subarachnoid cerebral hemorrhageとは 意味・読み方・使い方

(2) The cerebrovascular disorder is cerebral infarction, cerebral hemorrhage, subarachnoid hemorrhage or cerebral edema in the prophylactic or therapeutic agent described in (1).例文帳に追加

（２） 脳血管障害が脳梗塞、脳出血、くも膜下出血又は脳浮腫である前記（１）記載の予防又は治療剤。 - 特許庁

(4) The disease based on cerebrovascular disorder is cerebral infarction, cerebral hemorrhage, subarachnoid hemorrhage or cerebral edema, in the health food for preventing or treating diseases based on cerebrovascular disorder described in (3).例文帳に追加

（４）脳血管障害に基づく疾患が脳梗塞、脳出血、くも膜下出血又は脳浮腫である前記（３）記載の脳血管障害に基づく疾患の予防又は治療用健康食品。 - 特許庁

To provide a Chinese medicine without having toxicity and side-effects for treating cerebrovascular diseases(CVD) such as 'cerebral infarction', 'cerebral thrombosis', 'cerebral embolism', 'cerebral hemorrhage', 'subarachnoid hemorrage' and the like.例文帳に追加

毒、副作用のない“脳血栓（ｃｅｒｅｂｒａｌ ｉｎｆａｒｃｔｉｏｎ）、脳血栓形成（ｃｅｒｅｂｒａｌ ｔｈｒｏｍｂｏｓｉｓ）、脳栓塞（ｃｅｒｅｂｒａｌ ｅｍｂｏｌｉｓｍ）、脳出血（ｃｅｒｅｂｒａｌ ｈｅｍｏｒｒｈａｇｅ）、蛛网膜下腔出血（ｓｕｂａｒａｃｈｎｏｉｄ ｈｅｍｏｒｒｈａｇｅ）”などの脳血管病気（ＣＶＤ）を治療する漢方薬。 - 特許庁

As a result of the investigation, it has been clarified that the risk detection based on 8 genetic polymorphisms for atherothrombotic cerebral infarction, 9 genetic polymorphisms for cerebral hemorrhage and 10 genetic polymorphisms for subarachnoid hemorrhage in addition to the conventional risk factors for cerebrovascular disorder is useful for the primary and secondary prevention of cerebrovascular disorder.例文帳に追加

その結果、従来の脳血管障害の危険因子に加え、アテローム血栓性脳梗塞では８個の遺伝子多型、脳出血では９個の遺伝子多型、クモ膜下出血では１０個の遺伝子多型を加えたリスク検出法は、脳血管障害の一次、二次予防に有用であることが示された。 - 特許庁

Two hundred and two genetic polymorphisms relating to 152 candidate genes were measured on 1,141 patients of cerebrovascular disorder (636 patients of atherothrombotic cerebral infarction, 282 patients of cerebral hemorrhage and 223 patients of subarachnoid hemorrhage) and 2,010 controls to detect genetic polymorphisms significantly relating to the onset of these 3 diseases.例文帳に追加

１１４１人の脳血管障害患者（アテローム血栓性脳梗塞患者６３６人、脳出血患者２８２人、クモ膜下出血患者２２３人）とコントロール者２０１０人とについて、１５２個の候補遺伝子に関し２０２個の遺伝子多型を測定し、上記３疾患の発症に有意に関連する遺伝子多型を検出した。 - 特許庁