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Audiology & Neuro-Otology|April 1, 2015
Vestibular functions of hereditary hearing loss patients with GJB2 mutationsKeita Tsukada, Hisakuni Fukuoka, Shin-Ichi Usami
Journal of Human Genetics|May 12, 2007
Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in JapaneseHisakuni Fukuoka, Yukihiko Kanda, Shuji Ohta, et al.
Frontiers in Allergy|May 25, 2026
Interpretable machine learning classification of cedar and cypress pollen on routine Durham slides for environmental exposure assessmentNobuyoshi Suzuki, Kenjiro Sugiyama, Katsuhiko Kobayashi, et al.
Acta Oto-Laryngologica|September 7, 2013
Effects of EAS cochlear implantation surgery on vestibular functionKeita Tsukada, Hideaki Moteki, Hisakuni Fukuoka, et al.
Auris, Nasus, Larynx|May 27, 2005
Mutation analysis of COL9A3, a gene highly expressed in the cochlea, in hearing loss patientsKenji Asamura, Satoko Abe, Hisakuni Fukuoka, et al.
Acta Oto-Laryngologica|March 28, 2008
The responsible genes in Japanese deafness patients and clinical application using Invader assayShin-Ichi Usami, Michio Wagatsuma, Hisakuni Fukuoka, et al.
Plos One|December 6, 2018
Bilateral delayed endolymphatic hydrops evaluated by bilateral intratympanic injection of gadodiamide with 3T-MRIYoh-Ichiro Iwasa, Keita Tsukada, Masafumi Kobayashi, et al.
Acta Oto-Laryngologica|October 30, 2009
Endolymphatic hydrops and therapeutic effects are visualized in 'atypical' Meniere's diseaseMaiko Miyagawa, Hisakuni Fukuoka, Keita Tsukada, et al.
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