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Journal Abstract Search

305 related items for PubMed ID: 14523896

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

  • 2. The genetic basis of FSGS and steroid-resistant nephrosis.
    Pollak MR.
    Semin Nephrol; 2003 Mar; 23(2):141-6. PubMed ID: 12704574
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Genetic basis of nephrotic syndrome--review.
    Obeidová H, Merta M, Reiterová J, Maixnerová D, Stekrová J, Rysavá R, Tesar V.
    Prague Med Rep; 2006 Oct; 107(1):5-16. PubMed ID: 16752799
    [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 Oct; 99(2):c31-6. PubMed ID: 15627790
    [Abstract] [Full Text] [Related]

  • 6. 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]

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

  • 8. Mechanisms of disease: focal segmental glomerulosclerosis.
    Meyrier A.
    Nat Clin Pract Nephrol; 2005 Nov; 1(1):44-54. PubMed ID: 16932363
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis.
    Kaplan JM, Kim SH, North KN, Rennke H, Correia LA, Tong HQ, Mathis BJ, Rodríguez-Pérez JC, Allen PG, Beggs AH, Pollak MR.
    Nat Genet; 2000 Mar 15; 24(3):251-6. PubMed ID: 10700177
    [Abstract] [Full Text] [Related]

  • 11. [Structure and function of the glomerular filtration barrier].
    Musiał K, Zwolińska D.
    Pol Merkur Lekarski; 2005 Mar 15; 18(105):317-20. PubMed ID: 15997642
    [Abstract] [Full Text] [Related]

  • 12. Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism.
    Choi HJ, Lee BH, Cho HY, Moon KC, Ha IS, Nagata M, Choi Y, Cheong HI.
    Am J Kidney Dis; 2008 May 15; 51(5):834-8. PubMed ID: 18436095
    [Abstract] [Full Text] [Related]

  • 13. Analysis of mutations in alpha-actinin 4 and podocin genes of patients with chronic renal failure due to sporadic focal segmental glomerulosclerosis.
    Komatsuda A, Wakui H, Maki N, Kigawa A, Goto H, Ohtani H, Hamai K, Oyama Y, Makoto H, Sawada K, Imai H.
    Ren Fail; 2003 Jan 15; 25(1):87-93. PubMed ID: 12617336
    [Abstract] [Full Text] [Related]

  • 14. 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 15; 12(3):341-6. PubMed ID: 18208440
    [Abstract] [Full Text] [Related]

  • 15. 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 15; 24(4):349-54. PubMed ID: 10742096
    [Abstract] [Full Text] [Related]

  • 16. 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 15; 38(10):3486-90. PubMed ID: 17175312
    [Abstract] [Full Text] [Related]

  • 17. 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 15; 10(6):553-6. PubMed ID: 16354237
    [Abstract] [Full Text] [Related]

  • 18. [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 15; 63 Suppl 3():85-6. PubMed ID: 16898497
    [Abstract] [Full Text] [Related]

  • 19. Genetics of focal segmental glomerulosclerosis.
    Woroniecki RP, Kopp JB.
    Pediatr Nephrol; 2007 May 15; 22(5):638-44. PubMed ID: 17347836
    [Abstract] [Full Text] [Related]

  • 20. Familial focal segmental glomerulosclerosis (FSGS) in a Nigerian family and exclusion of mutations in NPHS2,WT1 and APOL1.
    Anochie IC, Eke FU, Okpere AN.
    West Afr J Med; 2012 May 15; 31(4):273-6. PubMed ID: 23468032
    [Abstract] [Full Text] [Related]

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