{"_buckets": {"deposit": "3fe494ca-189b-4b7a-bd92-bd9c68c39d43"}, "_deposit": {"id": "24850", "owners": [], "pid": {"revision_id": 0, "type": "depid", "value": "24850"}, "status": "published"}, "_oai": {"id": "oai:nagoya.repo.nii.ac.jp:00024850", "sets": ["501"]}, "author_link": ["73906", "73907", "73908", "73909", "73910", "73911"], "item_10_biblio_info_6": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2017-08", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "8", "bibliographicPageEnd": "1409", "bibliographicPageStart": "1405", "bibliographicVolumeNumber": "33", "bibliographic_titles": [{"bibliographic_title": "Childs Nervous System", "bibliographic_titleLang": "en"}]}]}, "item_10_description_4": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "Background Focal cerebral arteriopathy includes unifocal or multifocal lesions that are unilateral or bilateral. Large- and/or medium-sized vessels are involved and can be visualized on angiography. Case report We report a case of cerebral infarction in a 9-yearold Japanese female who presented with a transient ischemic attack. Steno-occlusion involving the distal part of the internal carotid artery, proximal middle cerebral artery, and anterior cerebral artery was observed. Digital subtraction angiography demonstrated a beaded appearance in the cervical portion of the diseased internal carotid artery. Revascularization surgery was performed 45 days after the onset. A new infarction appeared on the other side of the anterior cerebral artery territory 7 months after the first onset. Antiplatelets and vasodilators were administered, and no progression was observed during 18 months of follow-up. Genetic analysis did not show ring finger protein 213 (RNF213)- related moyamoya disease, and pathological examination revealed no characteristics of fibromuscular dysplasia. Conclusion The radiological and genetic features coincided with focal cerebral arteriopathy, which is a distinct entity from fibromuscular dysplasia and RNF213-related moyamoya disease.", "subitem_description_language": "en", "subitem_description_type": "Abstract"}]}, "item_10_identifier_60": {"attribute_name": "URI", "attribute_value_mlt": [{"subitem_identifier_type": "DOI", "subitem_identifier_uri": "http://doi.org/10.1007/s00381-017-3451-9"}, {"subitem_identifier_type": "HDL", "subitem_identifier_uri": "http://hdl.handle.net/2237/27070"}]}, "item_10_publisher_32": {"attribute_name": "出版者", "attribute_value_mlt": [{"subitem_publisher": "Springer", "subitem_publisher_language": "en"}]}, "item_10_relation_11": {"attribute_name": "DOI", "attribute_value_mlt": [{"subitem_relation_type": "isVersionOf", "subitem_relation_type_id": {"subitem_relation_type_id_text": "https://doi.org/10.1007/s00381-017-3451-9", "subitem_relation_type_select": "DOI"}}]}, "item_10_rights_12": {"attribute_name": "権利", "attribute_value_mlt": [{"subitem_rights": "The final publication is available at Springer via http://doi.org/10.1007/s00381-017-3451-9", "subitem_rights_language": "en"}]}, "item_10_select_15": {"attribute_name": "著者版フラグ", "attribute_value_mlt": [{"subitem_select_item": "author"}]}, "item_10_source_id_7": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "0256-7040", "subitem_source_identifier_type": "PISSN"}]}, "item_1615787544753": {"attribute_name": "出版タイプ", "attribute_value_mlt": [{"subitem_version_resource": "http://purl.org/coar/version/c_ab4af688f83e57aa", "subitem_version_type": "AM"}]}, "item_access_right": {"attribute_name": "アクセス権", "attribute_value_mlt": [{"subitem_access_right": "open access", "subitem_access_right_uri": "http://purl.org/coar/access_right/c_abf2"}]}, "item_creator": {"attribute_name": "著者", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Yoshio, Araki", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "73906", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Yasushi, Takagi", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "73907", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Yohei, Mineharu", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "73908", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Hatasu, Kobayashi", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "73909", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Susumu, Miyamoto", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "73910", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Toshihiko, Wakabayashi", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "73911", "nameIdentifierScheme": "WEKO"}]}]}, "item_files": {"attribute_name": "ファイル情報", "attribute_type": "file", "attribute_value_mlt": [{"accessrole": "open_date", "date": [{"dateType": "Available", "dateValue": "2018-08-01"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "manuscript_for_child_nervous_system_version.pdf", "filesize": [{"value": "4.0 MB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_note", "mimetype": "application/pdf", "size": 4000000.0, "url": {"label": "manuscript_for_child_nervous_system_version.pdf ファイル公開日:2018/08/01", "objectType": "fulltext", "url": "https://nagoya.repo.nii.ac.jp/record/24850/files/manuscript_for_child_nervous_system_version.pdf"}, "version_id": "a4b3b502-5cc0-4955-b34b-45f53314047e"}]}, "item_keyword": {"attribute_name": "キーワード", "attribute_value_mlt": [{"subitem_subject": "Focal cerebral arteriopathy", "subitem_subject_scheme": "Other"}, {"subitem_subject": "RNF213", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Moyamoya disease", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Fibromuscular dysplasia", "subitem_subject_scheme": "Other"}]}, "item_language": {"attribute_name": "言語", "attribute_value_mlt": [{"subitem_language": "eng"}]}, "item_resource_type": {"attribute_name": "資源タイプ", "attribute_value_mlt": [{"resourcetype": "journal article", "resourceuri": "http://purl.org/coar/resource_type/c_6501"}]}, "item_title": "Rapid Contralateral Progression of Focal Cerebral Arteriopathy Distinguished from RNF213-related moyamoya disease and fibromuscular dysplasia", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "Rapid Contralateral Progression of Focal Cerebral Arteriopathy Distinguished from RNF213-related moyamoya disease and fibromuscular dysplasia", "subitem_title_language": "en"}]}, "item_type_id": "10", "owner": "1", "path": ["501"], "permalink_uri": "http://hdl.handle.net/2237/27070", "pubdate": {"attribute_name": "PubDate", "attribute_value": "2017-11-07"}, "publish_date": "2017-11-07", "publish_status": "0", "recid": "24850", "relation": {}, "relation_version_is_last": true, "title": ["Rapid Contralateral Progression of Focal Cerebral Arteriopathy Distinguished from RNF213-related moyamoya disease and fibromuscular dysplasia"], "weko_shared_id": -1}