{"created":"2023-06-20T17:00:41.233955+00:00","id":20179,"links":{},"metadata":{"_buckets":{"deposit":"a3ef4451-3409-4b99-ad3b-5de64a16915b"},"_deposit":{"created_by":3,"id":"20179","owners":[3],"pid":{"revision_id":0,"type":"depid","value":"20179"},"status":"published"},"_oai":{"id":"oai:twinkle.repo.nii.ac.jp:00020179","sets":["140:1307:1308:2014:2022"]},"author_link":["294331","294325","294330","294327","294326","294328","294332","294329"],"item_10001_alternative_title_1":{"attribute_name":"別タイトル","attribute_value_mlt":[{"subitem_alternative_title":"A Case Report of Bartter's Syndrome with Severe Growth Retardation and Abnormal Serum Electrolites(Papers for cerebrating the Forty Aniversary of the Department of Pediatrics, Tokyo Women's Medical University Center East)"}]},"item_10001_biblio_info_7":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2007-05-31","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"Extra","bibliographicPageEnd":"E91","bibliographicPageStart":"E85","bibliographicVolumeNumber":"77","bibliographic_titles":[{"bibliographic_title":"東京女子医科大学雑誌"}]}]},"item_10001_creator_2":{"attribute_name":"著者名","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"溝口, 由美子"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"鈴木, 里香"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"鈴木, 恵子"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"杉原, 茂孝"}],"nameIdentifiers":[{}]}]},"item_10001_date_25":{"attribute_name":"受付日付","attribute_value_mlt":[{"subitem_date_issued_datetime":"2010-08-10","subitem_date_issued_type":"Created"}]},"item_10001_description_34":{"attribute_name":"注記","attribute_value_mlt":[{"subitem_description":"東京女子医科大学東医療センター小児科開局40周年記念論文集","subitem_description_type":"Other"}]},"item_10001_description_5":{"attribute_name":"抄録","attribute_value_mlt":[{"subitem_description":"Bartter's syndrome is a rare inherited renal tubular disorder. We experienced an 8-month old male patient admitted to our ward with hepatitis. His growth was severely retarded, and he had abnormalities of serum electrolytes including hyponatremia, hypokalemia, and hypochloremia with metabolic alkalosis. He needed continuous intravenous infusion and electrolyte supplementation. Further, his plasma renin and aldosterone concentrations were remarkably elevated. Because of his normal blood pressure, normal serum magnesium and hypercalciuria, we diagnosed him as having Bartter's syndrome. Gene analysis revealed type III Bartter's syndrome.","subitem_description_type":"Abstract"}]},"item_10001_full_name_3":{"attribute_name":"著者別名","attribute_value_mlt":[{"nameIdentifiers":[{"nameIdentifier":"294329","nameIdentifierScheme":"WEKO"}],"names":[{"name":"MIZOGUCHI, Yumiko"}]},{"nameIdentifiers":[{"nameIdentifier":"294330","nameIdentifierScheme":"WEKO"}],"names":[{"name":"SUZUKI, Rika"}]},{"nameIdentifiers":[{"nameIdentifier":"294331","nameIdentifierScheme":"WEKO"}],"names":[{"name":"SUZUKI, Keiko"}]},{"nameIdentifiers":[{"nameIdentifier":"294332","nameIdentifierScheme":"WEKO"}],"names":[{"name":"SUGIHARA, Shigetaka"}]}]},"item_10001_publisher_8":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"東京女子医科大学学会"}]},"item_10001_source_id_11":{"attribute_name":"NCID","attribute_value_mlt":[{"subitem_source_identifier":"AN00161368","subitem_source_identifier_type":"NCID"}]},"item_10001_source_id_9":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"0040-9022","subitem_source_identifier_type":"ISSN"}]},"item_10001_subject_47":{"attribute_name":"著者キーワード","attribute_value_mlt":[{"subitem_subject":"Bartter's syndrome","subitem_subject_scheme":"Other"},{"subitem_subject":"growth retardation","subitem_subject_scheme":"Other"},{"subitem_subject":"hypokalemia","subitem_subject_scheme":"Other"},{"subitem_subject":"metabolic alkalosis","subitem_subject_scheme":"Other"},{"subitem_subject":"elevation of plasma renin and aldosterone concentration","subitem_subject_scheme":"Other"}]},"item_10001_text_35":{"attribute_name":"著者所属","attribute_value_mlt":[{"subitem_text_value":"東京女子医科大学東医療センター小児科:(現)光ヶ丘スペルマン病院小児科"},{"subitem_text_value":"東京女子医科大学東医療センター小児科:(現)光ヶ丘スペルマン病院小児科"},{"subitem_text_value":"東京女子医科大学東医療センター小児科:(現)光ヶ丘スペルマン病院小児科"},{"subitem_text_value":"東京女子医科大学東医療センター小児科:(現)光ヶ丘スペルマン病院小児科"}]},"item_10001_version_type_20":{"attribute_name":"著者版フラグ","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_970fb48d4fbd8a85","subitem_version_type":"VoR"}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2017-08-22"}],"displaytype":"detail","filename":"KJ00006017919.pdf","filesize":[{"value":"978.6 kB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"KJ00006017919.pdf","url":"https://twinkle.repo.nii.ac.jp/record/20179/files/KJ00006017919.pdf"},"version_id":"1b22550e-9ffc-4d22-b7da-54c15567b490"}]},"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":"journal article","resourceuri":"http://purl.org/coar/resource_type/c_6501"}]},"item_title":"著明な発育障害と血清電解質異常で発見されたBartter症候群の1例(東京女子医科大学東医療センター小児科開局40周年記念論文集)","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"著明な発育障害と血清電解質異常で発見されたBartter症候群の1例(東京女子医科大学東医療センター小児科開局40周年記念論文集)"}]},"item_type_id":"10001","owner":"3","path":["2022"],"pubdate":{"attribute_name":"公開日","attribute_value":"2010-08-10"},"publish_date":"2010-08-10","publish_status":"0","recid":"20179","relation_version_is_last":true,"title":["著明な発育障害と血清電解質異常で発見されたBartter症候群の1例(東京女子医科大学東医療センター小児科開局40周年記念論文集)"],"weko_creator_id":"3","weko_shared_id":3},"updated":"2023-06-20T19:58:06.689248+00:00"}