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Journal Abstract Search

201 related items for PubMed ID: 15015071

  • 1. 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; 19(5):561-4. PubMed ID: 15015071
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 4. 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]

  • 5. 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 27; 41(6):1314-21. PubMed ID: 12776285
    [Abstract] [Full Text] [Related]

  • 6. NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children.
    Maruyama K, Iijima K, Ikeda M, Kitamura A, Tsukaguchi H, Yoshiya K, Hoshii S, Wada N, Uemura O, Satomura K, Honda M, Yoshikawa N.
    Pediatr Nephrol; 2003 May 27; 18(5):412-6. PubMed ID: 12687458
    [Abstract] [Full Text] [Related]

  • 7. 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 27; 15(3):722-32. PubMed ID: 14978175
    [Abstract] [Full Text] [Related]

  • 8. 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 27; 13(7):1946-52. PubMed ID: 12089392
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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 28; 22(12):2031-40. PubMed ID: 17899208
    [Abstract] [Full Text] [Related]

  • 11. [Heterozygotic mutation in NPHS2 gene as a cause of familial steroid resistant nephrotic syndrome in two siblings--case report].
    Drozdz D, Pietrzyk JA, Wierzchowska-Słowiaczek E, Sancewicz-Pach K, Antignac C, Miezyński W.
    Przegl Lek; 2006 Dec 28; 63 Suppl 3():85-6. PubMed ID: 16898497
    [Abstract] [Full Text] [Related]

  • 12. First Report of Recurrent Nephrotic Syndrome After Kidney Transplantation in a Patient With NUP93 Gene Mutations: A Case Report.
    Seeman T, Vondrak K.
    Transplant Proc; 2018 Dec 28; 50(10):3954-3956. PubMed ID: 30577294
    [Abstract] [Full Text] [Related]

  • 13. 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 28; 12(12):2742-2746. PubMed ID: 11729243
    [Abstract] [Full Text] [Related]

  • 14. Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
    Dhandapani MC, Venkatesan V, Rengaswamy NB, Gowrishankar K, Ekambaram S, Sengutavan P, Perumal V.
    Clin Exp Nephrol; 2017 Feb 28; 21(1):127-133. PubMed ID: 26820844
    [Abstract] [Full Text] [Related]

  • 15. 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 28; 25(4):854-7. PubMed ID: 24969201
    [Abstract] [Full Text] [Related]

  • 16. 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 28; 13(2):400-405. PubMed ID: 11805168
    [Abstract] [Full Text] [Related]

  • 17. Genetic forms of nephrotic syndrome.
    Niaudet P.
    Pediatr Nephrol; 2004 Dec 28; 19(12):1313-8. PubMed ID: 15503167
    [Abstract] [Full Text] [Related]

  • 18. Successful Preemptive Kidney Transplantation With Rituximab Induction in a Patient With Focal Segmental Glomerulosclerosis and Massive Nephrotic Syndrome: A Case Report.
    Kolonko A, Piecha G, Więcek A.
    Transplant Proc; 2016 Nov 28; 48(9):3092-3094. PubMed ID: 27932154
    [Abstract] [Full Text] [Related]

  • 19. 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 28; 20(3):312-7. PubMed ID: 27312921
    [Abstract] [Full Text] [Related]

  • 20. NPHS2 homozygous p.R229Q variant: potential modifier instead of causal effect in focal segmental glomerulosclerosis.
    Kerti A, Csohány R, Wagner L, Jávorszky E, Maka E, Tory K.
    Pediatr Nephrol; 2013 Oct 28; 28(10):2061-4. PubMed ID: 23800802
    [Abstract] [Full Text] [Related]

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