描述 发表于 2025-3-23 10:45:09
http://reply.papertrans.cn/24/2377/237669/237669_11.png毛细血管 发表于 2025-3-23 15:50:25
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 dimensicarotid-bruit 发表于 2025-3-23 21:55:27
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 aortiintention 发表于 2025-3-23 23:54:27
http://reply.papertrans.cn/24/2377/237669/237669_14.png包庇 发表于 2025-3-24 02:21:53
http://reply.papertrans.cn/24/2377/237669/237669_15.png裙带关系 发表于 2025-3-24 08:34:58
http://reply.papertrans.cn/24/2377/237669/237669_16.pngLumbar-Spine 发表于 2025-3-24 13:02:31
http://reply.papertrans.cn/24/2377/237669/237669_17.pngJacket 发表于 2025-3-24 17:36:44
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 studyingHay-Fever 发表于 2025-3-24 19:54:23
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. Thesedefuse 发表于 2025-3-25 00:31:23
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