2014
DOI: 10.1016/j.autrev.2014.07.004
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Hypercoagulability in celiac disease — An update

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Cited by 36 publications
(29 citation statements)
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“…Other possible explanations include genetic predisposition methylenetetrahydrofolate reductase (MTHFR mutations), platelet abnormality, and autoimmune homology between tissue transgluminase and factor XIII …”
Section: Discussionmentioning
confidence: 84%
See 1 more Smart Citation
“…Other possible explanations include genetic predisposition methylenetetrahydrofolate reductase (MTHFR mutations), platelet abnormality, and autoimmune homology between tissue transgluminase and factor XIII …”
Section: Discussionmentioning
confidence: 84%
“…Other possible explanations include genetic predisposition methylenetetrahydrofolate reductase (MTHFR mutations), platelet abnormality, and autoimmune homology between tissue transgluminase and factor XIII. 30 Even though the primary studies included in this meta-analysis were of high quality as reflected by the high-quality assessment scores, we acknowledged that there were some limitations. Thus, the results of our study should be interpreted with caution.…”
Section: Discussionmentioning
confidence: 99%
“…To our knowledge, this is the first report of a multiple arterial thrombotic case associated with a CD. The cause of the vascular disorders seen in patients with CD remains controversial [9]. The presence of thrombophilic risk factors for thrombosis, such as protein S deficiency, hyperhomocysteinemia, or antiphospholipid antibodies, was reported depending on the case, although, our patient had none of these thrombophilic factors.…”
Section: Figurementioning
confidence: 66%
“…A wind of change that is blowing in the management of celiac disease. Lerner and Blank [23] remarkably displayed the concomitant association between hypercoagulable autoimmune diseases and celiac. The presence of SLE and/or antiphospholipid antibodies and of other prothrombotic states such as nutritional deficiencies of B12 and folate, protein C and S deficiencies due to vitamin K deficiency, genetic thrombophilia, accelerated atherosclerosis with endothelial dysfunction and finally, platelet abnormalities may combine to bring about a condition of hypercoagulability.…”
Section: Contents Lists Available At Sciencedirectmentioning
confidence: 98%