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Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis.
Thromb Res. 2010 Mar;125(3):230-4. doi: 10.1016/j.thromres.2009.05.013. Epub 2009 Jun 17.
Thromb Res. 2010.
PMID: 19535131
The factor V Leiden, prothrombin gene 20210GA, methylenetetrahydrofolate reductase 677CT and platelet glycoprotein IIIa 1565TC mutations in patients with acute ischemic stroke and atrial fibrillation.
Berge E, Haug KB, Sandset EC, Haugbro KK, Turkovic M, Sandset PM.
Berge E, et al. Among authors: haugbro kk.
Stroke. 2007 Mar;38(3):1069-71. doi: 10.1161/01.STR.0000258076.04860.8e. Epub 2007 Feb 8.
Stroke. 2007.
PMID: 17290027
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Anti-dsDNA antibodies and disease classification in antinuclear antibody positive patients: the role of analytical diversity.
Haugbro K, Nossent JC, Winkler T, Figenschau Y, Rekvig OP.
Haugbro K, et al.
Ann Rheum Dis. 2004 Apr;63(4):386-94. doi: 10.1136/ard.2003.016303.
Ann Rheum Dis. 2004.
PMID: 15020332
Free PMC article.
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Alpha-actinin-binding antibodies in relation to systemic lupus erythematosus and lupus nephritis.
Becker-Merok A, Kalaaji M, Haugbro K, Nikolaisen C, Nilsen K, Rekvig OP, Nossent JC.
Becker-Merok A, et al. Among authors: haugbro k.
Arthritis Res Ther. 2006;8(6):R162. doi: 10.1186/ar2070.
Arthritis Res Ther. 2006.
PMID: 17062137
Free PMC article.
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