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Journal Abstract Search

121 related items for PubMed ID: 16410540

  • 1. Lack of association of mannose binding lectin variant alleles with systemic lupus erythematosus.
    Momot T, Ahmadi-Simab K, Gause A, Gross WL, Gromnica-Ihle E, Peter HH, Manger K, Zeidler H, Schmidt RE, Witte T.
    Ann Rheum Dis; 2006 Feb; 65(2):278-9. PubMed ID: 16410540
    [No Abstract] [Full Text] [Related]

  • 2. Mannose-binding lectin variant alleles and the risk of arterial thrombosis in systemic lupus erythematosus.
    Øhlenschlaeger T, Garred P, Madsen HO, Jacobsen S.
    N Engl J Med; 2004 Jul 15; 351(3):260-7. PubMed ID: 15254284
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  • 5. Genetically determined serum levels of mannose-binding lectin correlate negatively with common carotid intima-media thickness in systemic lupus erythematosus.
    Troelsen LN, Garred P, Christiansen B, Torp-Pedersen C, Jacobsen S.
    J Rheumatol; 2010 Sep 15; 37(9):1815-21. PubMed ID: 20595266
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  • 6. MBL2 gene variants coding for mannose-binding lectin deficiency are associated with increased risk of nephritis in Danish patients with systemic lupus erythematosus.
    Tanha N, Troelsen L, From Hermansen ML, Kjær L, Faurschou M, Garred P, Jacobsen S.
    Lupus; 2014 Oct 15; 23(11):1105-11. PubMed ID: 24850777
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  • 7. Arterial thrombosis in systemic lupus erythematosus.
    Tanvetyanon T.
    N Engl J Med; 2004 Oct 28; 351(18):1910-1; author reply 1910-1. PubMed ID: 15515221
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  • 8. Mannose-binding lectin is a disease-modifying factor in North American patients with systemic lupus erythematosus.
    Piao W, Liu CC, Kao AH, Manzi S, Vogt MT, Ruffing MJ, Ahearn JM.
    J Rheumatol; 2007 Jul 28; 34(7):1506-13. PubMed ID: 17610319
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  • 9. Genetically determined mannan-binding lectin deficiency is of minor importance in determining susceptibility to severe infections and vascular organ damage in systemic lupus erythematosus.
    Jönsen A, Gullstrand B, Güner N, Bengtsson AA, Nived O, Truedsson L, Sturfelt G.
    Lupus; 2007 Jul 28; 16(4):245-53. PubMed ID: 17439930
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  • 10. Systemic lupus erythematosus in a multiethnic US cohort: XXXIV. Deficient mannose-binding lectin exon 1 polymorphisms are associated with cerebrovascular but not with other arterial thrombotic events.
    Calvo-Alén J, Alarcón GS, Tew MB, Tan FK, McGwin G, Fessler BJ, Vilá LM, Reveille JD, LUMINA Study Group.
    Arthritis Rheum; 2006 Jun 28; 54(6):1940-5. PubMed ID: 16729310
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  • 12. Mannose-binding lectin and susceptibility to infection in Chinese patients with systemic lupus erythematosus.
    Mok MY, Ip WK, Lau CS, Lo Y, Wong WH, Lau YL.
    J Rheumatol; 2007 Jun 28; 34(6):1270-6. PubMed ID: 17552055
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  • 13. Association of three systemic lupus erythematosus susceptibility factors, PD-1.3A, C4AQ0, and low levels of mannan-binding lectin, with autoimmune manifestations in Icelandic multicase systemic lupus erythematosus families.
    Kristjansdottir H, Saevarsdottir S, Gröndal G, Alarcón-Riquelme ME, Erlendsson K, Valdimarsson H, Steinsson K.
    Arthritis Rheum; 2008 Dec 28; 58(12):3865-72. PubMed ID: 19035512
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  • 16. [The role of mannose binding lectin in the pathogenesis of systemic lupus erythematosus].
    Li SG, Huang F, Liu XY, Deng XX, Xu M, Cong XZ, Ding YZ, Guo JH, Deng XH, Zhao MS.
    Zhonghua Yi Xue Za Zhi; 2006 Feb 21; 86(7):463-7. PubMed ID: 16677572
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  • 19. Low clinical penetrance of mannose-binding lectin-associated serine protease 2 deficiency.
    García-Laorden MI, García-Saavedra A, de Castro FR, Violán JS, Rajas O, Blanquer J, Borderías L, Rodríguez-Gallego C.
    J Allergy Clin Immunol; 2006 Dec 21; 118(6):1383-6. PubMed ID: 17137870
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  • 20. Variant mannose-binding lectin 2 genotype is a risk factor for reactive systemic amyloidosis in rheumatoid arthritis.
    Maury CP, Aittoniemi J, Tiitinen S, Laiho K, Kaarela K, Hurme M.
    J Intern Med; 2007 Oct 21; 262(4):466-9. PubMed ID: 17875183
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