Moyamoya Disease and Coronary Artery Disease
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概要
- 論文の詳細を見る
A 26-year-old female with idiopathic moyamoya disease developed chest pain with concomitant ST depression on electrocardiography. Coronary angiography detected no stenotic lesions in the epicardial coronary arteries. The clinical diagnosis was vasospastic angina pectoris. She was medicated with calcium antagonists, which reduced the frequency of chest pain episodes. Angina pectoris is a rare occurrence in young patients with moyamoya disease. Coronary artery disease and moyamoya disease may have common etiological factors.
- 日本脳神経外科学会の論文
- 2001-01-15
著者
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小宮山 雅樹
大阪市立総合医療センター脳神経外科
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Otsuka Masato
Department Of Pathology Osaka City University Graduate School Of Medicine
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KOMIYAMA Masaki
Department of Neurosurgery,Osaka City General Hospital
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YASUI Toshihiro
Department of Neurosurgery,Osaka City General Hospital
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Nishikawa Misao
Department of Neurosurgery, Osaka city University Graduate School of Medicine
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Nishikawa Misao
大阪市立大学 医研究脳神経外科学
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Nishikawa Misao
Department Of Neurosurgery Osaka City University Graduate School Of Medicine
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Haze Kazuo
Department Of Cardiology Osaka City General Hospital
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Haze Kazuo
Department Of Cardiology National Cardiovascular Center
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Yamada Osamu
Department Of Cardiovascular Dynamics National Cardiovascular Center Research Institute
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Otsuka Masato
Department Of Biochemistry Faculty Of Pharmaceutical Sciences Okayama University
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Otsuka Masato
Department Of Cardiology Osaka City General Hospital
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Yasui Toshihiro
Department Of Neurosurgery Osaka City General Hospital
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Komiyama Masaki
Department Of Neurosurgery Baba Memorial Hospital
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Yasui Toshihiro
Department Of Neurosurgery Baba Memorial Hospital
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Ishiguro Tomoya
Department Of Neurosurgery Osaka City General Hospital
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Nishikawa Misao
Department Of Neurosurgery Osaka City General Hospital
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