教室案内

論文実績

2021

  • Keita Tsukada, Shin-ichi Usami. Vestibular preservation after cochlear implantation using the round window approach. Front Neurol. 12: 656592. 2021
  • Hidekane Yoshimura, Masahiro Takahashi, Satoshi Iwasaki, Jun Shinagawa, Ikkei Takashimizu, Fumio Nagai, Takatoshi Yotsuyanagi, Shin-ichi Usami. Vibrant soundbridge implantation prior to auricular reconstruction with unilateral microtia‐atresia. Clin Case Rep. 9(8): e04408. 2021
  • Hidekane Yoshimura, Shin-ya Nishio, Shin-ichi Usami. Milestones toward cochlear gene therapy for patients with hereditary hearing loss. Laryngoscope Investig Otolaryngol. 6(5): 958-967. 2021
  • Keita Tsukada, Shin-ichi Usami. Vestibular nerve deficiency and vestibular function in children with unilateral hearing loss caused by cochlear nerve deficiency. Acta Otolaryngol. 141(9): 835-840. 2021
  • Hidekane Yoshimura, Shin-ya Nishio, Yuichi Isaka, Toru Kurokawa, Shin-ichi Usami, Interactable Hearing Disorder Consortium. A nationwide epidemiologic, clinical, genetic study of Usher syndrome in Japan. Acta Otolaryngol. 141(9): 841-846. 2021
  • Mariko Kasuga, Hidekane Yoshimura, Jun Shinagawa, Shin-ya Nishio, Yutaka Takumi, Shin-ichi Usami. Frequency and natural course of congenital cytomegalovirus-associated hearing loss in children. Acta Otolaryngol. 141(12):1038-1043. 2021
  • Yoh-ichiro Iwasa, Shin-ya Nishio, Hidekane Yoshimura, Akiko Sugaya, Yuko Kataoka, Yukihide Maeda, Yukihiko Kanda, Kyoko Nagai, Yasushi Naito, Hiroshi Yamazaki, Tetsuo Ikezono, Han Matsuda, Masako Nakai, Risa Tona, Yuika Sakurai, Remi Motegi, Hidehiko Takeda, Marina Kobayashi, Chiharu Kihara, Takashi Ishino, Shin-ya Morita, Satoshi Iwasaki, Masahiro Takahashi, Sakiko Furutate, Shin-ichiro Oka, Toshinori Kubota, Yasuhiro Arai, Yumiko Kobayashi, Daisuke Kikuchi, Tomoko Shintani, Noriko Ogasawara, Yohei Honkura, Shuji Izumi, Misako Hyogo, Yuzuru Ninoyu, Mayumi Suematsu, Jun Nakayama, Nana Tsuchihashi, Mayuri Okami, Hideaki Sakata, Hiroshi Yoshihashi, Taisuke Kobayashi, Kozo Kumakawa, Tadao Yoshida, Tomoko Esaki, and Shin-ichi Usami. Detailed clinical features and genotype–phenotype correlation in an OTOF-related hearing loss cohort in Japan. Hum Genet. 141(3-4): 865-875. 2022
  • Ken Hiramatsu, Shin-ya Nishio, Shin-ichiro Kitajiri, Tomohiro Kitano, Hideaki Moteki, Shin-ichi Usami, On behalf of the deafness gene study consortium. Prevalence and clinical characteristics of hearing loss caused by MYH14 variants. Genes. 12(10):1623. 2021
  • Kazuki Matsuura, Hidekane Yoshimura, Jun Shinagawa, Masahiro Kurozumi, Yutaka Takumi. Audiological features in 63 patients with cochlear nerve deficiency. Otol Neurotol. 43(1):23-28. 2022
  • Yoh-ichiro Iwasa, Yoh Yokota, Ryosuke Kitoh, Kentaro Mori, Keita Tsukada, Nodoka Sekiguchi, Toshirou Fukushima, Takashi Kobayashi, Shintaro Kanda, Yutaka Takumi, Tomonobu Koizumi. Factors affecting nivolumab therapy outcome in patients with head and neck cancer: A single-center analysis. Oncology. 100(4): 203-211. 2022
  • Hiroshi Yamamoto, Masamichi Komatsu, Kei Sonehara, Yuichi Ikuyama, Kazuhisa Urushihata, Kazunari Tateishi, Yoshiaki Kitaguchi, Atsuhito Ushiki, Shiho Asaka, Takeshi Uehara, Satoshi Kawakami, Kentaro Mori, Kazutoshi Hamanaka, Kenichi Nishie, Akira Hebisawa, Masayuki Hanaoka. Usual interstitial pneumonia pattern interstitial lung disease developed in a patient with IgG4-related chronic sclerosing sialadenitis: a case report. Intern Med. 8937-21. 2022
  • Klomp A, Omichi R, Iwasa Y, Smith RJ, Usachev YM, Russo AF, et al. The voltage-gated Ca2+ channel subunit α2δ-4 regulates locomotor behavior and sensorimotor gating in mice. PLoS One. 17(3):1–14. 2022
  • Ryosuke Kitoh, Shin-ya Nishio, Shin-ichi Usami. Speech perception in noise in patients with idiopathic sudden hearing loss. Acta Otolaryngol. 142(3-4):302-307. 2022
  • 工 穣
    【チャートでみる耳鼻咽喉科診療】症状から診断へ 耳科領域 新生児聴覚スクリーニング
    JOHNS 37(9): 931-935. 2021
  • 工 穣
    【よくわかる医療文書の書き方】指定難病医療費助成制度と文書作成 耳科領域
    JOHNS 37(10): 1328-1336. 2021
  • 平松 憲、岩佐陽一郎、鬼頭良輔、工 穣
    セツキシマブ併用放射線治療中にニューモシスチス肺炎を発症し、診断に苦慮した1例
    信州医学雑誌 69(5): 245-251. 2021
  • 石川浩太郎、吉村豪兼、西尾信哉、宇佐美真一
    【次世代シーケンサー時代の難聴遺伝子診断と臨床応用】アッシャー症候群
    Audiology Japan 31(2): 142-147. 2021
  • 工 穣
    【必読!メニエール病の新分類とその周辺疾患】メニエール病の周辺疾患の診断・治療 めまいを伴う特発性感音難聴(DFNA9,DFNA6/14/38)
    耳鼻咽喉科・頭頸部外科 93(12): 1014-1019. 2021
  • 内田育恵、大石直樹、工 穣、中川尚志、西崎和則、白馬伸洋、村上信五
    プロダクティブ・エイジング(生産的高齢化)社会の実現に向けた難聴者への補聴器導入補聴器を始めたシニアの変化
    日本耳鼻咽喉科頭頸部外科学会会報124(11): 1452-1456. 2021
  • 高橋優宏、岩崎 聡、吉村豪兼、古館佐起子、岡晋一郎、西尾信哉、宇佐美真一
    一側伝音・混合性難聴に対する人工中耳(Vibrant Soundbridge:VSB)装用効果の検討
    Otology Japan 32(1): 129-135. 2022
  • 岩佐陽一郎、鬼頭良輔、宇佐美真一
    化学放射線療法後に咽頭粘膜壊死を生じた中咽頭癌の1例
    頭頸部外科 31(3): 267-272. 2022

2020

  • Shinagawa J, Moteki H, Nishio SY, Ohyama K, Otsuki K, Iwasaki S, Masuda S, Oshikawa C, Ohta Y, Arai Y, Takahashi M, Sakuma N, Abe S, Sakurai Y, Sakaguchi H, Ishino T, Uehara N, Usami SI. Prevalence and clinical features of hearing loss caused by EYA4 variants. Sci Rep. 2020 Feb 27;10(1):3662.
  • Usami SI, Nishio SY, Moteki H, Miyagawa M, Yoshimura H. Cochlear Implantation From the Perspective of Genetic Background. Anat Rec (Hoboken). 2020 Mar;303(3):563-593.
  • Kitoh R, Nishio SY, Usami SI. Treatment algorithm for idiopathic sudden sensorineural hearing loss based on epidemiologic surveys of a large Japanese cohort. Acta Otolaryngol. 2020 Jan;140(1):32-39.
  • Shinagawa J, Moteki H, Nishio SY, Noguchi Y, Usami SI. Haplotype Analysis of GJB2Mutations: Founder Effect or Mutational Hot Spot? Genes (Basel). 2020 Feb 27;11(3):250.
  • Moteki H, Kitoh R, Usami SI. The availability of an adhesive bone conduction hearing device: a preliminary report of a single-center experience. Acta Otolaryngol. 2020 Apr;140(4):319-326.
  • Oka SI, Day TF, Nishio SY, Moteki H, Miyagawa M, Morita S, Izumi S, Ikezono T, Abe S, Nakayama J, Hyogo M, Okamoto N, Uehara N, Oshikawa C, Kitajiri SI, Usami SI. Clinical Characteristics and In Vitro Analysis of MYO6Variants Causing Late-Onset Progressive Hearing Loss. Genes (Basel). 2020 Mar 4;11(3):273.
  • Yoshimura H, Moteki H, Nishio SY, Miyajima H, Miyagawa M, Usami SI. Genetic testing has the potential to impact hearing preservation following cochlear implantation. Acta Otolaryngol. 2020 Jun;140(6):438-444.
  • Fujioka M, Akiyama T, Hosoya M, Kikuchi K, Fujiki Y, Saito Y, Yoshihama K, Ozawa H, Tsukada K, Nishio SY, Usami SI, Matsunaga T, Hasegawa T, Sato Y, Ogawa K. A phase I/IIa double blind single institute trial of low dose sirolimus for Pendred syndrome/DFNB4. Medicine (Baltimore). 2020 May;99(19):e19763.
  • Walls WD, Moteki H, Thomas TR, Nishio SY, Yoshimura H, Iwasa Y, Frees KL, Nishimura CJ, Azaiez H, Booth KT, Marini RJ, Kolbe DL, Weaver AM, Schaefer AM, Wang K, Braun TA, Usami SI, Barr-Gillespie PG, Richardson GP, Smith RJ, Casavant TL. A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations. Hum Genet. 2020 Oct;139(10):1315-1323.
  • Miyajima H, Moteki H, Day T, Nishio SY, Murata T, Ikezono T, Takeda H, Abe S, Iwasaki S, Takahashi M, Naito Y, Yamazaki H, Kanda Y, Kitajiri SI, Usami SI. Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss. Sci Rep. 2020 Apr 27;10(1):7056.
  • Yoshimura H, Moteki H, Nishio SY, Usami SI. Electric-acoustic stimulation with longer electrodes for potential deterioration in low-frequency hearing. Acta Otolaryngol. 2020 Aug;140(8):632-638.
  • Tsukada K, Usami SI. Detailed MR imaging assessment of endolymphatic hydrops in patients with SLC26A4 mutations. Auris Nasus Larynx. 2020 Dec;47(6):958-964.
  • Omichi R, Yoshimura H, Shibata SB, Vandenberghe LH, Smith RJH. Hair Cell Transduction Efficiency of Single- and Dual-AAV Serotypes in Adult Murine Cochleae. Mol Ther Methods Clin Dev. 2020 May 13;17:1167-1177.
  • Shibata SB, West MB, Du X, Iwasa Y, Raphael Y, Kopke RD. Gene therapy for hair cell regeneration: Review and new data. Hear Res. 2020 Sep 1;394:107981.

2019

  • G¨urkov R, Barath K, Foer B, Fukushima M, Gluth M, Hornibrook J, Perez-Fernandez N, Pyykk¨o I, Sone M, Usami SI, Wamg W, Zou J, Naganawa S.
    A plea for systematic literature analysisand conclusive study design, comment on: “Systematic review of magnetic resonanceimaging for diagnosis of Meniere disease” J Vestib Res. 2019
  • Sugiyama K, Moteki H, Kitajiri SI, Kitano T, Nishio SY, Yamaguchi T, Wakui K, Abe S, Ozaki A, Motegi R, Matsui H, Teraoka M, Kobayashi Y, Kosho T, Usami SI.
    Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss. Genes. 10(9)E715 2019
  • Kitano T, Kitajiri SI, Nishio SY, Usami SI.
    Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant. Int J Mol Sci. 20:4579 2019
  • Ideura M, Nishio SY, Moteki H, Takumi Y, Miyagawa M, Sato T, Kobayashi Y, Ohyama K, Oda K, Matsui T, Ito T, Suzumura H, Nagai K, Izumi S, Nisiyama N, Komori M, Kumakawa K, Takeda H, Kishimoto Y, Iwasaki S, Furutate S, Ishikawa K, Fujioka M, Nakanishi H, Nakayama J, Horie R, Ohta Y, Naito Y, Kakudo M, Sakaguchi H, Kataoka Y, Sugawara K, Hato N, Nakagawa T, Tsuchihashi N, Kanda Y, Kihara CH, Tono T, Miyanohara I, Ganaha A, Usami SI.
    Comprehensive analysis of syndromic hearing loss patients in Japan. Sci Rep. 9 11976 2019
  • Yoshimura H, Shibata SB, Ranum PT, Moteki H, Smith RJH.
    Targeted Allele Suppression Prevents Progressive Hearing Loss in the Mature Murine Model of Human TMC1 Deafness. Mol Ther. 27(3) 681-690 2019
  • Kitoh R, Mori K, Usami SI.
    Investigation of Recurrent Cases of Head and Neck Cancer after Initial Treatment. Int J Pract Otolaryngol 2 e11-e17 2019
  • Iwasa Y, Nishio SY, Sugaya A, Kataoka Y, Kanda Y, Taniguchi M, Nagai K, Naito Y, Ikezono T, Horie R, Sakurai Y, Matsuoka R, Takeda H, Abe S, Kihara C, Ishino T, Morita S, Iwasaki S, Takahashi M, Ito T, Arai Y,Usami SI.
    OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients. PLoS ONE 14(5) e0215932 2019
  • Yokota Y, Moteki H, Nishio SY, Yamaguchi T, Wakui K, Kobayashi Y, Ohyama K, Miyazaki H, Matsuoka R, Abe S, Kumakawa K, Takahashi M, Sakaguchi H, Uehara N, Ishino T, Kosho T, Fukushima Y, Usami SI.
    Frequency and clinical featuresof hearing loss caused by STRC deletions. Sci Rep. 9 4408 2019
  • Moteki H, Nishio SY, Miyagawa M, Tsukada K, Noguchi Y, Usami SI.
    Feasibility of hearing preservation for residual hearing with longer cochlear implant electrodes. Acta Otolaryngol 31: 1084-1089 2019
  • DiStefano MT, Hemphill SE, Oza AM, Siegert RK, Grant AR, Hughes MY, Cushman BJ, Azaiez H, Booth KT, Chapin A, Duzkale H, Matsunaga T, Shen J, Zhang W, Kenna M, Schimmenti LA, Tekin M, Rehm HL, Tayoun ANA, Amr SS; ClinGen Hearing Loss Clinical Domain Working Group. ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs. Genet Med. 2019 Oct;21(10):2239-2247.
  • Katsuno T, Belyantseva IA, Cartagena-Rivera AX, Ohta K, Crump SM, Petralia RS, Ono K, Tona R, Imtiaz A, Rehman A, Kiyonari H, Kaneko M, Wang YX, Abe T, Ikeya M, Fenollar-Ferrer C, Riordan GP, Wilson EA, Fitzgerald TS, Segawa K, Omori K, Ito J, Frolenkov GI, Friedman TB, Kitajiri SI. TRIOBP-5 sculpts stereocilia rootlets and stiffens supporting cells enabling hearing. JCI Insight. 2019 Jun 20;4(12):e128561.
  • Yasukawa R, Moteki H, Nishio SY, Ishikawa K, Abe S, Honkura Y, Hyogo M, Mihashi R, Ikezono T, Shintani T, Ogasawara N, Shirai K, Yoshihashi H, Ishino T, Otsuki K, Ito T, Sugahara K, Usami SI. The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss. Genes (Basel). 2019 Sep 24;10(10):744.
  • Maekawa K, Nishio SY, Abe S, Goto SI, Honkura Y, Iwasaki S, Kanda Y, Kobayashi Y, Oka SI, Okami M, Oshikawa C, Sakuma N, Sano H, Shirakura M, Uehara N, Usami SI. Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient Cohort. Genes (Basel). 2019 Sep 23;10(10):735.
  • Kitoh R, Nishio SY, Usami SI. Treatment algorithm for idiopathic sudden sensorineural hearing loss based on epidemiologic surveys of a large Japanese cohort. Acta Otolaryngol. 2020 Jan;140(1):32-39.