WEKO3
インデックスリンク
アイテム
{"_buckets": {"deposit": "ea2dc6b5-a0eb-4f60-b321-5b883888a85e"}, "_deposit": {"created_by": 3, "id": "26623", "owners": [3], "pid": {"revision_id": 0, "type": "depid", "value": "26623"}, "status": "published"}, "_oai": {"id": "oai:kanazawa-u.repo.nii.ac.jp:00026623", "sets": ["1763"]}, "author_link": ["44696", "44699", "44700", "44697", "210", "44698"], "item_4_biblio_info_8": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2007-09-15", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "1-2", "bibliographicPageEnd": "239", "bibliographicPageStart": "236", "bibliographicVolumeNumber": "260", "bibliographic_titles": [{"bibliographic_title": "Journal of the Neurological Sciences"}]}]}, "item_4_description_21": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "A family with familial amyloid polyneuropathy (FAP) due to a transthyretin (TTR) Leu58Arg mutation was investigated clinicopathologically. The proband presented with sensorimotor-autonomic polyneuropathy and autopsy demonstrated massive amyloid deposition in the peripheral nerves and heart. However, the mother was characterized by carpal tunnel syndrome and ocular vitreous opacities. Thus, there was considerable phenotypic heterogeneity among family members despite the identical TTR genotype. © 2007 Elsevier B.V. All rights reserved.", "subitem_description_type": "Abstract"}]}, "item_4_description_5": {"attribute_name": "提供者所属", "attribute_value_mlt": [{"subitem_description": "金沢大学医学部附属病院神経内科", "subitem_description_type": "Other"}]}, "item_4_publisher_17": {"attribute_name": "出版者", "attribute_value_mlt": [{"subitem_publisher": "Elsevier"}]}, "item_4_relation_12": {"attribute_name": "DOI", "attribute_value_mlt": [{"subitem_relation_type": "isVersionOf", "subitem_relation_type_id": {"subitem_relation_type_id_text": "10.1016/j.jns.2007.03.021", "subitem_relation_type_select": "DOI"}}]}, "item_4_source_id_9": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "0022-510X", "subitem_source_identifier_type": "ISSN"}]}, "item_4_version_type_25": {"attribute_name": "著者版フラグ", "attribute_value_mlt": [{"subitem_version_resource": "http://purl.org/coar/version/c_ab4af688f83e57aa", "subitem_version_type": "AM"}]}, "item_creator": {"attribute_name": "著者", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Motozaki, Yuko"}], "nameIdentifiers": [{"nameIdentifier": "44696", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Sugiyama, Yu"}], "nameIdentifiers": [{"nameIdentifier": "44697", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Ishida, Chiho"}], "nameIdentifiers": [{"nameIdentifier": "44698", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Komai, Kiyonobu"}], "nameIdentifiers": [{"nameIdentifier": "44699", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Matsubara, Shiro"}], "nameIdentifiers": [{"nameIdentifier": "44700", "nameIdentifierScheme": "WEKO"}, {"nameIdentifier": "00143884", "nameIdentifierScheme": "e-Rad", "nameIdentifierURI": "https://kaken.nii.ac.jp/ja/search/?qm=00143884"}]}, {"creatorNames": [{"creatorName": "Yamada, Masahito"}], "nameIdentifiers": [{"nameIdentifier": "210", "nameIdentifierScheme": "WEKO"}, {"nameIdentifier": "80191336", "nameIdentifierScheme": "e-Rad", "nameIdentifierURI": "https://kaken.nii.ac.jp/ja/search/?qm=80191336"}, {"nameIdentifier": "80191336", "nameIdentifierScheme": "金沢大学研究者情報", "nameIdentifierURI": "http://ridb.kanazawa-u.ac.jp/public/detail.php?kaken=80191336"}, {"nameIdentifier": "80191336", "nameIdentifierScheme": "研究者番号", "nameIdentifierURI": "https://nrid.nii.ac.jp/nrid/1000080191336"}]}]}, "item_files": {"attribute_name": "ファイル情報", "attribute_type": "file", "attribute_value_mlt": [{"accessrole": "open_date", "date": [{"dateType": "Available", "dateValue": "2017-10-05"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "HO-PR-MOTOZAKI-Y-236.pdf", "filesize": [{"value": "257.6 kB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 257600.00000000003, "url": {"label": "HO-PR-MOTOZAKI-Y-236.pdf", "url": "https://kanazawa-u.repo.nii.ac.jp/record/26623/files/HO-PR-MOTOZAKI-Y-236.pdf"}, "version_id": "8977e151-2e3d-40e5-9a92-412fa501e9da"}]}, "item_keyword": {"attribute_name": "キーワード", "attribute_value_mlt": [{"subitem_subject": "Carpal tunnel syndrome", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Familial amyloid polyneuropathy", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Mutation", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Transthyretin", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Vitreous opacity", "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": "Phenotypic heterogeneity in a family with FAP due to a TTR Leu58Arg mutation: A clinicopathologic study", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "Phenotypic heterogeneity in a family with FAP due to a TTR Leu58Arg mutation: A clinicopathologic study"}]}, "item_type_id": "4", "owner": "3", "path": ["1763"], "permalink_uri": "http://hdl.handle.net/2297/7021", "pubdate": {"attribute_name": "公開日", "attribute_value": "2017-10-05"}, "publish_date": "2017-10-05", "publish_status": "0", "recid": "26623", "relation": {}, "relation_version_is_last": true, "title": ["Phenotypic heterogeneity in a family with FAP due to a TTR Leu58Arg mutation: A clinicopathologic study"], "weko_shared_id": 3}
Phenotypic heterogeneity in a family with FAP due to a TTR Leu58Arg mutation: A clinicopathologic study
http://hdl.handle.net/2297/7021
http://hdl.handle.net/2297/702182c048d6-50d6-407b-8e66-68b1f5c81262
名前 / ファイル | ライセンス | アクション |
---|---|---|
HO-PR-MOTOZAKI-Y-236.pdf (257.6 kB)
|
|
Item type | 学術雑誌論文 / Journal Article(1) | |||||
---|---|---|---|---|---|---|
公開日 | 2017-10-05 | |||||
タイトル | ||||||
タイトル | Phenotypic heterogeneity in a family with FAP due to a TTR Leu58Arg mutation: A clinicopathologic study | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
著者 |
Motozaki, Yuko
× Motozaki, Yuko× Sugiyama, Yu× Ishida, Chiho× Komai, Kiyonobu× Matsubara, Shiro× Yamada, Masahito |
|||||
提供者所属 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 金沢大学医学部附属病院神経内科 | |||||
書誌情報 |
Journal of the Neurological Sciences 巻 260, 号 1-2, p. 236-239, 発行日 2007-09-15 |
|||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0022-510X | |||||
DOI | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1016/j.jns.2007.03.021 | |||||
出版者 | ||||||
出版者 | Elsevier | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | A family with familial amyloid polyneuropathy (FAP) due to a transthyretin (TTR) Leu58Arg mutation was investigated clinicopathologically. The proband presented with sensorimotor-autonomic polyneuropathy and autopsy demonstrated massive amyloid deposition in the peripheral nerves and heart. However, the mother was characterized by carpal tunnel syndrome and ocular vitreous opacities. Thus, there was considerable phenotypic heterogeneity among family members despite the identical TTR genotype. © 2007 Elsevier B.V. All rights reserved. | |||||
著者版フラグ | ||||||
出版タイプ | AM | |||||
出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa |