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Plos Genetics|April 16, 2020
Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humansHideki Mutai, Koichiro Wasano, Yukihide Momozawa, et al.Scientific Reports|April 22, 2023
Correlation between genotype and phenotype with special attention to hearing in 14 Japanese cases of NF2-related schwannomatosisNaoki Oishi, Masaru Noguchi, Masato Fujioka, et al.Acta Oto-Laryngologica|January 17, 2013
A psychometric validation of the Japanese versions of new questionnaires on tinnitus (THI-12, TRS, TRSw, TSS, and TSSw)Koichiro Wasano, Sho Kanzaki, Tetsushi Sakashita, et al.Journal of Medical Case Reports|April 8, 2026
Recurrent laryngeal nerve schwannoma adjacent to the thyroid: a case reportMayu Yamauchi, Akihiro Sakai, Hiroaki Iijima, et al.Auris, Nasus, Larynx|June 23, 2026
Tetanus mimicking post-radiotherapy dysphagia in a head and neck cancer survivor:A case report with institutional reviewHiroaki Iijima, Akihiro Sakai, Mayu Yamauchi, et al.Laryngoscope Investigative Otolaryngology|September 29, 2025
Comprehensive Genetic Analysis of <i>NF2</i> in Sporadic Vestibular SchwannomaTakeshi Wakabayashi, Koichiro Wasano, Kohei Nakamura, et al.Japanese Journal of Clinical Oncology|August 29, 2024
Frequency of use and cost in Japan of first-line palliative chemotherapies for recurrent or metastatic squamous cell carcinoma of the head and neckKazuki Yokoyama, Koichiro Wasano, Keita Sasaki, et al.Cancers|August 27, 2021
Prevalence of Germline Variants in a Large Cohort of Japanese Patients with Pheochromocytoma and/or ParagangliomaMasato Yonamine, Koichiro Wasano, Yuichi Aita, et al.Human Genetics|January 4, 2025
Genetic landscape in undiagnosed patients with syndromic hearing loss revealed by whole exome sequencing and phenotype similarity searchHideki Mutai, Fuyuki Miya, Kiyomitsu Nara, et al.BMC Medicine|April 16, 2026
Development of a novel prognostic assessment tool for recurrent respiratory papillomatosisSatoshi Yamada, Taro Ikegami, Takahiro Fukuhara, et al.Pageof 7