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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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發(fā)表于 2025-3-21 17:46:53 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Cardiovascular Aspects of Marfan Syndrome
編輯R. Hetzer,P. Gehle,J. Ennker
視頻videohttp://file.papertrans.cn/222/221901/221901.mp4
圖書封面Titlebook: Cardiovascular Aspects of Marfan Syndrome;  R. Hetzer,P. Gehle,J. Ennker Book 1995 Dr. Dietrich Steinkopff Verlag GmbH & Co. KG, Darmstadt
描述Marfan Syndrome is a hereditary disorder of connective tissue which primarily affects the eyes, skeleton, blood vessels, and various structures of the heart. .Since 1943, when the cardiovascular manifestations of Marfan Syndrome were first described, understanding of its nature, diagnostic tools, and surgical treatment have been remarkably improved. Although the specific surgical procedures have reached an advanced standard and general acceptance, many questions remain unanswered and have given rise to ongoing controversy. .Cardiovascular Aspects of Marfan Syndrome. presents the advances in understanding the cause and pathogenesis of Marfan Syndrome and its current specific surgical therapy.
出版日期Book 1995
關鍵詞aneurysm; blood; blood vessel; cardiovascular; heart; heart disease; pathogenesis; skeleton; therapy; tissue;
版次1
doihttps://doi.org/10.1007/978-3-642-72508-1
isbn_softcover978-3-642-72510-4
isbn_ebook978-3-642-72508-1
copyrightDr. Dietrich Steinkopff Verlag GmbH & Co. KG, Darmstadt 1995
The information of publication is updating

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發(fā)表于 2025-3-21 23:50:29 | 只看該作者
,Cardiovascular pathology in Marfan syndrome — An overview,findings include myopia and subluxation of the lenses. The most serious and often life-threatening manifestations of Marfan syndrome occur in the cardiovascular system. Aortic root dilation and aneurysm formation of the ascending aorta are the most prominent and aortic wall rupture, with or without
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6 Magnetic confinement fusion: tokamak,n chromosome 15, but instead is most probably caused by mutations in the closely-related gene on chromosome 5 (9). Another related disease is familial annuloaortic ectasia for which only preliminary data exists on the molecular defect.
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發(fā)表于 2025-3-22 11:45:22 | 只看該作者
7 Magnetic confinement fusion: stellarator,findings include myopia and subluxation of the lenses. The most serious and often life-threatening manifestations of Marfan syndrome occur in the cardiovascular system. Aortic root dilation and aneurysm formation of the ascending aorta are the most prominent and aortic wall rupture, with or without
6#
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res of the heart. .Since 1943, when the cardiovascular manifestations of Marfan Syndrome were first described, understanding of its nature, diagnostic tools, and surgical treatment have been remarkably improved. Although the specific surgical procedures have reached an advanced standard and general
9#
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6 Magnetic confinement fusion: tokamak,cal 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 summit. The presentations and discussion at this meeting will indicate how much further we all need to climb to achieve the goal of total understanding of this complex disorder.
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