{"id":901,"date":"2014-07-14T00:02:10","date_gmt":"2014-07-13T15:02:10","guid":{"rendered":"http:\/\/yuge-ent-clinic.com\/?page_id=901"},"modified":"2025-11-10T14:01:00","modified_gmt":"2025-11-10T05:01:00","slug":"medline1","status":"publish","type":"page","link":"http:\/\/yuge-ent-clinic.com\/?page_id=901","title":{"rendered":"Medline1"},"content":{"rendered":"

medline\u306b\u3066\u691c\u7d22<\/a><\/h4>\n

Sato M, Ogawa K, Saito H, Yamashita D, Yuge I<\/strong>, Masuda M, Okamoto Y, Kurita A.
\n [Evaluation of the quality of life in sudden deafness patients by HHIA (hearing Hatidicap Inventory) and questionnaire]
\n Nippon Jibiinkoka Gakkai Kaiho. 2005 Dec;108(12):1158-64. Japanese. <\/p>\n

Yuge I<\/strong>, Takumi Y, Koyabu K, Hashimoto S, Takashima S, Fukuyama T, Nikaido T, Usami S.
\n Transplanted human amniotic epithelial cells express connexin 26 and Na-K-adenosine triphosphatase in the inner ear.
\n Transplantation. 2004 May 15;77(9):1452-4. <\/p>\n

Usami S, Takahashi K, Yuge I<\/strong>, Ohtsuka A, Namba A, Abe S, Fransen E, Patthy L, Otting G, Van Camp G.
\n Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere’s disease.
\n Eur J Hum Genet. 2003 Oct;11(10):744-8. <\/p>\n

Imanishi Y, Nameki H, Isobe K, Kaneda T, Yamashita D, Yuge I<\/strong>, Okada W, Nameki I, Araki Y, Suzuki T.
\n Intramucosal PCO2 measurement as a new monitoring method of free jejunal transfer following pharyngo-laryngo-esophagectomy.
\n Plast Reconstr Surg. 2003 Oct;112(5):1247-56. <\/p>\n

Ohtsuka A, Yuge I<\/strong>, Kimura S, Namba A, Abe S, Van Laer L, Van Camp G, Usami S.
\n GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation.
\n Hum Genet. 2003 Apr;112(4):329-33. Epub 2003 Jan 31. <\/p>\n

Yuge I<\/strong>, Ohtsuka A, Matsunaga T, Usami S.
\n Identification of 605ins46, a novel GJB2 mutation in a Japanese family.
\n Auris Nasus Larynx. 2002 Oct;29(4):379-82. <\/p>\n

Usami S, Koda E, Tsukamoto K, Otsuka A, Yuge I<\/strong>, Asamura K, Abe S, Akita J, Namba A.
\n Molecular diagnosis of deafness: impact of gene identification.
\n Audiol Neurootol. 2002 May-Jun;7(3):185-90. <\/p>\n

<\/p>\n","protected":false},"excerpt":{"rendered":"

medline\u306b\u3066\u691c\u7d22 Sato M, Ogawa K, Saito H, Yamashita D, Yuge I, Masuda M, Okamoto Y, Kurita A. [Evaluation of the q […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"close","ping_status":"open","template":"","meta":{"footnotes":""},"_links":{"self":[{"href":"http:\/\/yuge-ent-clinic.com\/index.php?rest_route=\/wp\/v2\/pages\/901"}],"collection":[{"href":"http:\/\/yuge-ent-clinic.com\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/yuge-ent-clinic.com\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/yuge-ent-clinic.com\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/yuge-ent-clinic.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=901"}],"version-history":[{"count":3,"href":"http:\/\/yuge-ent-clinic.com\/index.php?rest_route=\/wp\/v2\/pages\/901\/revisions"}],"predecessor-version":[{"id":3920,"href":"http:\/\/yuge-ent-clinic.com\/index.php?rest_route=\/wp\/v2\/pages\/901\/revisions\/3920"}],"wp:attachment":[{"href":"http:\/\/yuge-ent-clinic.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=901"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}