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

250 related items for PubMed ID: 16874699

  • 1. NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosis.
    Monteiro EJ, Pereira AC, Pereira AB, Krieger JE, Mastroianni-Kirsztajn G.
    J Nephrol; 2006; 19(3):366-71. PubMed ID: 16874699
    [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. [A genetic viewpoint of focal glomerular sclerosis: fom genes to glomerular pathophysiology [corrected]].
    Aucella F, Bisceglia L, Stallone C.
    G Ital Nefrol; 2003 Oct; 20(4):356-67. PubMed ID: 14523896
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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]

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

  • 7. 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]

  • 8. Mutations in NPHS2 in sporadic steroid-resistant nephrotic syndrome in Chinese children.
    Yu Z, Ding J, Huang J, Yao Y, Xiao H, Zhang J, Liu J, Yang J.
    Nephrol Dial Transplant; 2005 May; 20(5):902-8. PubMed ID: 15769810
    [Abstract] [Full Text] [Related]

  • 9. 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; 31(4):273-6. PubMed ID: 23468032
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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]

  • 12. NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele.
    Tsukaguchi H, Sudhakar A, Le TC, Nguyen T, Yao J, Schwimmer JA, Schachter AD, Poch E, Abreu PF, Appel GB, Pereira AB, Kalluri R, Pollak MR.
    J Clin Invest; 2002 Dec; 110(11):1659-66. PubMed ID: 12464671
    [Abstract] [Full Text] [Related]

  • 13. [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; 63 Suppl 3():85-6. PubMed ID: 16898497
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. 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; 12(12):2742-2746. PubMed ID: 11729243
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. 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]

  • 18. 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(11):2062-9. PubMed ID: 24500309
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. 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]

    Page: [Next] [New Search]
    of 13.