Hisakuni Fukuoka

Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese

Hisakuni Fukuoka, Yukihiko Kanda, Shuji Ohta et al. · Journal of Human Genetics · 2007 · 81 citations

Life Sciences, Audiology, Genetics +13

Achievement of hearing preservation in the presence of an electrode covering the residual hearing region

Shin‐ichi Usami, Hideaki Moteki, Nobuyoshi Suzuki et al. · Acta Oto-Laryngologica · 2011 · 78 citations · Full text

Medicine, Otolaryngology, Surgery +17

Comparison of the diagnostic value of 3 T MRI after intratympanic injection of GBCA, electrocochleography, and the glycerol test in patients with Meniere's disease

Hisakuni Fukuoka, Yutaka Takumi, Keita Tsukada et al. · Acta Oto-Laryngologica · 2011 · 67 citations · Full text

Medicine, Otolaryngology, Radiology +13

Semi-quantitative evaluation of endolymphatic hydrops by bilateral intratympanic gadolinium-based contrast agent (GBCA) administration with MRI for Meniere's disease

Hisakuni Fukuoka, Keita Tsukada, Maiko Miyagawa et al. · Acta Oto-Laryngologica · 2010 · 41 citations

Medicine, Otolaryngology, Radiology +16

Endolymphatic hydrops and therapeutic effects are visualized in ‘atypical’ Meniere's disease

Maiko Miyagawa, Hisakuni Fukuoka, Keita Tsukada et al. · Acta Oto-Laryngologica · 2009 · 36 citations

Medicine, Otolaryngology, Radiology +17