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Journal Abstract Search

378 related items for PubMed ID: 24161036

  • 1. Dense deposit disease and C3 glomerulopathy.
    Barbour TD, Pickering MC, Terence Cook H.
    Semin Nephrol; 2013 Nov; 33(6):493-507. PubMed ID: 24161036
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  • 4. Alternative pathway dysfunction in kidney disease: a case report and review of dense deposit disease and C3 glomerulopathy.
    Hawfield A, Iskandar SS, Smith RJ.
    Am J Kidney Dis; 2013 May; 61(5):828-31. PubMed ID: 23391537
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  • 5. Retinal disease in the C3 glomerulopathies and the risk of impaired vision.
    Savige J, Amos L, Ierino F, Mack HG, Symons RC, Hughes P, Nicholls K, Colville D.
    Ophthalmic Genet; 2016 Dec; 37(4):369-376. PubMed ID: 26915021
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  • 6. von Willebrand factor variants in C3 glomerulopathy: A Chinese cohort study.
    Chen YY, Han SS, Cao Y, Yu XJ, Zhu L, Luo JC, Song WC, Yu F, Mao YH, Zhao MH.
    Clin Immunol; 2021 Aug; 229():108794. PubMed ID: 34245915
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  • 7. Update on C3 glomerulopathy.
    Barbour TD, Ruseva MM, Pickering MC.
    Nephrol Dial Transplant; 2016 May; 31(5):717-25. PubMed ID: 25326473
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  • 9. Combination of factor H mutation and properdin deficiency causes severe C3 glomerulonephritis.
    Lesher AM, Zhou L, Kimura Y, Sato S, Gullipalli D, Herbert AP, Barlow PN, Eberhardt HU, Skerka C, Zipfel PF, Hamano T, Miwa T, Tung KS, Song WC.
    J Am Soc Nephrol; 2013 Jan; 24(1):53-65. PubMed ID: 23204401
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  • 10. C3 glomerulonephritis and dense deposit disease share a similar disease course in a large United States cohort of patients with C3 glomerulopathy.
    Bomback AS, Santoriello D, Avasare RS, Regunathan-Shenk R, Canetta PA, Ahn W, Radhakrishnan J, Marasa M, Rosenstiel PE, Herlitz LC, Markowitz GS, D'Agati VD, Appel GB.
    Kidney Int; 2018 Apr; 93(4):977-985. PubMed ID: 29310824
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  • 12. A novel CFHR1-CFHR5 hybrid leads to a familial dominant C3 glomerulopathy.
    Togarsimalemath SK, Sethi SK, Duggal R, Le Quintrec M, Jha P, Daniel R, Gonnet F, Bansal S, Roumenina LT, Fremeaux-Bacchi V, Kher V, Dragon-Durey MA.
    Kidney Int; 2017 Oct; 92(4):876-887. PubMed ID: 28729035
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  • 13. C3 glomerulopathy: the genetic and clinical findings in dense deposit disease and C3 glomerulonephritis.
    Xiao X, Pickering MC, Smith RJ.
    Semin Thromb Hemost; 2014 Jun; 40(4):465-71. PubMed ID: 24799308
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  • 14. Recent insights into C3 glomerulopathy.
    Barbour TD, Pickering MC, Cook HT.
    Nephrol Dial Transplant; 2013 Jul; 28(7):1685-93. PubMed ID: 23479095
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  • 15. Redefining C3 glomerulopathy: 'C3 only' is a bridge too far.
    Larsen CP, Walker PD.
    Kidney Int; 2013 Feb; 83(2):331-2. PubMed ID: 23364589
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  • 18. C3 Glomerulopathy: Pathogenesis and Treatment.
    Ahmad SB, Bomback AS.
    Adv Chronic Kidney Dis; 2020 Mar; 27(2):104-110. PubMed ID: 32553242
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  • 20. Loss of properdin exacerbates C3 glomerulopathy resulting from factor H deficiency.
    Ruseva MM, Vernon KA, Lesher AM, Schwaeble WJ, Ali YM, Botto M, Cook T, Song W, Stover CM, Pickering MC.
    J Am Soc Nephrol; 2013 Jan; 24(1):43-52. PubMed ID: 23184055
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