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Pathology of the Eisenmenger syndrome and primary pulmonary hypertension.

作者信息

Wagenvoort C A, Wagenvoort N

出版信息

Adv Cardiol. 1974;11(00):123-30. doi: 10.1159/000395210.

DOI:10.1159/000395210
PMID:4137876
Abstract
摘要

相似文献

1
Pathology of the Eisenmenger syndrome and primary pulmonary hypertension.艾森曼格综合征和原发性肺动脉高压的病理学
Adv Cardiol. 1974;11(00):123-30. doi: 10.1159/000395210.
2
Eisenmenger complex.
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3
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A problem in pulmonary hypertension. 2. The final course and autopsy findings. A clinicopathologic conference from the Division of Pulmonary Diseases, Hahnemann Medical College and Hospital, Philadelphia.
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Primary and chronic thromboembolic pulmonary hypertension. Clinical and pathoanatomic observations.原发性和慢性血栓栓塞性肺动脉高压。临床及病理解剖学观察
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Idiopathic pulmonary hypertension in infancy and childhood. Microangiographic and histological observations in five cases.婴幼儿特发性肺动脉高压。5例微血管造影及组织学观察
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Eisenmenger syndrome and idiopathic pulmonary arterial hypertension: do parenchymal lung changes reflect aetiology?艾森曼格综合征与特发性肺动脉高压：肺实质改变能反映病因吗？
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Letter by asosingh et Al regarding article, "circulating endothelial progenitor cells in patients with eisenmenger syndrome and idiopathic pulmonary arterial hypertension".阿索辛等人就“艾森曼格综合征和特发性肺动脉高压患者循环内皮祖细胞”一文所写的信。
Circulation. 2009 Mar 10;119(9):e230; author reply e231. doi: 10.1161/CIRCULATIONAHA.108.800961.
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Br Heart J. 1978 Aug;40(8):825-31. doi: 10.1136/hrt.40.8.825.

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Functional status of patients with large ventricular septal defect and pulmonary vascular disease 6 to 16 years after surgical closure of their defect in childhood.童年期大型室间隔缺损及肺血管疾病患者在缺损手术闭合6至16年后的功能状态。
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