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Journal Abstract Search

450 related items for PubMed ID: 15780077

  • 1. 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]

  • 2. 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; 119(4):e907-19. PubMed ID: 17371932
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. [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]

  • 5. 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 Feb; 99(2):c31-6. PubMed ID: 15627790
    [Abstract] [Full Text] [Related]

  • 6. 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]

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

  • 8. Molecular basis of steroid-resistant nephrotic syndrome.
    Antignac C.
    Nefrologia; 2005 Sep 29; 25 Suppl 2():25-8. PubMed ID: 16050398
    [Abstract] [Full Text] [Related]

  • 9. 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 29; 14(2):89-93. PubMed ID: 24856380
    [Abstract] [Full Text] [Related]

  • 10. Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.
    Koziell A, Grech V, Hussain S, Lee G, Lenkkeri U, Tryggvason K, Scambler P.
    Hum Mol Genet; 2002 Feb 15; 11(4):379-88. PubMed ID: 11854170
    [Abstract] [Full Text] [Related]

  • 11. A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
    Abid A, Khaliq S, Shahid S, Lanewala A, Mubarak M, Hashmi S, Kazi J, Masood T, Hafeez F, Naqvi SA, Rizvi SA, Mehdi SQ.
    Gene; 2012 Jul 10; 502(2):133-7. PubMed ID: 22565185
    [Abstract] [Full Text] [Related]

  • 12. Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.
    Machuca E, Benoit G, Nevo F, Tête MJ, Gribouval O, Pawtowski A, Brandström P, Loirat C, Niaudet P, Gubler MC, Antignac C.
    J Am Soc Nephrol; 2010 Jul 10; 21(7):1209-17. PubMed ID: 20507940
    [Abstract] [Full Text] [Related]

  • 13. The Role of p.Ser1105Ser (in NPHS1 Gene) and p.Arg548Leu (in PLCE1 Gene) with Disease Status of Vietnamese Patients with Congenital Nephrotic Syndrome: Benign or Pathogenic?
    Thi Kim Lien N, Van Dem P, Thu Huong N, Minh Dien T, Thi Thu Thuy T, Van Tung N, Huy Hoang N, Thi Quynh Huong N.
    Medicina (Kaunas); 2019 Apr 12; 55(4):. PubMed ID: 31013750
    [Abstract] [Full Text] [Related]

  • 14. Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome.
    Li GM, Cao Q, Shen Q, Sun L, Zhai YH, Liu HM, An Y, Xu H.
    BMC Nephrol; 2018 Dec 29; 19(1):382. PubMed ID: 30594156
    [Abstract] [Full Text] [Related]

  • 15. 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 29; 21(4):677-684. PubMed ID: 27573339
    [Abstract] [Full Text] [Related]

  • 16. [NPHS1 mutations in a Chinese family with congenital nephrotic syndrome].
    Shi Y, Ding J, Liu JC, Wang H, Bu DF.
    Zhonghua Er Ke Za Zhi; 2005 Nov 29; 43(11):805-9. PubMed ID: 16316524
    [Abstract] [Full Text] [Related]

  • 17. NPHS1 gene mutation in Japanese patients with congenital nephrotic syndrome.
    Aya K, Shimizu J, Ohtomo Y, Satomura K, Suzuki H, Yan K, Sado Y, Morishima T, Tanaka H.
    Nephrol Dial Transplant; 2009 Aug 29; 24(8):2411-4. PubMed ID: 19321760
    [Abstract] [Full Text] [Related]

  • 18. Novel mutations in steroid-resistant nephrotic syndrome diagnosed in Tunisian children.
    Mbarek IB, Abroug S, Omezzine A, Pawtowski A, Gubler MC, Bouslama A, Harbi A, Antignac C.
    Pediatr Nephrol; 2011 Feb 29; 26(2):241-9. PubMed ID: 21125408
    [Abstract] [Full Text] [Related]

  • 19. 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 29; 426(1-2):177-181. PubMed ID: 27885584
    [Abstract] [Full Text] [Related]

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