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

159 related items for PubMed ID: 17699384

  • 1. Recessive NPHS2 (Podocin) mutations are rare in adult-onset idiopathic focal segmental glomerulosclerosis.
    He N, Zahirieh A, Mei Y, Lee B, Senthilnathan S, Wong B, Mucha B, Hildebrandt F, Cole DE, Cattran D, Pei Y.
    Clin J Am Soc Nephrol; 2007 Jan; 2(1):31-7. PubMed ID: 17699384
    [Abstract] [Full Text] [Related]

  • 2. NPHS2 variation in focal and segmental glomerulosclerosis.
    Tonna SJ, Needham A, Polu K, Uscinski A, Appel GB, Falk RJ, Katz A, Al-Waheeb S, Kaplan BS, Jerums G, Savige J, Harmon J, Zhang K, Curhan GC, Pollak MR.
    BMC Nephrol; 2008 Sep 29; 9():13. PubMed ID: 18823551
    [Abstract] [Full Text] [Related]

  • 3. 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 29; 110(11):1659-66. PubMed ID: 12464671
    [Abstract] [Full Text] [Related]

  • 4. 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 29; 6(2):344-54. PubMed ID: 20947785
    [Abstract] [Full Text] [Related]

  • 5. 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; 29(11):2062-9. PubMed ID: 24500309
    [Abstract] [Full Text] [Related]

  • 6. Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa.
    Nandlal L, Winkler CA, Bhimma R, Cho S, Nelson GW, Haripershad S, Naicker T.
    Eur J Pediatr; 2022 Oct 29; 181(10):3595-3606. PubMed ID: 35920919
    [Abstract] [Full Text] [Related]

  • 7. Prevalence of the NPHS2 variants p.R229Q, p.A242V, and p.R138Q in patients with focal segmental glomerulosclerosis.
    de Almeida R, da Silva WC, Garbin HI, Itaquy TP, Dos Santos Pereira F, Garcia CD, Keitel E, Sales Luiz Vianna F, Veronese FV.
    Clin Nephrol; 2020 Oct 29; 94(4):187-196. PubMed ID: 32691731
    [Abstract] [Full Text] [Related]

  • 8. 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 29; 12(12):2742-2746. PubMed ID: 11729243
    [Abstract] [Full Text] [Related]

  • 9. The p.R229Q variant of the NPHS2 (podocin) gene in focal segmental glomerulosclerosis and steroid-resistant nephrotic syndrome: a meta-analysis.
    Lu L, Wan H, Yin Y, Feng WJ, Wang M, Zou YC, Huang B, Wang DT, Shi Y, Zhao Y, Wei LB.
    Int Urol Nephrol; 2014 Jul 29; 46(7):1383-93. PubMed ID: 24715228
    [Abstract] [Full Text] [Related]

  • 10. 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 29; 21(1):127-133. PubMed ID: 26820844
    [Abstract] [Full Text] [Related]

  • 11. Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.
    Bińczak-Kuleta A, Rubik J, Litwin M, Ryder M, Lewandowska K, Taryma-Leśniak O, Clark JS, Grenda R, Ciechanowicz A.
    Bosn J Basic Med Sci; 2014 May 29; 14(2):89-93. PubMed ID: 24856380
    [Abstract] [Full Text] [Related]

  • 12. 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 29; 12(3):341-6. PubMed ID: 18208440
    [Abstract] [Full Text] [Related]

  • 13. 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 29; 28(10):2061-4. PubMed ID: 23800802
    [Abstract] [Full Text] [Related]

  • 14. NPHS2 variation in sporadic focal segmental glomerulosclerosis.
    McKenzie LM, Hendrickson SL, Briggs WA, Dart RA, Korbet SM, Mokrzycki MH, Kimmel PL, Ahuja TS, Berns JS, Simon EE, Smith MC, Trachtman H, Michel DM, Schelling JR, Cho M, Zhou YC, Binns-Roemer E, Kirk GD, Kopp JB, Winkler CA.
    J Am Soc Nephrol; 2007 Nov 29; 18(11):2987-95. PubMed ID: 17942957
    [Abstract] [Full Text] [Related]

  • 15. Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.
    Reiterová J, Safránková H, Obeidová L, Stěkrová J, Maixnerová D, Merta M, Tesař V.
    Folia Biol (Praha); 2012 Nov 29; 58(2):64-8. PubMed ID: 22578956
    [Abstract] [Full Text] [Related]

  • 16. 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 29; 41(6):1314-21. PubMed ID: 12776285
    [Abstract] [Full Text] [Related]

  • 17. NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosis.
    Monteiro EJ, Pereira AC, Pereira AB, Krieger JE, Mastroianni-Kirsztajn G.
    J Nephrol; 2006 Jun 29; 19(3):366-71. PubMed ID: 16874699
    [Abstract] [Full Text] [Related]

  • 18. 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 Jun 29; 31(4):273-6. PubMed ID: 23468032
    [Abstract] [Full Text] [Related]

  • 19. 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 29; 23(10):3146-51. PubMed ID: 18443213
    [Abstract] [Full Text] [Related]

  • 20. 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 29; 99(2):c31-6. PubMed ID: 15627790
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.