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在一个大型跨国遗传性出血性毛细血管扩张症患者登记处中,对肺动静脉畸形的表现、并发症及治疗方面的性别差异进行分析。

An analysis of sex differences in pulmonary arteriovenous malformation presentation, complications and management in a large, multinational registry of patients with hereditary haemorrhagic telangiectasia.

作者信息

Tuff-Gordon Eliza, Faughnan Marie E, Kim Helen, Lawton Michael T, Vozoris Nicholas T

机构信息

University of Ottawa, Ottawa, ON, Canada.

Toronto HHT Centre, Keenan Research Centre in the Li Ka Shing Knowledge Institute, St Michael's Hospital, Toronto, ON, Canada.

出版信息

ERJ Open Res. 2023 May 22;9(3). doi: 10.1183/23120541.00751-2022. eCollection 2023 May.

摘要

https://bit.ly/3TNLA6v. (链接无法直接翻译,保留原文)

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本文引用的文献

1
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Ann Am Thorac Soc. 2022 Aug;19(8):1432-1435. doi: 10.1513/AnnalsATS.202202-130RL.
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Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia.
Ann Intern Med. 2020 Dec 15;173(12):989-1001. doi: 10.7326/M20-1443. Epub 2020 Sep 8.
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Curr Opin Pulm Med. 2014 Sep;20(5):421-8. doi: 10.1097/MCP.0000000000000076.
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J Med Genet. 2011 Feb;48(2):73-87. doi: 10.1136/jmg.2009.069013. Epub 2009 Jun 23.
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The pulmonary vascular complications of hereditary haemorrhagic telangiectasia.
Eur Respir J. 2009 May;33(5):1186-94. doi: 10.1183/09031936.00061308.
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Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).
Am J Med Genet. 2000 Mar 6;91(1):66-7. doi: 10.1002/(sici)1096-8628(20000306)91:1<66::aid-ajmg12>3.0.co;2-p.

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