論文 Development and validation of an iPad-based Japanese language monosyllable speech perception test (iCI2004 monosyllable) Acta Otolaryngol,141(3):267-272 2021(Mar.) Author:Nishio SY, Tono T, Iwaki T, Moteki H, Suzuki K, Tsushima Y, Kashio A, Akamatsu Y, Sato H, Yaegashi K, Takeda H, Kumagai F, Nakashima T, Matsuda Y, Hato N, Dairoku T, Shiroma M, Kawai R, Usami SI.
Prevalence and Clinical Characteristics of Hearing Loss Caused by MYH14 Variants. Genes(Basel).,12(10):1623 2021 Author:Hiramatsu K, Nishio SY, Kitajiri SI, Kitano T, Moteki H, Usami SI, On Behalf Of The Deafness Gene Study Consortium.
Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in Japan Hum Genome Var,7:27 2020(Aug.) Author:Maeda Y, Sasaki A, Kasai S, Goto S, Nishio SY, Sawada K, Tokuda I, Itoh K, Usami SI, Matsubara A.
Electric-acoustic stimulation with longer electrodes for potential deterioration in low-frequency hearing Acta Otolaryngol,140(8):632-638 2020(Jul.) Author:Yoshimura H, Moteki H, Nishio SY, Usami SI.
Genetic testing has the potential to impact hearing preservation following cochlear implantation Acta Otolaryngol,140(6):438-444 2020(May) Author:Yoshimura H, Moteki H, Nishio SY, Miyajima H, Miyagawa M, Usami SI.
Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss Sci Rep,10(1):7056 2020(Apr.) Author: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.
Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-Onset Progressive Hearing Loss Genes (Basel),11(3):273 2020(Mar.) Author: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.
The availability of an adhesive bone conduction hearing device: a preliminary report of a single-center experience Acta Otolaryngol,140(4):319-326 2020(Mar.) Author:Moteki H, Kitoh R, Usami SI.
Haplotype Analysis of GJB2 Mutations: Founder Effect or Mutational Hot Spot? Genes (Basel),11(3):250 2020(Feb.) Author:Shinagawa J, Moteki H, Nishio SY, Noguchi Y, Usami SI.
Cochlear Implantation From the Perspective of Genetic Background Anat Rec (Hoboken),303(3):563-593 2020(Feb.) Author:Usami SI, Nishio SY, Moteki H, Miyagawa M, Yoshimura H.
Prevalence and clinical features of hearing loss caused by EYA4 variants Sci Rep,10(1):3662 2020(Jan.) Author: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.
The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss. ,10:744 2019 Author: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, ItoT, Sugahara K, Usami SI.
Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss. Genes.,10:715 2019 Author: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.
Comprehensive analysis of syndromic hearing loss patients in Japan. Sci Rep.,9:11976 2019 Author: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.
Frequency and clinical featuresof hearing loss caused by STRC deletions. Sci Rep.,9:4408 2019 Author: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.
Targeted Allele Suppression Prevents Progressive Hearing Loss in the Mature Murine Model of Human TMC1 Deafness. Mol Ther.,27(3):681-691 2019 Author:Yoshimura H, Shibata SB, Ranum PT, Moteki H, Smith RJH.
Feasibility of hearing preservation for residual hearing with longer cochlear implant electrodes. Acta Otolaryngol,138(12):1080-1085 2019 Author:Moteki H, Nishio SY, Miyagawa M, Tsukada K, Noguchi Y, Usami SI.
Long-term results of hearing preservation cochlear implant surgery in patients with residual low frequency hearing. Acta Otolaryngol,137(5):516-521 2017(May) Author:Moteki H, Nishio SY, Miyagawa M, Tsukada K, Iwasaki S, Usami SI.
POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss. PLoS One,12(5):e0177636 2017(May) Author:Kitano T, Miyagawa M, Nishio SY, Moteki H, Oda K, Ohyama K, Miyazaki H, Hidaka H, Nakamura KI, Murata T, Matsuoka R, Ohta Y, Nishiyama N, Kumakawa K, Furutate S, Iwasaki S, Yamada T, Ohta Y, Uehara N, Noguchi Y, Usami SI.
Self-assessment of Allergic Rhinitis and Asthma (SACRA) Questionnaire-based Allergic Rhinitis Treatment Improves Asthma Control in Asthmatic Patients with Allergic Rhinitis. Intern Med,56(1):31-39 2017 Author:Yasuo M, Kitaguchi Y, Komatsu Y, Hama M, Koizumi T, Agatsuma T, Ichiyama T, Kato A, Moteki H, Hanaoka M.
Etiology of single-sided deafness and asymmetrical hearing loss. Acta Otolaryngol,137(sup565):S2-S7 2017 Author:Usami SI, Kitoh R, Moteki H, Nishio SY, Kitano T, Kobayashi M, Shinagawa J, Yokota Y, Sugiyama K, Watanabe K.
Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic Hybridization. Ann Otol Rhinol Laryngol,125(11):918-923 2016(Nov.) Author:Moteki H, Azaiez H, Sloan-Heggen CM, Booth K, Nishio SY, Wakui K, Yamaguchi T, Kolbe DL, Iwasa YI, Shearer AE, Fukushima Y, Smith RJ, Usami SI.
Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients. PLoS One,11(9):e0162230 2016(Sep.) Author:Mori K, Moteki H, Miyagawa M, Nishio SY, Usami S.
An effective screening strategy for deafness in combination with a next-generation sequencing platform: a consecutive analysis. J Hum Genet,61(3):253-61 2016(Mar.) Author:Sakuma N, Moteki H, Takahashi M, Nishio SY, Arai Y, Yamashita Y, Oridate N, Usami S.
Correlation Between White Matter Lesions and Intelligence Quotient in Patients With Congenital Cytomegalovirus Infection. Pediatr Neurol,55:52-7 2016(Feb.) Author:Inaba Y, Motobayashi M, Nishioka M, Kaneko T, Yamauchi S, Kawasaki Y, Shiba N, Nishio SY, Moteki H, Miyagawa M, Takumi Y, Usami S, Koike K.
Advances in Molecular Genetics and the Molecular Biology of Deafness. Biomed Res Int,2016:5629093 2016 Author:Nishio SY, Schrauwen I, Moteki H, Azaiez H.
The effects of cochlear implantation in Japanese single-sided deafness patients: five case reports. Acta Otolaryngol,136(5):460-4 2016 Author:Kitoh R, Moteki H, Nishio S, Shinden S, Kanzaki S, Iwasaki S, Ogawa K, Usami S.
Silicone impression material foreign body in the middle ear: Two case reports and literature review AURIS NASUS LARYNX,42(5):419-423 2015(Oct.) Author:Suzuki, Nobuyoshi; Okamura, Koji; Yano, Takuya; Moteki, Hideaki; Kitoh, Ryosuke; Takumi, Yutaka; Usami, Shin-ichi;
Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY,124:177S-183S 2015(May) Author:Moteki, Hideaki; Azaiez, Hela; Booth, Kevin T.; Hattori, Mitsuru; Sato, Ai; Sato, Yoshihiko; Motobayashi, Mitsuo; Sloan, Christina M.; Kolbe, Diana L.; Shearer, A. Eliot; Smith, Richard J. H.; Usami, Shin-ichi;
Identification of a Novel CLRN1 Gene Mutation in Usher Syndrome Type 3: Two Case Reports ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY,124:94S-99S 2015(May) Author:Yoshimura, Hidekane; Oshikawa, Chie; Nakayama, Jun; Moteki, Hideaki; Usami, Shin-ichi;
De Novo Mutation in X-Linked Hearing Loss-Associated POU3F4 in a Sporadic Case of Congenital Hearing Loss ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY,124:169S-176S 2015(May) Author:Moteki, Hideaki; Shearer, A. Eliot; Izumi, Shuji; Kubota, Yamato; Azaiez, Hela; Booth, Kevin T.; Sloan, Christina M.; Kolbe, Diana L.; Smith, Richard J. H.; Usami, Shin-ichi;
Gene Expression Profiles of the Cochlea and Vestibular Endorgans: Localization and Function of Genes Causing Deafness ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY,124:6S-48S 2015(May) Author:Nishio, Shin-ya; Hattori, Mitsuru; Moteki, Hideaki; Tsukada, Keita; Miyagawa, Maiko; Naito, Takehiko; Yoshimura, Hidekane; Iwasa, Yoh-ichiro; Mori, Kentaro; Shima, Yutaka; Sakuma, Naoko; Usami, Shin-ichi;
The Patients Associated With TMPRSS3 Mutations Are Good Candidates for Electric Acoustic Stimulation ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY,124:193S-204S 2015(May) Author:Miyagawa, Maiko; Nishio, Shin-ya; Sakurai, Yuika; Hattori, Mitsuru; Tsukada, Keita; Moteki, Hideaki; Kojima, Hiromi; Usami, Shin-ichi;
Non-ocular Stickler Syndrome With a Novel Mutation in COL11A2 Diagnosed by Massively Parallel Sequencing in Japanese Hearing Loss Patients ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY,124:111S-117S 2015(May) Author:Iwasa, Yoh-ichiro; Moteki, Hideaki; Hattori, Mitsuru; Sato, Ririko; Nishio, Shin-ya; Takumi, Yutaka; Usami, Shin-ichi;
Novel Mutations in LRTOMT Associated With Moderate Progressive Hearing Loss in Autosomal Recessive Inheritance ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY,124:142S-147S 2015(May) Author:Ichinose, Aya; Moteki, Hideaki; Hattori, Mitsuru; Nishio, Shin-ya; Usami, Shin-ichi;
USH2 Caused by GPR98 Mutation Diagnosed by Massively Parallel Sequencing in Advance of the Occurrence of Visual Symptoms ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY,124:123S-128S 2015(May) Author:Moteki, Hideaki; Yoshimura, Hidekane; Azaiez, Hela; Booth, Kevin T.; Shearer, A. Eliot; Sloan, Christina M.; Kolbe, Diana L.; Murata, Toshinori; Smith, Richard J. H.; Usami, Shin-ichi;
Mutations in LOXHDI Gene Cause Various Types and Severities of Hearing Loss ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY,124:135S-141S 2015(May) Author:Mori, Kentaro; Moteki, Hideaki; Kobayashi, Yumiko; Azaiez, Hela; Booth, Kevin T.; Nishio, Shin-ya; Sato, Hiroaki; Smith, Richard J. H.; Usami, Shin-ichi;
Novel PTPRQ Mutations Identified in Three Congenital Hearing Loss Patients With Various Types of Hearing Loss ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY,124:184S-192S 2015(May) Author:Sakuma, Naoko; Moteki, Hideaki; Azaiez, Hela; Booth, Kevin T.; Takahashi, Masahiro; Arai, Yasuhiro; Shearer, A. Eliot; Sloan, Christina M.; Nishio, Shin-ya; Kolbe, Diana L.; Iwasaki, Satoshi; Oridate, Nobuhiko; Smith, Richard J. H.; Usami, Shin-ichi;
Mutations in the MYO15A Gene Are a Significant Cause of Nonsyndromic Hearing Loss: Massively Parallel DNA Sequencing-Based Analysis ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY,124:158S-168S 2015(May) Author:Miyagawa, Maiko; Nishio, Shin-ya; Hattori, Mitsuru; Moteki, Hideaki; Kobayashi, Yumiko; Sato, Hiroaki; Watanabe, Tomoo; Naito, Yasushi; Oshikawa, Chie; Usami, Shin-ichi;
Novel Mutations in GRXCRI at DFNB25 Lead to Progressive Hearing Loss and Dizziness ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY,124:129S-134S 2015(May) Author:Mori, Kentaro; Miyanohara, Ikuyo; Moteki, Hideaki; Nishio, Shin-ya; Kurono, Yuichi; Usami, Shin-ichi;
The advantages of sound localization and speech perception of bilateral electric acoustic stimulation ACTA OTO-LARYNGOLOGICA,135(2):147-153 2015(Feb.) Author:Moteki, Hideaki; Kitoh, Ryosuke; Tsukada, Keita; Iwasaki, Satoshi; Nishio, Shin-Ya; Usami, Shin-Ichi;
Evaluation of cortical processing of language by use of positron emission tomography in hearing loss children with congenital cytomegalovirus infection INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY,78(2):285-289 2014(Feb.) Author:Moteki, Hideaki; Suzuki, Mika; Naito, Yasushi; Fujiwara, Keizo; Oguchi, Kazuhiro; Nishio, Shin-ya; Iwasaki, Satoshi; Usami, Shin-ichi;
Effects of EAS cochlear implantation surgery on vestibular function ACTA OTO-LARYNGOLOGICA,133(11):1128-1132 2013(Nov.) Author:Tsukada, Keita; Moteki, Hideaki; Fukuoka, Hisakuni; Iwasaki, Satoshi; Usami, Shin-ichi;
TECTA mutations in Japanese with mid-frequency hearing loss affected by zona pellucida domain protein secretion JOURNAL OF HUMAN GENETICS,57(9):587-592 2012(Sep.) Author:Moteki, Hideaki; Nishio, Shin-ya; Hashimoto, Shigenari; Takumi, Yutaka; Iwasaki, Satoshi; Takeichi, Norihito; Fukuda, Satoshi; Usami, Shin-ichi;
舌下腺・口腔底切除術および広頸筋弁による再建術を行った舌下腺粘表皮癌の1例 頭頸部外科 = Journal of Japan Society for Head and Neck Surgery,22(1):53-57 2012(Jun. 30) Author:志摩 温; 岩崎 聡; 宮川 麻衣子; 茂木 英明; 三島 吉登; 宇佐美 真一; Keywords:唾液腺腫瘍; 舌下腺癌; 粘表皮癌; 広頸筋; 口腔;
Experience with the Vibrant Soundbridge RW-Coupler for round window Vibroplasty with tympanosclerosis ACTA OTO-LARYNGOLOGICA,132(6):676-682 2012(Jun.) Author:Iwasaki, Satoshi; Suzuki, Hiroaki; Moteki, Hideaki; Miyagawa, Maiko; Takumi, Yutaka; Usami, Shin-ichi;
Patients with CDH23 mutations and the 1555A > G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS) ACTA OTO-LARYNGOLOGICA,132(4):377-384 2012(Apr.) Author:Usami, Shin-ichi; Miyagawa, Maiko; Nishio, Shin-Ya; Moteki, Hideaki; Takumi, Yutaka; Suzuki, Mika; Kitano, Yoko; Iwasaki, Satoshi;
Language development in Japanese children who receive cochlear implant and/or hearing aid INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY,76(3):433-438 2012(Mar.) Author:Iwasaki, Satoshi; Nishio, Shinya; Moteki, Hideaki; Takumi, Yutaka; Fukushima, Kunihiro; Kasai, Norio; Usami, Shin-ichi;
Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients with GJB2 and SLC26A4 mutations ACTA OTO-LARYNGOLOGICA,131(11):1232-1236 2011(Nov.) Author:Moteki, Hideaki; Naito, Yasushi; Fujiwara, Keizo; Kitoh, Ryosuke; Nishio, Shin-ya; Oguchi, Kazuhiro; Takumi, Yutaka; Usami, Shin-ichi;
Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord ACTA OTO-LARYNGOLOGICA,131(9):976-982 2011(Sep.) Author:Furutate, Sakiko; Iwasaki, Satoshi; Nishio, Shin-ya; Moteki, Hideaki; Usami, Shin-ichi;
IgG4-related chronic rhinosinusitis: A new clinical entity of nasal disease ACTA OTO-LARYNGOLOGICA,131(5):518-526 2011(May) Author:Moteki, Hideaki; Yasuo, Masanori; Hamano, Hideaki; Uehara, Takeshi; Usami, Shin-ichi;
Achievement of hearing preservation in the presence of an electrode covering the residual hearing region ACTA OTO-LARYNGOLOGICA,131(4):405-412 2011(Apr.) Author:Usami, Shin-Ichi; Moteki, Hideaki; Suzuki, Nobuyoshi; Fukuoka, Hisakuni; Miyagawa, Maiko; Nishio, Shin-Ya; Takumi, Yutaka; Iwasaki, Satoshi; Jolly, Claude;
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