Hereditary hemorrhagic telangiectasia in Japanese patients
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- KOMIYAMA Masaki
- Department of Neurosurgery, Osaka City General Hospital
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- NISHIKAWA Misao
- Department of Neurosurgery, Osaka City General Hospital
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- YASUI Toshihiro
- Department of Neurosurgery, Osaka City General Hospital
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- OTSUKA Masato
- Department of Cardiology, Osaka City General Hospital
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- HAZE Kazuo
- Department of Cardiology, Osaka City General Hospital
書誌事項
- タイトル別名
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- Moyamoya Disease and Coronary Artery Disease. Case Report.
- —Case Report—
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説明
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 epi- cardial 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.<br>
収録刊行物
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- Neurologia medico-chirurgica
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Neurologia medico-chirurgica 41 (1), 37-41, 2001
一般社団法人 日本脳神経外科学会
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詳細情報 詳細情報について
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- CRID
- 1390001205048830336
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- NII論文ID
- 110002281330
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- NII書誌ID
- AN00358613
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- ISSN
- 14345161
- 13498029
- 04708105
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- COI
- 1:STN:280:DC%2BD3M7ltVegtg%3D%3D
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- NDL書誌ID
- 025154650
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- PubMed
- 11218639
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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- JaLC
- NDLサーチ
- Crossref
- PubMed
- CiNii Articles
- OpenAIRE
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- 抄録ライセンスフラグ
- 使用不可