Isamu Yuge

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

Akihiro Ohtsuka, Isamu Yuge, Shinobu Kimura et al. · Human Genetics · 2003 · 155 citations

Mendelian Disorder, Genetic Disorder, Frequent Founder Mutation +9

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

Shin‐ichi Usami, Kentaro Takahashi, Isamu Yuge et al. · European Journal of Human Genetics · 2003 · 94 citations

Mendelian Disorder, Vestibular System, Ophthalmology +9

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

Isamu Yuge, Yutaka Takumi, Kuni Koyabu et al. · Transplantation · 2004 · 36 citations

Regenerative Medicine, Signal Transduction, Cell Signaling +13

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

Naoki Oishi, Hiroyuki Yamada, Sho Kanzaki et al. · Acta Oto-Laryngologica · 2017 · 27 citations

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

Yorihisa Imanishi, Hideo Nameki, Kiyoshi Isobe et al. · Plastic & Reconstructive Surgery · 2003 · 12 citations

Carbon Dioxide, Gastroenterology, New Monitoring Method +19