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Journal Abstract Search

282 related items for PubMed ID: 24969201

  • 41. NPHS2 variation in focal and segmental glomerulosclerosis.
    Tonna SJ, Needham A, Polu K, Uscinski A, Appel GB, Falk RJ, Katz A, Al-Waheeb S, Kaplan BS, Jerums G, Savige J, Harmon J, Zhang K, Curhan GC, Pollak MR.
    BMC Nephrol; 2008 Sep 29; 9():13. PubMed ID: 18823551
    [Abstract] [Full Text] [Related]

  • 42. [NPHS2 Mutation analysis study in children with steroid-resistant nephrotic syndrome].
    Azocar M, Vega Á, Farfán M, Cano F.
    Rev Chil Pediatr; 2016 Sep 29; 87(1):31-6. PubMed ID: 26455708
    [Abstract] [Full Text] [Related]

  • 43. Three siblings with steroid-resistant nephrotic syndrome: new NPHS2 mutations in a Turkish family.
    Ekim M, Ozçakar ZB, Acar B, Yüksel S, Yalçnkaya F, Tulunay O, Ensari A, Erbay B.
    Am J Kidney Dis; 2004 Aug 29; 44(2):e22-24. PubMed ID: 15264208
    [Abstract] [Full Text] [Related]

  • 44. Cyclosporine A responsive congenital nephrotic syndrome with single heterozygous variants in NPHS1, NPHS2, and PLCE1.
    Eichinger A, Ponsel S, Bergmann C, Günthner R, Hoefele J, Amann K, Lange-Sperandio B.
    Pediatr Nephrol; 2018 Jul 29; 33(7):1269-1272. PubMed ID: 29663071
    [Abstract] [Full Text] [Related]

  • 45. [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 29; 42(2):108-12. PubMed ID: 15059485
    [Abstract] [Full Text] [Related]

  • 46. NPHS2 gene mutations in azerbaijani children with steroid-resistant nephrotic syndrome.
    Baylarov R, Senol O, Atan M, Berdeli A.
    Saudi J Kidney Dis Transpl; 2020 Feb 29; 31(1):144-149. PubMed ID: 32129207
    [Abstract] [Full Text] [Related]

  • 47. NPHS2 mutation associated with recurrence of proteinuria after transplantation.
    Billing H, Müller D, Ruf R, Lichtenberger A, Hildebrandt F, August C, Querfeld U, Haffner D.
    Pediatr Nephrol; 2004 May 29; 19(5):561-4. PubMed ID: 15015071
    [Abstract] [Full Text] [Related]

  • 48. R229Q polymorphism of NPHS2 gene in patients with late-onset steroid-resistance nephrotic syndrome: a preliminary study.
    Fotouhi N, Ardalan M, Jabbarpour Bonyadi M, Abdolmohammadi R, Kamalifar A, Nasri H, Einollahi B.
    Iran J Kidney Dis; 2013 Sep 29; 7(5):399-403. PubMed ID: 24072153
    [Abstract] [Full Text] [Related]

  • 49. Familial focal segmental glomerulosclerosis (FSGS) in a Nigerian family and exclusion of mutations in NPHS2,WT1 and APOL1.
    Anochie IC, Eke FU, Okpere AN.
    West Afr J Med; 2012 Sep 29; 31(4):273-6. PubMed ID: 23468032
    [Abstract] [Full Text] [Related]

  • 50. Advances in molecular diagnosis and therapeutics in nephrotic syndrome and focal and segmental glomerulosclerosis.
    Sharif B, Barua M.
    Curr Opin Nephrol Hypertens; 2018 May 29; 27(3):194-200. PubMed ID: 29465426
    [Abstract] [Full Text] [Related]

  • 51. Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.
    Wang F, Zhang Y, Mao J, Yu Z, Yi Z, Yu L, Sun J, Wei X, Ding F, Zhang H, Xiao H, Yao Y, Tan W, Lovric S, Ding J, Hildebrandt F.
    Pediatr Nephrol; 2017 Jul 29; 32(7):1181-1192. PubMed ID: 28204945
    [Abstract] [Full Text] [Related]

  • 52. 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 29; 7(5):357-62. PubMed ID: 24072147
    [Abstract] [Full Text] [Related]

  • 53. 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 29; 23(3):421-7. PubMed ID: 18058136
    [Abstract] [Full Text] [Related]

  • 54. Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic Counseling.
    Rood IM, Deegens JKJ, Lugtenberg D, Bongers EMHF, Wetzels JFM.
    Am J Kidney Dis; 2019 Mar 29; 73(3):400-403. PubMed ID: 30241959
    [Abstract] [Full Text] [Related]

  • 55. Recurrence of focal-segmental glomerulosclerosis in children after renal transplantation: clinical and genetic aspects.
    Weber S, Tönshoff B.
    Transplantation; 2005 Sep 27; 80(1 Suppl):S128-34. PubMed ID: 16286890
    [Abstract] [Full Text] [Related]

  • 56. 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]

  • 57. 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 24; 3(2):99-102. PubMed ID: 19395786
    [Abstract] [Full Text] [Related]

  • 58. Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseases.
    Di Duca M, Oleggini R, Sanna-Cherchi S, Pasquali L, Di Donato A, Parodi S, Bertelli R, Caridi G, Frasca G, Cerullo G, Amoroso A, Schena FP, Scolari F, Ghiggeri GM, European IgA Nephropathy Consortium.
    Kidney Int; 2006 Oct 24; 70(7):1332-41. PubMed ID: 16900088
    [Abstract] [Full Text] [Related]

  • 59. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity.
    Bullich G, Trujillano D, Santín S, Ossowski S, Mendizábal S, Fraga G, Madrid Á, Ariceta G, Ballarín J, Torra R, Estivill X, Ars E.
    Eur J Hum Genet; 2015 Sep 24; 23(9):1192-9. PubMed ID: 25407002
    [Abstract] [Full Text] [Related]

  • 60. Prevalence of the NPHS2 variants p.R229Q, p.A242V, and p.R138Q in patients with focal segmental glomerulosclerosis.
    de Almeida R, da Silva WC, Garbin HI, Itaquy TP, Dos Santos Pereira F, Garcia CD, Keitel E, Sales Luiz Vianna F, Veronese FV.
    Clin Nephrol; 2020 Oct 24; 94(4):187-196. PubMed ID: 32691731
    [Abstract] [Full Text] [Related]

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