{"id":4231,"date":"2023-05-11T19:27:08","date_gmt":"2023-05-11T10:27:08","guid":{"rendered":"https:\/\/www.kyorin-u.ac.jp\/univ\/faculty\/medicine\/?p=4231"},"modified":"2023-05-11T19:28:20","modified_gmt":"2023-05-11T10:28:20","slug":"%e5%b0%8f%e5%85%90%e7%a7%91%e5%ad%a6%e6%95%99%e5%ae%a4-%e6%9c%a8%e5%86%85-%e5%96%84%e5%a4%aa%e9%83%8e-%e5%8a%a9%e6%95%99%e3%81%aejcem-case-reports%e3%81%ab%e6%8e%b2%e8%bc%89%e3%81%95%e3%82%8c%e3%81%9f","status":"publish","type":"post","link":"https:\/\/www.kyorin-u.ac.jp\/univ\/faculty\/medicine\/archive\/4231\/","title":{"rendered":"JCEM Case Reports\u306b\u63b2\u8f09\u3055\u308c\u305f\u8ad6\u6587\u304cFeatured Article\u306b\u9078\u51fa – \u5c0f\u5150\u79d1\u5b66\u6559\u5ba4 \u6728\u5185 \u5584\u592a\u90ce \u52a9\u6559"},"content":{"rendered":"

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\u63b2\u8f09\u8ad6\u6587<\/h5>\r\n\r\n\r\n \r\n \r\n \r\n \r\n
\u767a\u8868\u96d1\u8a8c\uff1a<\/td>JCEM Case Reports, Volume 1, Issue 2, March 2023\u3000(Published: 24 February 2023).<\/td>\r\n <\/tr>\r\n
\u8ad6\u6587\u30bf\u30a4\u30c8\u30eb\uff1a<\/td>Bartter Syndrome Type 1 Due to Novel SLC12A1 Mutations Associated With Pseudohypoparathyroidism Type II<\/a><\/td>\r\n <\/tr>\r\n
\u7b46\u3000\u8005\uff1a<\/td>Zentaro Kiuchi1<\/sup>, Kandai Nozu2<\/sup>, Kunimasa Yan1,3<\/sup>, and Harald J\u00fcppner4,5<\/sup>
\r\n(1.Department of Pediatrics, Kyorin University School of Medicine, Mitaka, Tokyo, Japan, 2.Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan, 3.Department of Pediatrics, Kosei Hospital, Suginami, Tokyo, Japan, 4.Endocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA, 5.Pediatric Nephrology Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA)<\/td>\r\n <\/tr>\r\n
DOI:<\/td> 10.1210\/jcemcr\/luad019<\/td>\r\n <\/tr>\r\n<\/table>\r\n","protected":false},"excerpt":{"rendered":"

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