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Journal Abstract Search

507 related items for PubMed ID: 12776285

  • 1. Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin.
    Bertelli R, Ginevri F, Caridi G, Dagnino M, Sandrini S, Di Duca M, Emma F, Sanna-Cherchi S, Scolari F, Neri TM, Murer L, Massella L, Basile G, Rizzoni G, Perfumo F, Ghiggeri GM.
    Am J Kidney Dis; 2003 Jun; 41(6):1314-21. PubMed ID: 12776285
    [Abstract] [Full Text] [Related]

  • 2. Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome.
    Carraro M, Caridi G, Bruschi M, Artero M, Bertelli R, Zennaro C, Musante L, Candiano G, Perfumo F, Ghiggeri GM.
    J Am Soc Nephrol; 2002 Jul; 13(7):1946-52. PubMed ID: 12089392
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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 27; 21(10):1476-9. PubMed ID: 16721582
    [Abstract] [Full Text] [Related]

  • 5. 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 27; 12(12):2742-2746. PubMed ID: 11729243
    [Abstract] [Full Text] [Related]

  • 6. Post-Transplant Recurrence of Focal Segmental Glomerulosclerosis in a Child With Heterozygous Mutations in NPHS1 and NPHS2.
    Battelino N, Arnol M, Kandus A, Ponikvar R, Novljan G.
    Ther Apher Dial; 2016 Jun 27; 20(3):312-7. PubMed ID: 27312921
    [Abstract] [Full Text] [Related]

  • 7. 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 27; 12(3):341-6. PubMed ID: 18208440
    [Abstract] [Full Text] [Related]

  • 8. 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 27; 44(2):e22-24. PubMed ID: 15264208
    [Abstract] [Full Text] [Related]

  • 9. 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 27; 19(5):561-4. PubMed ID: 15015071
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome.
    Oleggini R, Bertelli R, Di Donato A, Di Duca M, Caridi G, Sanna-Cherchi S, Scolari F, Murer L, Allegri L, Coppo R, Emma F, Camussi G, Perfumo F, Ghiggeri GM.
    Gene Expr; 2006 Sep 29; 13(1):59-66. PubMed ID: 16572591
    [Abstract] [Full Text] [Related]

  • 12. Soluble CD40 ligand directly alters glomerular permeability and may act as a circulating permeability factor in FSGS.
    Doublier S, Zennaro C, Musante L, Spatola T, Candiano G, Bruschi M, Besso L, Cedrino M, Carraro M, Ghiggeri GM, Camussi G, Lupia E.
    PLoS One; 2017 Sep 29; 12(11):e0188045. PubMed ID: 29155846
    [Abstract] [Full Text] [Related]

  • 13. Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis.
    Laurin LP, Lu M, Mottl AK, Blyth ER, Poulton CJ, Weck KE.
    Nephrol Dial Transplant; 2014 Nov 29; 29(11):2062-9. PubMed ID: 24500309
    [Abstract] [Full Text] [Related]

  • 14. Posttransplant recurrence of proteinuria in a case of focal segmental glomerulosclerosis associated with WT1 mutation.
    Ghiggeri GM, Aucella F, Caridi G, Bisceglia L, Ghio L, Gigante M, Perfumo F, Carraro M, Gesualdo L.
    Am J Transplant; 2006 Sep 29; 6(9):2208-11. PubMed ID: 16780544
    [Abstract] [Full Text] [Related]

  • 15. Podocin-related mechanisms in posttransplant [corrected] recurrence of focal segmental glomerulosclerosis [corrected].
    Caridi G, Dagnino M, Sanna-Cherchi S, Perfumo F, Ghiggeri GM.
    Transplant Proc; 2006 Dec 29; 38(10):3486-90. PubMed ID: 17175312
    [Abstract] [Full Text] [Related]

  • 16. Recurrent nephrotic syndrome in homozygous truncating NPHS2 mutation is not due to anti-podocin antibodies.
    Becker-Cohen R, Bruschi M, Rinat C, Feinstein S, Zennaro C, Ghiggeri GM, Frishberg Y.
    Am J Transplant; 2007 Jan 29; 7(1):256-60. PubMed ID: 17109732
    [Abstract] [Full Text] [Related]

  • 17. NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosis.
    Monteiro EJ, Pereira AC, Pereira AB, Krieger JE, Mastroianni-Kirsztajn G.
    J Nephrol; 2006 Jan 29; 19(3):366-71. PubMed ID: 16874699
    [Abstract] [Full Text] [Related]

  • 18. Effect of pre-and postoperative plasmapheresis on posttransplant recurrence of focal segmental glomerulosclerosis in children.
    Ohta T, Kawaguchi H, Hattori M, Komatsu Y, Akioka Y, Nagata M, Shiraga H, Ito K, Takahashi K, Ishikawa N, Tanabe K, Yamaguchi Y, Ota K.
    Transplantation; 2001 Mar 15; 71(5):628-33. PubMed ID: 11292291
    [Abstract] [Full Text] [Related]

  • 19. The podocin mutation R229Q and early recurrence (within the first year) of glomerular disease after renal transplantation.
    Mohey H, Thibaudin L, Laurent B, Berthoux F.
    Ann Transplant; 2013 Aug 28; 18():436-42. PubMed ID: 23982418
    [Abstract] [Full Text] [Related]

  • 20. Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.
    Jungraithmayr TC, Hofer K, Cochat P, Chernin G, Cortina G, Fargue S, Grimm P, Knueppel T, Kowarsch A, Neuhaus T, Pagel P, Pfeiffer KP, Schäfer F, Schönermarck U, Seeman T, Toenshoff B, Weber S, Winn MP, Zschocke J, Zimmerhackl LB.
    J Am Soc Nephrol; 2011 Mar 28; 22(3):579-85. PubMed ID: 21355056
    [Abstract] [Full Text] [Related]

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