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of Aortic Dissection Caused by Hypertension and Marfan Syndrome的研究。该研究中,研究人员共收集了11个主动脉样本进行单细胞RNA测序及分析(吉凯基因提供),揭示了20个集群,包括
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Hu, Yufei Wu, Yangkai Xu, Hongtu Cui, Hong S Lu, *Lemin Zheng. The mechanism and therapy of aortic aneurysms. Signal
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thrombosis,DVT)形成的重要依据。2、D-二聚体与急性主动脉夹层的诊断Weber为一例因胸痛和D-二聚体升高而怀疑PE的患者行心脏彩超检查以评估肺动脉压时,意外发现此患者诊断并非PE,而是主动脉夹层(aortic
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target in aortic aneurysm and dissection)”为题,2021年9月18日在线发表于《欧洲心脏杂志》(European Heart Journal),论文链接:https://academic.oup.com
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先天性主动脉-左心室隧道(aortic-left ventrieular
tunnel,ALVT)相鉴别。ALVT是一种罕见的先天性心脏畸形,其发病率仅占先天性心脏病的0.12%,系指主动脉与左心室间存在位于主动脉瓣膜旁侧的异常通道。 该
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in this gene have been associated with Marfan Syndrome, Loeys-Deitz Aortic Aneurysm Syndrome, and the development
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(Transcatheter Aortic Valve Implantation,TAVI)。 手术过程:患者入室后行常规监测及脑电双频指数(Bispectral index,BIS)监测,安置体外除颤电极,放置呼末监测管及面罩给氧。局麻下行桡动脉穿刺置管
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, for pulsatile flows, in particular for aortic blood flow, turbulence levels remain low despite relatively large peak
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, and tumorigenesis. Mutations in this gene have been associated with Marfan Syndrome, Loeys-Deitz Aortic Aneurysm Syndrome
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腔完全消失。 3月后CTA复查支架无移位,见图4,仿真内镜显示支架内通畅。 2讨论 主动脉夹层(Aortic Dissection,AD)是动脉壁存在或不存在自身病变的基础上,在一系列的可能的外因作用下,使动脉壁内层破裂,血液通过破裂的动脉