標(biāo)題: Titlebook: Cardiovascular Aspects of Marfan Syndrome; R. Hetzer,P. Gehle,J. Ennker Book 1995 Dr. Dietrich Steinkopff Verlag GmbH & Co. KG, Darmstadt [打印本頁] 作者: 淺吟低唱 時間: 2025-3-21 17:46
書目名稱Cardiovascular Aspects of Marfan Syndrome影響因子(影響力)
書目名稱Cardiovascular Aspects of Marfan Syndrome影響因子(影響力)學(xué)科排名
書目名稱Cardiovascular Aspects of Marfan Syndrome網(wǎng)絡(luò)公開度
書目名稱Cardiovascular Aspects of Marfan Syndrome網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Cardiovascular Aspects of Marfan Syndrome被引頻次
書目名稱Cardiovascular Aspects of Marfan Syndrome被引頻次學(xué)科排名
書目名稱Cardiovascular Aspects of Marfan Syndrome年度引用
書目名稱Cardiovascular Aspects of Marfan Syndrome年度引用學(xué)科排名
書目名稱Cardiovascular Aspects of Marfan Syndrome讀者反饋
書目名稱Cardiovascular Aspects of Marfan Syndrome讀者反饋學(xué)科排名
作者: comely 時間: 2025-3-21 23:50
,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 作者: wangle 時間: 2025-3-22 01:07 作者: Sinus-Node 時間: 2025-3-22 07:25
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.作者: flammable 時間: 2025-3-22 11:45
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 作者: FEMUR 時間: 2025-3-22 16:24 作者: FEMUR 時間: 2025-3-22 19:39 作者: Psychogenic 時間: 2025-3-23 00:29
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 作者: 考博 時間: 2025-3-23 04:27
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.作者: 壓倒 時間: 2025-3-23 06:56 作者: 周年紀(jì)念日 時間: 2025-3-23 10:56
Reaction and Reactor Systematicsarfanoid” patients, i.e., patients who exhibited typical manifestations in three different organ systems (cardiovascular, ocular, skeletal, or other organ systems) while not completely fulfilling the diagnostic criteria for Marfan syndrome (22).作者: GENUS 時間: 2025-3-23 15:21
Toward understanding cause and pathogenesis of Towards Marfan syndrome,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.作者: 仔細(xì)檢查 時間: 2025-3-23 21:19
,Annulo-aortic ectasia — with special reference to total repair of patients with Marfan syndrome,that time were not good (2). Figure 2 shows the same patient 21 months after the operation. A huge aneurysm is evident which developed from the rim of the ascending aorta left in place above the coronary ostia. Therefore, we initiated our own technique and never used the original Bentall method (1).作者: glomeruli 時間: 2025-3-23 22:36
Results of cardiovascular surgery for Marfan syndrome in Berlin,arfanoid” patients, i.e., patients who exhibited typical manifestations in three different organ systems (cardiovascular, ocular, skeletal, or other organ systems) while not completely fulfilling the diagnostic criteria for Marfan syndrome (22).作者: 警告 時間: 2025-3-24 05:16
The mechanism and prevention of aortic dissection in Marfan syndrome, elastic fibers ordinarily prominent in the aortic media appear disorganized and fragmented. This defect, presumably induced by biochemical changes, renders the aorta susceptible not only to dilatation, but also to dissection (22) which eventually leads to the demise of 90% of those who suffer from this disease.作者: tattle 時間: 2025-3-24 09:22
,Marfan syndrome and pregnancy complicated by an acute dissecting aortic aneurysm DeBakey type I — A was therefore transferred to our cardiology department for further investigation. She was 2.06 m in height and had a typical Marfan-habit (pes planus, thoracic lordosis, pectus deformity, joint hypermobility, arachnodactyly) (Fig. 1). Nevertheless, the diagnosis of Marfan syndrome had not been made previously.作者: 名字的誤用 時間: 2025-3-24 12:43
Book 1995, 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.作者: fibula 時間: 2025-3-24 18:34
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.978-3-642-72510-4978-3-642-72508-1作者: 柔美流暢 時間: 2025-3-24 19:45 作者: 細(xì)頸瓶 時間: 2025-3-25 03:11
The (D-T) Fusion-Fission Symbiontfor composite aortic root replacement, significant improvements for Marfan patients could be achieved. This was especially the case if they were operated upon electively, usually before the diameter of the ascending aorta reached 6 cm (9).作者: 偏狂癥 時間: 2025-3-25 06:36 作者: Electrolysis 時間: 2025-3-25 10:08
Aortic disease in Marfan syndrome: surgery, results, and special aspects,for composite aortic root replacement, significant improvements for Marfan patients could be achieved. This was especially the case if they were operated upon electively, usually before the diameter of the ascending aorta reached 6 cm (9).作者: 效果 時間: 2025-3-25 14:30 作者: 針葉類的樹 時間: 2025-3-25 18:33 作者: 保守 時間: 2025-3-25 22:27 作者: 職業(yè) 時間: 2025-3-26 02:18 作者: interpose 時間: 2025-3-26 07:05
7 Magnetic confinement fusion: stellarator,Dr. Hetzer had asked me to report briefly on the history of operating for Marfan syndrome. This is a rather gloomy subject!作者: fledged 時間: 2025-3-26 09:47
Nuclear Energy Development in AsiaOur 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.作者: ELUDE 時間: 2025-3-26 15:06
Cardiovascular disease in Marfan patients in infancy and childhood,The case of Gabrielle P, aged 5? months, gave no indication that there was any cardiovascular involvement; and there is now some doubt that Marfan patient actually had the eponymous disease [6, 8].作者: VEST 時間: 2025-3-26 19:50 作者: Aspiration 時間: 2025-3-26 22:43
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.作者: Lament 時間: 2025-3-27 02:10
https://doi.org/10.1007/978-3-642-72508-1aneurysm; blood; blood vessel; cardiovascular; heart; heart disease; pathogenesis; skeleton; therapy; tissue; 作者: MELON 時間: 2025-3-27 06:12 作者: 溺愛 時間: 2025-3-27 10:36 作者: 閃光你我 時間: 2025-3-27 17:20
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作者: 反對 時間: 2025-3-27 18:19 作者: 剛開始 時間: 2025-3-28 00:00
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作者: Torrid 時間: 2025-3-28 03:49
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作者: Host142 時間: 2025-3-28 09:19
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作者: Debrief 時間: 2025-3-28 13:21
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作者: 帽子 時間: 2025-3-28 17:31
The (D-T) Fusion-Fission Hybridwe used the supracoronary resection technique in 9 cases. Figure 1 shows the first patient ever successfully operated in Finland. Our late results at that time were not good (2). Figure 2 shows the same patient 21 months after the operation. A huge aneurysm is evident which developed from the rim of作者: 梯田 時間: 2025-3-28 20:53 作者: Ossification 時間: 2025-3-29 02:25 作者: 為現(xiàn)場 時間: 2025-3-29 04:53
Reaction and Reactor Systematicsas established at the Conference on International Nosology of Heritable Disorders of Connective Tissue held in Berlin in 1986 (1, 25) and so-called “marfanoid” patients, i.e., patients who exhibited typical manifestations in three different organ systems (cardiovascular, ocular, skeletal, or other o作者: 種屬關(guān)系 時間: 2025-3-29 08:06 作者: 植物茂盛 時間: 2025-3-29 14:32
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 particular in patients with Marfan syndrome (1, 3).作者: 定點 時間: 2025-3-29 17:27 作者: deactivate 時間: 2025-3-29 21:46 作者: 取回 時間: 2025-3-30 00:55
,Cardiovascular pathology in Marfan syndrome — An overview,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作者: anniversary 時間: 2025-3-30 07:01
Relevance of cystic medial degeneration in cardiac surgery,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作者: 態(tài)度暖昧 時間: 2025-3-30 10:55
The mechanism and prevention of aortic dissection in Marfan syndrome,ities (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作者: 意外 時間: 2025-3-30 12:24 作者: expound 時間: 2025-3-30 18:44 作者: 不容置疑 時間: 2025-3-30 22:17 作者: aspersion 時間: 2025-3-31 00:59
Aortic disease in Marfan syndrome: surgery, results, and special aspects, fibrillin, an essential structural protein of elastic fibers, is synthesized. This leads to a disarray of fibers with resultant hyperelasticity and weakness. The expression of the disease is pleiomorphic, but in general it affects the ocular, skeletal and/or cardiovascular systems. The complication作者: Debility 時間: 2025-3-31 07:49
Results of cardiovascular surgery for Marfan syndrome in Berlin,as established at the Conference on International Nosology of Heritable Disorders of Connective Tissue held in Berlin in 1986 (1, 25) and so-called “marfanoid” patients, i.e., patients who exhibited typical manifestations in three different organ systems (cardiovascular, ocular, skeletal, or other o作者: left-ventricle 時間: 2025-3-31 11:07 作者: narcissism 時間: 2025-3-31 13:35
Xianghong Lin,Tiandou Hu,Xiangwen Wang,Han Lulegendary duel between the Egyptian Pharaoh and his magicians (Alchemists) on one side, and Moses and his brother Aaron on the other, as is vividly narrated in the Bible, must have realised that people (at least those living at, or near the eternal battlefields of the Middle East) have always had kn作者: dandruff 時間: 2025-3-31 18:36 作者: podiatrist 時間: 2025-3-31 22:34 作者: 都相信我的話 時間: 2025-4-1 03:13 作者: abracadabra 時間: 2025-4-1 08:10 作者: 翅膀拍動 時間: 2025-4-1 11:56
ublic administrations, consultancy firms and nongovernmental organizations insights into counterfactual impact evaluation methods and the potential of data-based policy and program evaluation.?.978-3-030-08703-6978-3-319-78461-8
