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Titlebook: Cardiovascular Aspects of Marfan Syndrome; R. Hetzer,P. Gehle,J. Ennker Book 1995 Dr. Dietrich Steinkopff Verlag GmbH & Co. KG, Darmstadt

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樓主: 淺吟低唱
31#
發(fā)表于 2025-3-26 22:43:07 | 只看該作者
Technical aspects of aortic surgery for Marfan syndrome,Our total experience of aortic surgery for Marfan syndrome includes 281 patients and covers either true aneurysm or dissections of the ascending aorta, the aortic arch and abdominal aorta.
32#
發(fā)表于 2025-3-27 02:10:47 | 只看該作者
https://doi.org/10.1007/978-3-642-72508-1aneurysm; blood; blood vessel; cardiovascular; heart; heart disease; pathogenesis; skeleton; therapy; tissue;
33#
發(fā)表于 2025-3-27 06:12:54 | 只看該作者
34#
發(fā)表于 2025-3-27 10:36:09 | 只看該作者
35#
發(fā)表于 2025-3-27 17:20:08 | 只看該作者
6 Magnetic confinement fusion: tokamak,tory that led to the recent discovery of the cause of the Marfan syndrome — an expedition that I always thought would lead to the pinnacle of any medical scientist’s career, preferably mine. Having found the cause, however, we now realize that it is a false peak, just a foothill on the way to the su
36#
發(fā)表于 2025-3-27 18:19:24 | 只看該作者
37#
發(fā)表于 2025-3-28 00:00:05 | 只看該作者
7 Magnetic confinement fusion: stellarator,nt that McKusick (4) described the clinical presentation in detail and, moreover, identified the syndrome as an inherited connective tissue disease. Despite the heterogeneity in the phenotypic expression of the disease, Marfan syndrome was subsequently characterized as an autosomal dominant connecti
38#
發(fā)表于 2025-3-28 03:49:53 | 只看該作者
1.1 Principles of fission reactors,ating or dissecting diseases of the thoracic aorta (4, 7). Thus, connective tissue disorders involving either elastic tissue degeneration or disturbed collagen synthesis are widely associated with an increased fragility of the aortic wall, as encountered with degenerative tissue abnormalities, in pa
39#
發(fā)表于 2025-3-28 09:19:22 | 只看該作者
Nuclear Energy Development in Asiaities (9). The major cardiovascular components of the disease were described by Etter and Baer in 1943 (1, 5). Marfan syndrome occurs in patients who are heterozygous for a mutation that alters one or more components of the extracellular matrix (12, 22). It has been shown that in Marfan syndrome the
40#
發(fā)表于 2025-3-28 13:21:39 | 只看該作者
The Spallation - Fission Symbiontotentially lethal cardiovascular manifestations of the disease (3–5), and only recently has it become evident that these are the main determinants of prognosis of affected individuals (6). If uncorrected, these manifestations can lead to severe disability or death at a young age. Although prolapse o
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