{"_buckets": {"deposit": "301591c7-fe01-40f7-81e6-10685724b2f7"}, "_deposit": {"id": "21287", "owners": [], "pid": {"revision_id": 0, "type": "depid", "value": "21287"}, "status": "published"}, "_oai": {"id": "oai:niigata-u.repo.nii.ac.jp:00021287", "sets": ["456", "1183"]}, "item_7_alternative_title_1": {"attribute_name": "その他のタイトル", "attribute_value_mlt": [{"subitem_alternative_title": "Hereditary Lipo-muscular Atrophy with Joint Contracture, Skin Eruptions and Hyper-γ-Globulinemia : A New Syndrome"}]}, "item_7_biblio_info_6": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "1991-08", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "8", "bibliographicPageEnd": "508", "bibliographicPageStart": "503", "bibliographicVolumeNumber": "105", "bibliographic_titles": [{"bibliographic_title": "新潟医学会雑誌"}, {"bibliographic_title": "新潟医学会雑誌", "bibliographic_titleLang": "en"}]}]}, "item_7_description_4": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "Two siblings with decreased subcutaneous adipose tissue, muscular atrophy, joint contractures, recurrent skin eruptions and hyper-γ-globulinemia are reported. Patients showed reduced natural killer cell activity. The skin eruptions disappeared with prednisolone therapy. The clinical symptoms of these patients share some features with partial lipodystrophy but our patients are considered to be distinct from partial lipodystrophy since muscular atrophy, joint contractures and recurrent skin eruptions haye not been found in patients with partial lipodystrophy. Other Japanese nineteen patients with similar clinical manifestations have been reported. We propose that these patients show a distinct clinical entity.", "subitem_description_type": "Abstract"}]}, "item_7_full_name_3": {"attribute_name": "著者別名", "attribute_value_mlt": [{"nameIdentifiers": [{"nameIdentifier": "130348", "nameIdentifierScheme": "WEKO"}], "names": [{"name": "Tanaka, Masami"}]}]}, "item_7_publisher_7": {"attribute_name": "出版者", "attribute_value_mlt": [{"subitem_publisher": "新潟医学会"}]}, "item_7_select_19": {"attribute_name": "著者版フラグ", "attribute_value_mlt": [{"subitem_select_item": "publisher"}]}, "item_7_source_id_11": {"attribute_name": "書誌レコードID", "attribute_value_mlt": [{"subitem_source_identifier": "AN00182415", "subitem_source_identifier_type": "NCID"}]}, "item_7_source_id_9": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "00290440", "subitem_source_identifier_type": "ISSN"}]}, "item_creator": {"attribute_name": "著者", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "田中, 正美"}], "nameIdentifiers": [{"nameIdentifier": "130347", "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": "2019-08-16"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "105(8)_503-508.pdf", "filesize": [{"value": "3.5 MB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 3500000.0, "url": {"label": "105(8)_503-508.pdf", "url": "https://niigata-u.repo.nii.ac.jp/record/21287/files/105(8)_503-508.pdf"}, "version_id": "08a727b9-5d5e-44ca-a99a-86b5eb6e4284"}]}, "item_keyword": {"attribute_name": "キーワード", "attribute_value_mlt": [{"subitem_subject": "lipodystrophy", "subitem_subject_scheme": "Other"}, {"subitem_subject": "eruption", "subitem_subject_scheme": "Other"}, {"subitem_subject": "hyper-γ-globulinemia", "subitem_subject_scheme": "Other"}, {"subitem_subject": "natural killer", "subitem_subject_scheme": "Other"}, {"subitem_subject": "muscular atrophy", "subitem_subject_scheme": "Other"}, {"subitem_subject": "リポジストロフィー", "subitem_subject_scheme": "Other"}, {"subitem_subject": "発診", "subitem_subject_scheme": "Other"}, {"subitem_subject": "高γ-グロブリン血症", "subitem_subject_scheme": "Other"}, {"subitem_subject": "ナチュラルキラー", "subitem_subject_scheme": "Other"}, {"subitem_subject": "筋萎縮", "subitem_subject_scheme": "Other"}]}, "item_language": {"attribute_name": "言語", "attribute_value_mlt": [{"subitem_language": "jpn"}]}, "item_resource_type": {"attribute_name": "資源タイプ", "attribute_value_mlt": [{"resourcetype": "departmental bulletin paper", "resourceuri": "http://purl.org/coar/resource_type/c_6501"}]}, "item_title": "関節拘縮, 結節性紅斑, 高γ-グロブリン血症を伴う常染色体劣性遺伝形式を示す脂肪筋萎縮症 : 新しい症候群の提唱", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "関節拘縮, 結節性紅斑, 高γ-グロブリン血症を伴う常染色体劣性遺伝形式を示す脂肪筋萎縮症 : 新しい症候群の提唱"}, {"subitem_title": "関節拘縮, 結節性紅斑, 高γ-グロブリン血症を伴う常染色体劣性遺伝形式を示す脂肪筋萎縮症 : 新しい症候群の提唱", "subitem_title_language": "en"}]}, "item_type_id": "7", "owner": "1", "path": ["456", "1183"], "permalink_uri": "http://hdl.handle.net/10191/39331", "pubdate": {"attribute_name": "公開日", "attribute_value": "2016-03-10"}, "publish_date": "2016-03-10", "publish_status": "0", "recid": "21287", "relation": {}, "relation_version_is_last": true, "title": ["関節拘縮, 結節性紅斑, 高γ-グロブリン血症を伴う常染色体劣性遺伝形式を示す脂肪筋萎縮症 : 新しい症候群の提唱"], "weko_shared_id": null}