familial hemiplegic migraine
- 网络家族性偏瘫性偏头痛;家族性偏瘫型偏头痛;性偏头痛
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Single - fiber EMG in familial hemiplegic migraine
家族性偏瘫性偏头痛的单纤维肌电图
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~ 1H-MRS alterations in the cerebellum of patients with familial hemiplegic migraine type 1
1型家族性偏瘫性偏头痛患者小脑的~1H-MRS改变
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The identification of familial hemiplegic migraine ( FHM ) calcium channel α 1A ( CACNA1A ) has set off an upsurge of research into migraine molecular genetics .
对家族性偏瘫型偏头痛(FHM)家系CACNA1A基因的鉴定,掀起了偏头痛分子遗传学研究的热潮。
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The finding of mutations in the Na + / K + - ATPase α - subunit gene in familial hemiplegic migraine ( FHM ) is a great breakthrough in the research of migraine genetics .
家族性偏瘫型偏头痛(familialhemiplegicmigraine,FHM)中Na+/K+ATP酶α2亚基ATP1A2基因突变的发现,是偏头痛遗传学研究的重大突破。
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This article reviews the relationship between SCD and neurobiological mechanism of migraine , particular expounding the significance in the gene mutations of familial hemiplegic migraine , CSD in migraine pathophysiological mechanisms and their prophylactic treatment .
文章就CSD与偏头痛神经生物学机制关第进行了综述,重点阐述了家族性偏瘫型偏头痛的基因突变以及CSD在偏头痛病理生理学机制和预防性治疗等方面的意义。