{"created":"2023-05-15T09:02:42.450051+00:00","id":3572,"links":{},"metadata":{"_buckets":{"deposit":"6c158195-bbb6-46d8-a81b-85aced8b60a7"},"_deposit":{"created_by":3,"id":"3572","owners":[3],"pid":{"revision_id":0,"type":"depid","value":"3572"},"status":"published"},"_oai":{"id":"oai:hirosaki.repo.nii.ac.jp:00003572","sets":["557:561:635"]},"author_link":["11107","11078","11074","11108","11099","11098","11111","11109","11103","11095","11104","11096","11105","11110","11102","11097","11101","11082"],"item_5_alternative_title_21":{"attribute_name":"その他のタイトル","attribute_value_mlt":[{"subitem_alternative_title":"TREATMENT OUTCOME OF IMATINIB MESYLATE FOR CHRONIC MYELOGENOUS LEUKEMIA IN 11 CASES"}]},"item_5_alternative_title_22":{"attribute_name":"タイトル（ヨミ）","attribute_value_mlt":[{"subitem_alternative_title":"マンセイ コツズイセイ ハッケツビョウ ニ メシルサン イマチニブ オ トウヨシタ 11レイ ノ チリョウ 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3以上の皮疹,筋肉痛,血液毒性を認めた5例で休薬を要した他は重篤な有害事象を認めず,imatinib継続が可能だった.Imatinibは特に慢性期症例では軽微な有害事象のみで初期投与量が維持され,優れた細胞遺伝学的効果を得ることができた.","subitem_description_type":"Abstract"}]},"item_5_full_name_2":{"attribute_name":"著者(ヨミ)","attribute_value_mlt":[{"nameIdentifiers":[{"nameIdentifier":"11101","nameIdentifierScheme":"WEKO"}],"names":[{"name":"イシグロ, アツシ"}]},{"nameIdentifiers":[{"nameIdentifier":"11102","nameIdentifierScheme":"WEKO"}],"names":[{"name":"コマツ, トモコ"}]},{"nameIdentifiers":[{"nameIdentifier":"11103","nameIdentifierScheme":"WEKO"}],"names":[{"name":"ヤマガタ, カズフミ"}]},{"nameIdentifiers":[{"nameIdentifier":"11104","nameIdentifierScheme":"WEKO"}],"names":[{"name":"タマイ, ヨシコ"}]},{"nameIdentifiers":[{"nameIdentifier":"11105","nameIdentifierScheme":"WEKO"}],"names":[{"name":"タカミ, ヒデキ"}]},{"nameIdentifiers":[{"nameIdentifier":"11078","nameIdentifierScheme":"WEKO"}],"names":[{"name":"ムナカタ, 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