两名无症状遗传性异常纤维蛋白原血症患者的外科治疗 - Suppr

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[Surgical treatment of two patients with asymptomatic hereditary abnormal fibrinogen].

作者信息

Luo M L, Yan J, Lin F Q, Cheng P, Deng D H

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2017 Sep 14;38(9):797-798. doi: 10.3760/cma.j.issn.0253-2727.2017.09.013.

DOI:10.3760/cma.j.issn.0253-2727.2017.09.013

PMID:29081199

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7348365/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbd9/7348365/975fe938af9a/cjh-38-09-797-g001.jpg

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本文引用的文献

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Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His.

Medicine (Baltimore). 2016 Sep;95(39):e4864. doi: 10.1097/MD.0000000000004864.

Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders.

Semin Thromb Hemost. 2016 Jun;42(4):356-65. doi: 10.1055/s-0036-1571340. Epub 2016 Mar 28.

Clinical Features and Management of Congenital Fibrinogen Deficiencies.

Semin Thromb Hemost. 2016 Jun;42(4):366-74. doi: 10.1055/s-0036-1571339. Epub 2016 Mar 28.

Dysfibrinogenemia in a patient undergoing artificial abortion after misdiagnosis and review of the literature.

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J Thromb Haemost. 2015 Jun;13(6):909-19. doi: 10.1111/jth.12916. Epub 2015 May 2.

Natural history of patients with congenital dysfibrinogenemia.

Blood. 2015 Jan 15;125(3):553-61. doi: 10.1182/blood-2014-06-582866. Epub 2014 Oct 15.

Guideline for the diagnosis and management of the rare coagulation disorders: a United Kingdom Haemophilia Centre Doctors' Organization guideline on behalf of the British Committee for Standards in Haematology.

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