Isamu Yuge

发表

Molecular Diagnosis of Deafness: Impact of Gene Identification

S. Usami, S. Abe, Koji Tsukamoto, 2002, Audiology and Neurotology.

Early-phase outcome of Tinnitus Retraining Therapy and comparison of sound therapy measures

K. Ogawa, S. Shinden, Yasuhide Okamoto, 2006 .

TRANSPLANTED HUMAN AMNIOTIC EPITHELIAL CELLS EXPRESS CONNEXIN 26 AND NA-K-ADENOSINE TRIPHOSPHATASE IN THE INNER EAR

T. Nikaido, S. Takashima, Y. Takumi, 2004, Transplantation.

GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation

G. Camp, S. Usami, S. Abe, 2003, Human Genetics.

Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease

G. Otting, E. Fransen, L. Patthy, 2003, European Journal of Human Genetics.

Treatment of glomus jugulare tumor with catecholamine secretion: A case report

H. Nameki, Y. Imanishi, Yasuhide Okamoto, 2001 .

Intramucosal PCO2 Measurement as a New Monitoring Method of Free Jejunal Transfer following Pharyngo-laryngo-esophagectomy

K. Isobe, H. Nameki, Y. Imanishi, 2003, Plastic and reconstructive surgery.

Assessment of hyperacusis with a newly produced Japanese version of the Khalfa hyperacusis questionnaire

Hiroyuki Yamada, Naoki Oishi, K. Ogawa, 2017, Acta oto-laryngologica.

Identification of 605ins46, a novel GJB2 mutation in a Japanese family.

T. Matsunaga, S. Usami, Isamu Yuge, 2002, Auris, nasus, larynx.