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

282 related items for PubMed ID: 24969201

  • 61. 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]

  • 62. Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin.
    Caridi G, Berdeli A, Dagnino M, Di Duca M, Mir S, Cura A, Ravazzolo R, Ghiggeri GM.
    Am J Kidney Dis; 2004 Apr; 43(4):727-32. PubMed ID: 15042551
    [Abstract] [Full Text] [Related]

  • 63. A partial response to abatacept in a patient with steroid resistant focal segmental glomerulosclerosis.
    Soyaltın E, Demir BK, Alparslan C, Çamlar SA, Alaygut D, Yavaşcan Ö, Mutlubaş F.
    Turk J Pediatr; 2020 Apr; 62(4):663-667. PubMed ID: 32779421
    [Abstract] [Full Text] [Related]

  • 64. [Mutations in NPHS2 in familial steroid-resistant nephrotic syndrome in Southern Chinese Han ethnic group].
    Fu R, Chen XM, Wang QH, Chen SP, Yu ZH, Ye LY, Ren RN, Huang J, Wang CF.
    Zhonghua Er Ke Za Zhi; 2008 Aug; 46(8):591-6. PubMed ID: 19099831
    [Abstract] [Full Text] [Related]

  • 65.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 66. Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome.
    Büscher AK, Kranz B, Büscher R, Hildebrandt F, Dworniczak B, Pennekamp P, Kuwertz-Bröking E, Wingen AM, John U, Kemper M, Monnens L, Hoyer PF, Weber S, Konrad M.
    Clin J Am Soc Nephrol; 2010 Nov; 5(11):2075-84. PubMed ID: 20798252
    [Abstract] [Full Text] [Related]

  • 67.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 68. WT1 and NPHS2 mutations in Korean children with steroid-resistant nephrotic syndrome.
    Cho HY, Lee JH, Choi HJ, Lee BH, Ha IS, Choi Y, Cheong HI.
    Pediatr Nephrol; 2008 Jan; 23(1):63-70. PubMed ID: 17934764
    [Abstract] [Full Text] [Related]

  • 69. NPHS2 R229Q polymorphism in steroid resistant nephrotic syndrome: is it responsive to immunosuppressive therapy?
    Mishra OP, Kakani N, Singh AK, Narayan G, Abhinay A, Prasad R, Batra VV.
    J Trop Pediatr; 2014 Jun; 60(3):231-7. PubMed ID: 24519673
    [Abstract] [Full Text] [Related]

  • 70. Characterization of NPHS2 gene polymorphisms associated to steroid resistance nephrotic syndrome in Indian children.
    Joshi BB, Mistry KN, Gang S, Koringa PG, Joshi CG.
    Gene; 2017 Sep 10; 628():134-140. PubMed ID: 28712774
    [Abstract] [Full Text] [Related]

  • 71.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 72.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 73. 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 10; 6(7):1626-34. PubMed ID: 21734084
    [Abstract] [Full Text] [Related]

  • 74.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 75.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 76.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 77. Plasmapheresis-induced clinical improvement in a patient with steroid-resistant nephrotic syndrome due to podocin (NPHS2) gene mutation.
    Skálová S, Podhola M, Vondrák K, Chernin G.
    Acta Medica (Hradec Kralove); 2010 Jul 10; 53(3):157-9. PubMed ID: 21171529
    [Abstract] [Full Text] [Related]

  • 78.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 79. 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 10; 110(11):1659-66. PubMed ID: 12464671
    [Abstract] [Full Text] [Related]

  • 80.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 15.