These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

378 related items for PubMed ID: 12704574

  • 1. 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]

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

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

  • 4. 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]

  • 5. Molecular basis of steroid-resistant nephrotic syndrome.
    Antignac C.
    Nefrologia; 2005 Oct; 25 Suppl 2():25-8. PubMed ID: 16050398
    [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. [Structure and function of the glomerular filtration barrier].
    Musiał K, Zwolińska D.
    Pol Merkur Lekarski; 2005 Mar; 18(105):317-20. PubMed ID: 15997642
    [Abstract] [Full Text] [Related]

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

  • 9. TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.
    Gigante M, Caridi G, Montemurno E, Soccio M, d'Apolito M, Cerullo G, Aucella F, Schirinzi A, Emma F, Massella L, Messina G, De Palo T, Ranieri E, Ghiggeri GM, Gesualdo L.
    Clin J Am Soc Nephrol; 2011 Jul; 6(7):1626-34. PubMed ID: 21734084
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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; 47(7):445-52. PubMed ID: 20591883
    [Abstract] [Full Text] [Related]

  • 12. 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 Jul; 99(2):c31-6. PubMed ID: 15627790
    [Abstract] [Full Text] [Related]

  • 13. [Characterization of the NPH2 gene, coding for the glomerular protein podocin, implicated in a familial form of cortico-resistant nephrotic syndrome transmitted as an autosomal recessive].
    Boute N, Roselli S, Gribouval O, Niaudet P, Gubler MC, Antignac C.
    Nephrologie; 2002 Jul; 23(1):35-6. PubMed ID: 11908478
    [No Abstract] [Full Text] [Related]

  • 14. NPHS2 mutations in children with steroid-resistant nephrotic syndrome.
    Otukesh H, Ghazanfari B, Fereshtehnejad SM, Bakhshayesh M, Hashemi M, Hoseini R, Chalian M, Salami A, Mehdipor L, Rahiminia A.
    Iran J Kidney Dis; 2009 Apr; 3(2):99-102. PubMed ID: 19395786
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. [Focal segmental glomerulosclerosis].
    Yuzawa Y, Matsuo S.
    Nihon Rinsho; 2004 Oct; 62(10):1837-41. PubMed ID: 15500127
    [Abstract] [Full Text] [Related]

  • 17. Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome.
    Santín S, Tazón-Vega B, Silva I, Cobo MÁ, Giménez I, Ruíz P, García-Maset R, Ballarín J, Torra R, Ars E, FSGS Spanish Study Group.
    Clin J Am Soc Nephrol; 2011 Feb; 6(2):344-54. PubMed ID: 20947785
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. [Therapeutic apheresis in idiopathic nephrotic syndrome].
    Moriconi L.
    G Ital Nefrol; 2012 Feb 15; 29 Suppl 54():S67-72. PubMed ID: 22388834
    [Abstract] [Full Text] [Related]

  • 20. Molecular pathology of nephrotic syndrome in childhood: a contemporary approach to diagnosis.
    Liapis H.
    Pediatr Dev Pathol; 2008 Feb 15; 11(4):154-63. PubMed ID: 18462046
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 19.