[Consensus of Chinese expert on the diagnosis and treatment of rare bleeding disorders (version 2021)].
出版信息
Zhonghua Xue Ye Xue Za Zhi. 2021 Feb 14;42(2):89-96. doi: 10.3760/cma.j.issn.0253-2727.2021.02.001.
Abstract
摘要
相似文献
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[Consensus of Chinese expert on the diagnosis and treatment of rare bleeding disorders (version 2021)].《中国罕见出血性疾病诊断与治疗专家共识（2021年版）》
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本文引用的文献
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The World Federation of Hemophilia Annual Global Survey 1999-2018.《世界血友病联盟 1999-2018 年全球年度调查》。
Haemophilia. 2020 Jul;26(4):591-600. doi: 10.1111/hae.14012. Epub 2020 Jun 4.
2
Women and inherited bleeding disorders - A review with a focus on key challenges for 2019.女性与遗传性出血性疾病——2019年重点挑战综述
Transfus Apher Sci. 2019 Oct;58(5):613-622. doi: 10.1016/j.transci.2019.08.013. Epub 2019 Aug 9.
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Low factor V level ameliorates bleeding diathesis in patients with combined deficiency of factor V and factor VIII.低因子 V 水平可改善因子 V 和因子 VIII 联合缺乏症患者的出血倾向。
Blood. 2019 Nov 14;134(20):1745-1754. doi: 10.1182/blood.2018886069.
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Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.对 2396 名出血、血栓形成和血小板疾病患者进行诊断性高通量测序。
Blood. 2019 Dec 5;134(23):2082-2091. doi: 10.1182/blood.2018891192.
5
Molecular Diagnosis of Inherited Coagulation and Bleeding Disorders.遗传性凝血和出血性疾病的分子诊断。
Semin Thromb Hemost. 2019 Oct;45(7):695-707. doi: 10.1055/s-0039-1687889. Epub 2019 Apr 30.
6
Treatment of rare factor deficiencies other than hemophilia.除血友病以外的其他罕见因子缺乏症的治疗。
Blood. 2019 Jan 31;133(5):415-424. doi: 10.1182/blood-2018-06-820738. Epub 2018 Dec 17.
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Phenotypical variability in congenital FVII deficiency follows the ISTH-SSC severity classification guidelines: a review with illustrative examples from the clinic.先天性FVII缺乏症的表型变异性遵循ISTH-SSC严重程度分类指南：附临床实例的综述
J Blood Med. 2018 Nov 19;9:211-218. doi: 10.2147/JBM.S157633. eCollection 2018.
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Rare congenital bleeding disorders.罕见的先天性出血性疾病。
Ann Transl Med. 2018 Sep;6(17):331. doi: 10.21037/atm.2018.08.34.
9
Inhibitors in Patients with Congenital Bleeding Disorders Other Than Hemophilia.除血友病以外的先天性出血性疾病患者的抑制剂。
Semin Thromb Hemost. 2018 Sep;44(6):595-603. doi: 10.1055/s-0037-1607441. Epub 2017 Nov 17.
10
Paradoxical bleeding and thrombotic episodes of dysprothrombinaemia due to a homozygous Arg382His mutation.由于纯合子Arg382His突变导致的凝血异常血症的矛盾性出血和血栓形成事件。
Thromb Haemost. 2017 Feb 28;117(3):479-490. doi: 10.1160/TH16-10-0750. Epub 2016 Dec 15.
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