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Journal Abstract Search

454 related items for PubMed ID: 24500309

  • 21. 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; 66(2):571-9. PubMed ID: 15253708
    [Abstract] [Full Text] [Related]

  • 22. NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosis.
    Monteiro EJ, Pereira AC, Pereira AB, Krieger JE, Mastroianni-Kirsztajn G.
    J Nephrol; 2006 Aug; 19(3):366-71. PubMed ID: 16874699
    [Abstract] [Full Text] [Related]

  • 23. Clinical features and mutational survey of NPHS2 (podocin) in Japanese children with focal segmental glomerulosclerosis who underwent renal transplantation.
    Furue T, Hattori M, Tsukaguchi H, Kitamura A, Oomori T, Ogino D, Nakakura H, Ashida A, Miura K, Hisano M, Takahashi K, Chikamoto H, Akioka Y, Sakano T.
    Pediatr Transplant; 2008 May; 12(3):341-6. PubMed ID: 18208440
    [Abstract] [Full Text] [Related]

  • 24. mRNA sequencing of a novel NPHS2 intronic mutation in a child with focal and segmental glomerulosclerosis.
    Benetti E, Caridi G, Centi S, Vella MD, Ghiggeri GM, Artifoni L, Murer L.
    Saudi J Kidney Dis Transpl; 2014 Jul; 25(4):854-7. PubMed ID: 24969201
    [Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. Recurrence of proteinuria 10 years post-transplant in NPHS2-associated focal segmental glomerulosclerosis after conversion from cyclosporin A to sirolimus.
    Höcker B, Knüppel T, Waldherr R, Schaefer F, Weber S, Tönshoff B.
    Pediatr Nephrol; 2006 Oct; 21(10):1476-9. PubMed ID: 16721582
    [Abstract] [Full Text] [Related]

  • 27. APOL1 risk genotype in European steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis patients of different African ancestries.
    Gribouval O, Boyer O, Knebelmann B, Karras A, Dantal J, Fourrage C, Alibeu O, Hogan J, Dossier C, Tête MJ, Antignac C, Servais A.
    Nephrol Dial Transplant; 2019 Nov 01; 34(11):1885-1893. PubMed ID: 29992269
    [Abstract] [Full Text] [Related]

  • 28. [A genetic viewpoint of focal glomerular sclerosis: fom genes to glomerular pathophysiology [corrected]].
    Aucella F, Bisceglia L, Stallone C.
    G Ital Nefrol; 2003 Nov 01; 20(4):356-67. PubMed ID: 14523896
    [Abstract] [Full Text] [Related]

  • 29. Genetic basis of nephrotic syndrome--review.
    Obeidová H, Merta M, Reiterová J, Maixnerová D, Stekrová J, Rysavá R, Tesar V.
    Prague Med Rep; 2006 Nov 01; 107(1):5-16. PubMed ID: 16752799
    [Abstract] [Full Text] [Related]

  • 30. 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 01; 23(9):1455-60. PubMed ID: 18543005
    [Abstract] [Full Text] [Related]

  • 31. Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.
    Reiterová J, Safránková H, Obeidová L, Stěkrová J, Maixnerová D, Merta M, Tesař V.
    Folia Biol (Praha); 2012 Sep 01; 58(2):64-8. PubMed ID: 22578956
    [Abstract] [Full Text] [Related]

  • 32. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review.
    Franceschini N, North KE, Kopp JB, McKenzie L, Winkler C.
    Genet Med; 2006 Feb 01; 8(2):63-75. PubMed ID: 16481888
    [Abstract] [Full Text] [Related]

  • 33. Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome.
    Boyer O, Benoit G, Gribouval O, Nevo F, Pawtowski A, Bilge I, Bircan Z, Deschênes G, Guay-Woodford LM, Hall M, Macher MA, Soulami K, Stefanidis CJ, Weiss R, Loirat C, Gubler MC, Antignac C.
    J Med Genet; 2010 Jul 01; 47(7):445-52. PubMed ID: 20591883
    [Abstract] [Full Text] [Related]

  • 34. Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.
    Caridi G, Bertelli R, Carrea A, Di Duca M, Catarsi P, Artero M, Carraro M, Zennaro C, Candiano G, Musante L, Seri M, Ginevri F, Perfumo F, Ghiggeri GM.
    J Am Soc Nephrol; 2001 Dec 01; 12(12):2742-2746. PubMed ID: 11729243
    [Abstract] [Full Text] [Related]

  • 35. 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 01; 84(1):206-13. PubMed ID: 23515051
    [Abstract] [Full Text] [Related]

  • 36. A comprehensive analysis of NPHS1 gene mutations in patients with sporadic focal segmental glomerulosclerosis.
    Zhuo L, Huang L, Yang Z, Li G, Wang L.
    BMC Med Genet; 2019 Jun 19; 20(1):111. PubMed ID: 31216994
    [Abstract] [Full Text] [Related]

  • 37. 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 19; 13(2):400-405. PubMed ID: 11805168
    [Abstract] [Full Text] [Related]

  • 38. TRPC6 and FSGS: the latest TRP channelopathy.
    Mukerji N, Damodaran TV, Winn MP.
    Biochim Biophys Acta; 2007 Aug 19; 1772(8):859-68. PubMed ID: 17459670
    [Abstract] [Full Text] [Related]

  • 39. Truncating Wilms Tumor Suppressor Gene 1 Mutation in an XX Female with Adult-Onset Focal Segmental Glomerulosclerosis and Streak Ovaries: A Case Report.
    Hoefele J, Kemper MJ, Schoenermarck U, Mueller S, Klein HG, Lemke A.
    Nephron; 2017 Aug 19; 135(1):72-76. PubMed ID: 27701157
    [Abstract] [Full Text] [Related]

  • 40. The podocin V260E mutation predicts steroid resistant nephrotic syndrome in black South African children with focal segmental glomerulosclerosis.
    Govender MA, Fabian J, Gottlich E, Levy C, Moonsamy G, Maher H, Winkler CA, Ramsay M.
    Commun Biol; 2019 Aug 19; 2():416. PubMed ID: 31754646
    [Abstract] [Full Text] [Related]

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