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Titlebook: Controversies in Aortic Dissection and Aneurysmal Disease; Robert S. Bonser,Domenico Pagano,Jorge Mascaro Book 2014 Springer-Verlag London

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樓主: 哄笑
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發(fā)表于 2025-3-23 10:45:09 | 只看該作者
12#
發(fā)表于 2025-3-23 15:50:25 | 只看該作者
Value Creation in Leveraged Buyoutss have been operated upon from May 2004 to July 2012, 23 men and 10 women, median age 33 years. All patients are alive and well at the time of last follow-up. Preoperative aortic root diameters were 40–50 mm. All postoperative images were satisfactory with an overall reduction in aortic root dimensi
13#
發(fā)表于 2025-3-23 21:55:27 | 只看該作者
https://doi.org/10.1007/978-3-8350-9352-2toms at presentation, especially in the elderly may be atypical and may include syncope, heart failure, or a lack of pain. Abnormalities on the electrocardiogram, which are common, may lead clinicians to suspect and treat ACS. Additionally, it is not widely recognized that patients with recent aorti
14#
發(fā)表于 2025-3-23 23:54:27 | 只看該作者
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發(fā)表于 2025-3-24 02:21:53 | 只看該作者
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發(fā)表于 2025-3-24 08:34:58 | 只看該作者
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發(fā)表于 2025-3-24 13:02:31 | 只看該作者
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發(fā)表于 2025-3-24 17:36:44 | 只看該作者
Value Creation in European Equity Carve-Outsished and will be summarized here. Furthermore, the aims and rationales of aortic registries are defined. In special sections we describe the methodology of aortic registries, critically discuss possible sources of error and limitations of the approach and we suggest future perspectives for studying
19#
發(fā)表于 2025-3-24 19:54:23 | 只看該作者
The Clinical Genetics of Thoracic Aortic Diseaseon-syndromic conditions have been delineated. These discoveries have led to a better insight into the pathogenesis of aortic aneurysmal disease. Dysregulation of the TGFβ signaling pathway and dysfunction of the contractile apparatus of the smooth muscle cells have emerged as the key players. These
20#
發(fā)表于 2025-3-25 00:31:23 | 只看該作者
When Should Surgery Be Performed in Marfan Syndrome and Other Connective Tissue Disorders to Protect, and another 19 % exhibit a family history of TAAD which is unrelated to Marfan syndrome. Patients with heritable TAAD usually develop aortic rupture or dissection at an age under 40 years. Before the evolution of open-heart surgery, affected persons died from aortic dissection or rupture at young
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