid resistance nephrotic syndrome in Indian children.
    Joshi BB, Mistry KN, Gang S, Koringa PG, Joshi CG.
    Gene; 2017 Sep 10; 628():134-140. PubMed ID: 28712774
    [Abstract] [Full Text] [Related]

  • 23. NPHS2 mutations in children with steroid-resistant nephrotic syndrome.
    Otukesh H, Ghazanfari B, Fereshtehnejad SM, Bakhshayesh M, Hashemi M, Hoseini R, Chalian M, Salami A, Mehdipor L, Rahiminia A.
    Iran J Kidney Dis; 2009 Apr 10; 3(2):99-102. PubMed ID: 19395786
    [Abstract] [Full Text] [Related]

  • 24. 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 10; 15(3):722-32. PubMed ID: 14978175
    [Abstract] [Full Text] [Related]

  • 25. Genetic mutation in Egyptian children with steroid-resistant nephrotic syndrome.
    Thomas MM, Abdel-Hamid MS, Mahfouz NN, Ghobrial EE.
    J Formos Med Assoc; 2018 Jan 10; 117(1):48-53. PubMed ID: 28385484
    [Abstract] [Full Text] [Related]

  • 26. 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]

  • 27. Molecular basis of steroid-resistant nephrotic syndrome.
    Antignac C.
    Nefrologia; 2005 Aug 10; 25 Suppl 2():25-8. PubMed ID: 16050398
    [Abstract] [Full Text] [Related]

  • 28. NPHS2 gene in steroid-resistant nephrotic syndrome: prevalence, clinical course, and mutational spectrum in South-West Iranian children.
    Basiratnia M, Yavarian M, Torabinezhad S, Erjaee A.
    Iran J Kidney Dis; 2013 Sep 10; 7(5):357-62. PubMed ID: 24072147
    [Abstract] [Full Text] [Related]

  • 29. Disease-causing missense mutations in NPHS2 gene alter normal nephrin trafficking to the plasma membrane.
    Nishibori Y, Liu L, Hosoyamada M, Endou H, Kudo A, Takenaka H, Higashihara E, Bessho F, Takahashi S, Kershaw D, Ruotsalainen V, Tryggvason K, Khoshnoodi J, Yan K.
    Kidney Int; 2004 Nov 10; 66(5):1755-65. PubMed ID: 15496146
    [Abstract] [Full Text] [Related]

  • 30. 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 10; 181(10):3595-3606. PubMed ID: 35920919
    [Abstract] [Full Text] [Related]

  • 31. 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 10; 32(6):949-57. PubMed ID: 18182709
    [Abstract] [Full Text] [Related]

  • 32. 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 10; 14(2):89-93. PubMed ID: 24856380
    [Abstract] [Full Text] [Related]

  • 33. Molecular analysis of NPHS2 and ACTN4 genes in a series of 33 Italian patients affected by adult-onset nonfamilial focal segmental glomerulosclerosis.
    Aucella F, De Bonis P, Gatta G, Muscarella LA, Vigilante M, di Giorgio G, D'Errico M, Zelante L, Stallone C, Bisceglia L.
    Nephron Clin Pract; 2005 May 10; 99(2):c31-6. PubMed ID: 15627790
    [Abstract] [Full Text] [Related]

  • 34. 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 10; 6(7):1626-34. PubMed ID: 21734084
    [Abstract] [Full Text] [Related]

  • 35. NPHS2 mutations account for only 15% of nephrotic syndrome cases.
    Guaragna MS, Lutaif AC, Piveta CS, Souza ML, de Souza SR, Henriques TB, Maciel-Guerra AT, Belangero VM, Guerra-Junior G, De Mello MP.
    BMC Med Genet; 2015 Sep 29; 16():88. PubMed ID: 26420286
    [Abstract] [Full Text] [Related]

  • 36. NPHS1 and NPHS2 gene mutations in Chinese children with sporadic nephrotic syndrome.
    Mao J, Zhang Y, Du L, Dai Y, Gu W, Liu A, Shang S, Liang L.
    Pediatr Res; 2007 Jan 29; 61(1):117-22. PubMed ID: 17211152
    [Abstract] [Full Text] [Related]

  • 37. Genetic basis of nephrotic syndrome--review.
    Obeidová H, Merta M, Reiterová J, Maixnerová D, Stekrová J, Rysavá R, Tesar V.
    Prague Med Rep; 2006 Jan 29; 107(1):5-16. PubMed ID: 16752799
    [Abstract] [Full Text] [Related]

  • 38. Mutations in NPHS2 (podocin) in Mexican children with nephrotic syndrome who respond to standard steroid treatment.
    Carrasco-Miranda JS, Garcia-Alvarez R, Sotelo-Mundo RR, Valenzuela O, Islas-Osuna MA, Sotelo-Cruz N.
    Genet Mol Res; 2013 Jun 24; 12(2):2102-7. PubMed ID: 23913389
    [Abstract] [Full Text] [Related]

  • 39. 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 24; 119(4):e907-19. PubMed ID: 17371932
    [Abstract] [Full Text] [Related]

  • 40. Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome.
    Karle SM, Uetz B, Ronner V, Glaeser L, Hildebrandt F, Fuchshuber A.
    J Am Soc Nephrol; 2002 Feb 24; 13(2):388-393. PubMed ID: 11805166
    [Abstract] [Full Text] [Related]

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