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Journal Abstract Search

130 related items for PubMed ID: 11793129

  • 1. Another autosomal recessive form of focal glomerulosclerosis with neurological findings.
    Nakazato H, Hattori S, Karashima S, Kawano T, Seguchi S, Kanahori M, Endo F.
    Pediatr Nephrol; 2002 Jan; 17(1):16-9. PubMed ID: 11793129
    [Abstract] [Full Text] [Related]

  • 2. Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis.
    Löwik M, Levtchenko E, Westra D, Groenen P, Steenbergen E, Weening J, Lilien M, Monnens L, van den Heuvel L.
    Nephrol Dial Transplant; 2008 Oct; 23(10):3146-51. PubMed ID: 18443213
    [Abstract] [Full Text] [Related]

  • 3. Collapsing glomerulopathy in Galloway-Mowat syndrome: a case report and review of the literature.
    Sartelet H, Pietrement C, Noel LH, Sabouraud P, Birembaut P, Oligny LL, Roussel B, Doco-Fenzy M.
    Pathol Res Pract; 2008 Oct; 204(6):401-6. PubMed ID: 18276083
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  • 4. Late-onset nephrotic syndrome and severe cerebellar atrophy in Galloway-Mowat syndrome.
    Steiss JO, Gross S, Neubauer BA, Hahn A.
    Neuropediatrics; 2005 Oct; 36(5):332-5. PubMed ID: 16217710
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  • 5. NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosis.
    Monteiro EJ, Pereira AC, Pereira AB, Krieger JE, Mastroianni-Kirsztajn G.
    J Nephrol; 2006 Oct; 19(3):366-71. PubMed ID: 16874699
    [Abstract] [Full Text] [Related]

  • 6. Microcephaly, focal segmental glomerulonephritis and marfanoid habitus in two sibs.
    Houlston RS, Iraggori S, Murday V, Scrine M, Macdermot K, Slack J, Rees L.
    Clin Dysmorphol; 1992 Apr; 1(2):111-3. PubMed ID: 1345513
    [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; 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; 44(2):e22-24. PubMed ID: 15264208
    [Abstract] [Full Text] [Related]

  • 9. Late onset of familial nephrotic syndrome associated with a compound heterozygous mutation of the podocin-encoding gene.
    Ardiles LG, Carrasco AE, Carpio JD, Mezzano SA.
    Nephrology (Carlton); 2005 Dec; 10(6):553-6. PubMed ID: 16354237
    [Abstract] [Full Text] [Related]

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

  • 11. Novel mutations in NPHP4 in a consanguineous family with histological findings of focal segmental glomerulosclerosis.
    Mistry K, Ireland JH, Ng RC, Henderson JM, Pollak MR.
    Am J Kidney Dis; 2007 Nov; 50(5):855-64. PubMed ID: 17954299
    [Abstract] [Full Text] [Related]

  • 12. 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; 107(1):5-16. PubMed ID: 16752799
    [Abstract] [Full Text] [Related]

  • 13. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome.
    Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler MC, Niaudet P, Antignac C.
    Nat Genet; 2000 Apr; 24(4):349-54. PubMed ID: 10742096
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  • 15. 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 Apr; 99(2):c31-6. PubMed ID: 15627790
    [Abstract] [Full Text] [Related]

  • 16. Focal segmental glomerulosclerosis and renal transplantation.
    Crosson JT.
    Transplant Proc; 2007 Apr; 39(3):737-43. PubMed ID: 17445586
    [Abstract] [Full Text] [Related]

  • 17. CD80, suPAR and nephrotic syndrome in a case of NPHS2 mutation.
    Cara-Fuentes G, Araya C, Wei C, Rivard C, Ishimoto T, Reiser J, Johnson RJ, Garin EH.
    Nefrologia; 2013 Apr; 33(5):727-31. PubMed ID: 24089165
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  • 20. [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 Apr; 63 Suppl 3():85-6. PubMed ID: 16898497
    [Abstract] [Full Text] [Related]

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