Peripartum management of hereditary thrombophilia: results of primary surveillance in Japan
Author:
Funder
Ministry of Health, Labour and Welfare
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
https://link.springer.com/content/pdf/10.1007/s12185-022-03354-4.pdf
Reference30 articles.
1. Kobayashi T, Morishita E, Tsuda H, Neki R, Kojima T, Ohga S, et al. Clinical guidance for peripartum management of patients with hereditary thrombophilia. J Obstet Gynecol Res. 2021;47:3008–33.
2. Tang W, Teichert M, Chasman DI, Heit JA, Morange PE, Li G, et al. A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. Genet Epidemiol. 2013;37:512–21.
3. Seligsohn U, Lubestsky A. Genetic susceptibility to venous thrombosis. N Engl J Med. 2001;344:1222–31.
4. Caspers M, Pavlova A, Driesen J, Harbrecht U, Klamroth R, Kadar J, et al. Deficiencies of antithrombin, protein C and protein S - practical experience in genetic analysis of a large patient cohort. Thromb Haemost. 2012;108:247–57.
5. Middeldorp S, van Hylckama VA. Does thrombophilia testing help in the clinical management of patients? Br J Haematol. 2008;143:321–35.
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