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聴覚・平衡覚研究部プロジェクト研究業績

2024

  • Minami S*, Takahashi M, Shinden S, Shirai K, Oishi N, Nishimura H, Masuda M, Masuda S, Nishiyama T, Hosoya M, Ueno M, Kashio A, Yamada H, Matsunaga T, Kaga K, Shintani A, Nemoto K. Prediction of cochlear implant effectiveness with surface-based morphometry. Otol Neurotol. 2024;45(2):114-120.
  • Udagawa T*, Takahashi E, Tatsumi N, Mutai H, Saijo H, Kondo Y, Atkinson PJ, Matsunaga T, Yoshikawa M, Kojima H, Okabe M, Cheng AG. Loss of Pax3 causes reduction of melanocytes in the developing mouse cochlea. Sci Rep. 2024 Jan 26;14(1):2210.
  • Hashimoto K, Miwa T, Ono C, Nara K, Mutai H, Seto T, Sakamoto H, Matsunaga T*. Gap Junction Beta-2 p.Val84Met Can Cause Autosomal Dominant Syndromic Hearing Loss With Keratoderma. Cureus. 2024 Feb; doi: 10.7759/cureus.54992.

2023

  • Yoshihama K, Mutai H, Sekimizu M, Ito F, Saito S, Nakamura S, Mikoshiba T, Nagai R, Takebayashi A, Miya F, Kosaki K, Ozawa H*, Matsunaga T*. Molecular basis of carotid body tumor and associated clinical features in Japan identified by genomic, immunohistochemical, and clinical analyses. Clin Genet. 2023;103(4):466-471
  • Tsuzuki N, Namba K, Saegusa C, Mutai H, Nishiyama T, Oishi N, Matsunaga T, Fujioka M*, Ozawa H. Apoptosis of type I spiral ganglion neuron cells in Otof-mutant mice. Neurosci Lett. 2023; 803:137178.
  • Yamazawa K*, Sugano K, Tanakaya K, Inoue S, Murakami H, Nakashima M, Adachi M, Oki S, Makabe T, Yamashita H, Ueki A, Sasaoka A, Nakashoji A, Kinoshita T, Matsunaga T, Arai M, Nakamura S, Miyata H, Ikegami M, Mano H, Kohsaka S, Matsui A. The pathogenic role of the BRCA2 c.7847C>T (p.Ser2616Phe) variant in breast and ovarian cancer predisposition. Cancer Sci. 2023; Jul;114(7):2993-3002.
  • Oishi1 N*, Noguchi M, Fujioka M, Nara K, Wasano K, Mutai H, Kawakita R, Tamura R, Karatsu K, Morimoto Y, Toda M, Ozawa H, Matsunaga T*. Correlation between genotype and phenotype with special attention to hearing in 14 Japanese cases of NF2 related schwannomatosis. Sci Rep. 2023; Apr 22;13(1):6595.
  • Yamamoto N, Balciuniene J, Hartman T, Diaz-Miranda MA, Bedoukian E, Devkota B, Lawrence A, Golenberg N, Patel M, Tare A, Chen R, Schindler E, Choi J, Kaur M, Charles S, Chen J, Fanning EA, Dechene E, Cao K, Jill MR, Rajagopalan R, Bayram Y, Dulik MC, Germiller J, Conlin LK, Krantz ID, Luo M*. Comprehensive Gene Panel Testing for Hearing Loss in Children: Understanding Factors Influencing Diagnostic Yield. J Pediatr. 2023; doi: 10.1016/j.jpeds.2023.113620. Epub ahead of print. PMID: 37473993.
  • 松永達雄*
    盲ろうの生理･病理学的特徴　In; 樫木暢子、金森克浩、船橋篤彦・編集. 特別支援教育免許シリーズ　重複障害教育領域①　複数の困難への対応
    建帛社: 東京　2023; 14－23
  • 松永達雄*
    ミトコンドリア難聴とはどのような疾患ですか？　In：村山圭、小坂仁、三牧正和・編集.ミトコンドリア病診療マニュアル2023
    診断と治療社：東京　2023; 258－259

2022

  • Masuda M, Kanno A, Nara K, Mutai H,Morisada N, Iijima K, Morimoto N, Nakano A, Sugiuchi T, Okamoto Y, Masuda S, Katsunuma S, Ogawa K, Matsunaga T*. Phenotype–genotype correlation in patients with typical and atypical branchio‑oto‑renal syndrome Sci Rep 2022; 12(1):969
  • Mutai H, Momozawa Y, Kamatani Y, Nakano A, Sakamoto H, Takiguchi T, Nara K, Kubo M, Matsunaga T*. Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes. Orphanet J Rare Dis 2022；17(1):114 doi: 10.1186/s13023-022-02262-4
  • 増田圭奈子、和佐野浩一郎、山野邉義晴、水野耕平、南修司郎、松永達雄*.　 患者におけるcVEMP測定体位選択の重要性　Equilib. res. 2022; 81(6): 491-501
  • 松永達雄*
    外耳奇形：大森孝一、野中学、小島博己・編集．標準耳鼻咽喉科・頭頸部外科学
    医学書院：東京　2022；52－53
  • 松永達雄*
    中耳奇形：大森孝一、野中学、小島博己・編集．標準耳鼻咽喉科・頭頸部外科学
    医学書院：東京　2022；54－56
  • 松永達雄*
    ミトコンドリア難聴 In :「小児内科」編集委員会 共編．小児内科2022 vol.54 特集症例から学ぶミトコンドリア病
    東京医学社：東京　2022；615－618
  • 松永達雄*
    遺伝学的検査の基本と最新情報
    耳鼻咽喉科・頭頸部外科 : 東京 2022; 94(12):1010-1013
  • 松永達雄*、山本 修子
    若年発症型両側性感音難聴の遺伝子診療
    耳鼻咽喉科展望 : 東京2022; 65(4):162-167(2022.08)
  • 勝沼紗矢香、松永達雄
    日本人類遺伝学会 生涯学習コンテンツ JSHG-WebCast ClinicalNotes : 東京 2022; CN_015.0
    https://jshg.jp/webcast_category/clinicalnotes/

2021

  • Matsunaga T*
    Clinical genetics, practice, and research of deafblindness: From uncollected experiences to the national registry in Japan.
    Auris Nasus Larynx 2021; 48(1): 185-193.
  • Yamazawa K*, Inoue T, Sakemi Y, Nakashima T, Yamashita H, Khono K, Fujita H, Enomoto K, Nakabayashi K, Hata K, Nakashima M, Matsunaga T, Nakamura A, Matsubara K, Ogata T, Kagami M. Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver–Russell syndrome. J Med Genet 2021; 58(6): 427-432.
  • Isobe A, Maeda N, Fujita H, Banno S, Kageyama T, Hatabu N, Sato R, Suzuki E, Miharu M, Komiyama O, Nakashima M, Matsunaga T, Nishimura G, Yamazawa K*. Metacarpophalangeal pattern profile analysis for a 3-monthold infant with Feingold syndrome 2. Am J Med Genet A 2021; 185(3): 952-954.
  • Masuda K*, Masuda M, Yamanobe Y, Mizuno K, Matsunaga T, Wasano K*. Effects on cervical vestibular-evoked myogenic potentials of four clinically used head and neck measurement positions in healthy subjects. Acta Otolaryngol 2021; 141(8): 729-735.
  • Hosoya M, Fujioka M, Nara K, Morimoto N, Masuda S, Sugiuchi T, Katsunuma S, Takagi A, Morita N, Ogawa K, Kaga K, Matsunaga T*. Investigation of the hearing levels of siblings affected by a single GJB2 variant: Possibility of genetic modifiers. Int J Pediatr Otorhinolaryngol 2021; 149(1): 110840.
  • Patel MJ, DiStefano MT, Oza AM, Hughes MY, Wilcox EH, Hemphill SE, Cushman BJ, Grant AR, Siegert RK, Shen J, Chapin A, Boczek NJ, Schimmenti LA, Nara K, Kenna M, Azaiez H, Booth KT, Avraham KB, Kremer H, Griffith AJ, Rehm HL, Amr SS, Tayoun ANA; ClinGen Hearing Loss Clinical Domain Working Group. Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss. Genet Med 2021; 23(11): 2208 – 2212.
  • Minami S*, Yamanobe Y, Nakano A, Sakamoto H, Masuda S, Takiguchi T, Katsunuma S, Sugiuchi T, Morita N, Kaga K, Matsunaga T*. A high risk of missing congenital cytomegalovirus-associated hearing loss through newborn hearing screening in Japan. J. Clin. Med 2021; 10(21): 5056.
  • Nakano A*, Arimoto Y, Mutai H, Nara K, Inoue S, Matsunaga T. Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts. Int J Pediatr Otorhinolaryngol 2022; 152(1):110975 doi.10.1016/j.ijporl.2021.110975.
  • Yamazawa K*, Shimizu K, Ohashi H, Haruna H, Inoue S, Murakami H, Matsunaga T, Iwata T, Tsunoda K, Fujinami K. A Japanese boy with double diagnoses of 2p15p16.1 microdeletion syndrome and RP2-associated retinal disorder. Hum Genome Var 2021; 8(1): 46.
  • 松永達雄*
    クロマチンリモデリング因子異常症　CHARGE 症候群: 副島英伸、秦健一郎　編集
    遺伝子医学Mook 36号　エピゲノムで新たな解明が進む「先天性疾患.
    メディカルドゥ: 東京　2021; 151-157
  • 松永達雄*
    ワルデンブルグ症候群 In :「小児内科」「小児外科」編集委員会 共編．
    小児内科2021 vol.53 小児疾患診療のための病態生理2
    東京医学社：東京　2021；203-205

2020

  • Yamamoto N, Mutai H, Namba K, Goto F, Ogawa K, Matsunaga T*. Clinical profiles of DFNA11 at diverse stages of development and　aging in a large family identified by linkage analysis. Otol Neurotol 2020; 41(6): e663-e673.
  • Mutai H, Wasano K, Momozawa Y, Kamatani Y, Miya F, Masuda S, Morimoto N, Nara K, Takahashi S, Tsunoda T, Homma K, Kubo M, Matsunaga T*. Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans. PLoS Genet 2020;16(4): e1008643.
  • Fujioka M*, Akiyama T, Hosoya M, Kikuchi K, Fujiki Y, Saito Y, Yoshihama K, Ozawa H, Tsukada K, Nishio S, Usami S, 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; 99(19): e19763.
  • Fujioka M, Hosoya M, Nara K, Morimoto N, Sakamoto H, Otsu M, Nakano A, Arimoto Y, Masuda S, Sugiuchi T, Masuda S, Morita N, Ogawa K, Kaga K, Matsunaga T*. Differences in hearing levels between siblings with hearing loss caused by GJB2 mutations. Auris Nasus Larynx 2020; 47(6): 938-942.
  • Watabe T, Kanzaki S*, Sato N, Matsunaga T, Muramatsu M, Ogawa K. Single nucleotide polymorphisms in tinnitus patients exhibiting severe distress. Sci Rep 2020; 10(1): 13023.
  • Wasano K*, Takahashi S, Rosenberg SK, Kojima T, Mutai H, Matsunaga T, Ogawa K, Homma K*. Systematic quantification of the anion transport function of pendrin (SLC26A4) and its disease‐associated variants. Hum Mutat 2020; 41(1): 316–331.
  • 仲野敦子、有本友季子、務台英樹、松永達雄． GJB2遺伝子変異が検出された小児難聴症例の臨床経過と遺伝学的検査． 日本耳鼻咽喉科学会会報. 2020; 123(1): 1225-1230.
  • 松永達雄
    急性感音難聴acute sensorineural hearing loss：福井次矢、高木誠、小室一成　総編集.　今日の治療指針 2020年版（私はこう治療している）
    医学書院：東京　2020; 1593-1594
  • 松永達雄
    ミトコンドリア病の臨床病型　ミトコンドリア難聴: 村山圭、小坂仁、三牧正和　編集
    遺伝子医学Mook 35号「ミトコンドリアと病気」
    メディカルドゥ: 東京　2020；125-131
  • 松永達雄*
    小児の難聴 小児内科 Vol.52 No.8, 2020-8
    東京医学社：東京　2020; 1090-1094

2019

  • Kitao K, Mutai H, Namba K, Morimoto N, Nakano A, Arimoto Y, Sugiuchi T, Masuda S, Okamoto Y, Morita N, Sakamoto H, Shintani T, Fukuda S, Kaga K, Matsunaga T*. Deterioration in distortion product otoacoustic emissions in auditory neuropathy patients with distinct clinical and genetic backgrounds. Ear Hear 2019; 40(1): 184-191.
  • Hatabu N, Katori N, Sato T, Maeda N, Suzuki E, Komiyama O, Tsutsui H, Nagao T, Nakauchi-Takahashi H, Matsunaga T, Ishii T, Hasegawa T, Yamazawa K*. A familial case of a whole germline CDC73 deletion discordant for primary hyperparathyroidism. Horm Res Paediatr 2019; 92(1): 56-63.
  • 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., Abou Tayoun AN., Amr SS* on behalf of the ClinGen Hearing Loss Clinical Domain Working Group. ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs. Genet Med 2019; 21(10): 2239 – 2247.
  • Minami S, Nara K, Mutai H, Morimoto N, Sakamoto H, Takiguchi T, Kaga K, Matsunaga T*. A clinical and genetic study of 16 Japanese families with Waardenburg syndrome. Gene 2019; 704 (1): 86-90.
  • Shen J*, Oza AM, Castillo I, Duzkale H, Matsunaga T, Pandya A, Kang HP, Mar-Heyming R, Guhan S, Moyer K, Lo C, Kenna M, Alexander JJ, Zhang Y, Hirsch Y, Luo M, Cao Y, Choy KW, Cheng YF, Avraham KB, Hu X, Garrido G, Moreno-Pelayo MA, Greinwald J, Zhang K, Zeng Y, Brownstein Z, Basel-Salmon L, Davidov B, Frydman M, Weiden T, N agan N, Willis A, Hemphill SE, Grant AR, Siegert RK, DiStefano MT, Amr SS, Rehm HL, Abou Tayoun AN* on behalf of the ClinGen Hearing Loss Working Group. Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel. Genet Med 2019; 21 (11): 2442 – 2452.
  • Maeda-Katahira A, Nakamura N, Hayashi T, Katagiri S, Shimizu S, Ohde H, Matsunaga T, Kaga K, Nakano T, Kameya S, Matsuura T, Fujinami K, Iwata T, Tsunoda K*. Autosomal dominant optic atrophy with OPA1 gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohort. Mol Vis 2019; 25 (1): 559-573.
  • 山本修子、南修司郎、榎本千江子、加藤秀敏、松永達雄、伊藤文展、遠藤理奈子、橋本陽介、石川直明、加我君孝. 東京医療センターにおける成人人工内耳症例の適応と有用性の検討. 日本耳鼻咽喉科学会会報. 2019; 122(8): 1118-1126.
  • 松永達雄*
    耳介・外耳道の先天異常（耳瘻孔を含む）congenital anomalies of auricle and external ear canal　In：福井次矢、高木誠、小室一成　総編集.　今日の治療指針 2019年版（私はこう治療している）
    医学書院：東京　2019; 1545
  • 松永達雄*
    「第119回日本耳鼻咽喉科学会総会シンポジウム」難聴のゲノム医療.
    日本耳鼻咽喉科学会会報［Nippon Jibiinkoka Gakkai Kaiho (Tokyo)］. 2019:122:16-21
  • 松永達雄*.
    視覚聴覚二重障害の診療.
    JOHNS Vol. 35 No.9 2019: 1377-1378頁.
    2019年9月発行
  • 松永達雄*.
    遺伝情報をどう管理し、活用するか―耳科領域―.
    JOHNS Vol. 35 No.10 2019: 1452-1454頁.
    2019年9月発行

2018

  • Yamazawa K, Yamada Y, Kuroda T, Mutai H, Matsunaga T, Komiyama O, Takahashi T. Spontaneous intramural duodenal hematoma as the manifestation of Noonan syndrome. Am J Med Genet A. 2018; 176(2):496-498.
  • Unzaki A, Morisada N*, Nozu K, Ye MJ, Ito S, Matsunaga T, Ishikura K, Ina S, Nagatani K, Okamoto T, Inaba Y, Ito N, Igarashi T, Kanda S, Ito K, Omune K, Iwaki T, Ueno K, Yahata M, Ohtsuka Y, Nishi E, Takahashi N, Ishikawa T, Goto S, Okamoto N, Iijima K. Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome. J Hum Genet 2018; 63(5):647–656.
  • Matsushima K, Nakano A, Arimoto Y, Mutai H, Yamazawa K, Murayama K, Matsunaga T*. High-level heteroplasmy for the m.7445A>G mitochondrial DNA mutation can cause progressive sensorineural hearing loss in infancy. Int J Pediatr Otorhinolaryngol. 2018; 108:125-131.
  • Shigemizu D*, Miya F, Akiyama S, Okuda S, Boroevich KA, Fujimoto A, Nakagawa H, Ozaki K, Niida S, Kanemura Y, Okamoto N, Saitoh S, Kato M, Yamasaki M, Matsunaga T, Mutai H. Kosaki K, Tsunoda T*. IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis. Sci Rep 2018; 8(1): 5608.
  • Morimoto N, Mutai H, Namba K, Kaneko H, Kosaki R, Matsunaga T*. Homozygous EDNRB Mutation in a Patient with Waardenburg Syndrome Type 1. Auris Nasus Larynx 2018; 45(2):222-226.
  • Suzuki N, Mutai H, Miya F, Tsunoda T, Terashima H, Morimoto N, Matsunaga T*. A case report of reversible generalized seizures in a patient with Waardenburg syndrome associated with a novel nonsense mutation in the penultimate exon of SOX10. BMC Pediatr. 2018; 18(1):171.
  • Matsunaga T*, Matsushima K, Murayama K. Response to “Infantile-onset deafness in m.7445A>G carriers may be multicausal”. Int J Pediatr Otorhinolaryngol 2018; 111:194.
  • Oza AM, DiStefano MT, Hemphill SE, Cushman BJ, Grant AR, Siegert RK, Shen J, Chapin A, Boczek NJ, Schimmenti LA, Murry JB, Hasadsri L, Nara K, Kenna M, Booth KT, Azaiez H, Griffith A, Avraham KB, Kremer H, Rehm HL, Amr SS, Abou Tayoun AN*, ClinGen Hearing Loss Clinical Domain Working Group. Expert specification of the ACMG/AMPvariant interpretation guidelines for genetic hearing loss. Hum Mutat. 2018; 39(11):1593-1613.
  • Mutai H*, Miya F, Shibata H, Yasutomi Y, Tsunoda T, Matsunaga T. Gene expression dataset for whole cochlea of Macaca fascicularis. Sci Rep. 2018; 8(1):15554.
  • Hosoya M, Minami SB*, Enomoto C, Matsunaga T, Kaga K. Elongated EABR Wave Latencies Observed in Patients With Auditory Neuropathy Caused by OTOF Mutation. Laryngoscope Investig Otolaryngol. 2018; 3(5):388-393.
  • Suzuki H, Kurosawa K, Fukuda K, Ijima K, Sumazaki R, Saito S, Kosaki R, Hirasawa A, Okazaki Y, Imai K, Matsunaga T, Iwata T, Kosaki K*. Japanese pathogenic variant database: DPV. Transl Sci Rare Dis. 2018;3:133–137.
  • Hosoya M, Saeki T, Saegusa C, Matsunaga T, Okano H, Fujioka M*, Ogawa K. Estimating the concentration of therapeutic range using disease-specific iPS cells: Low-dose rapamycin therapy for Pendred syndrome. Regen Ther 2018;10: 54-63.
  • 増田圭奈子*、五島史行、松永達雄.　小児めまいの問診票（日本語版DHI-PC）の有用性の検討.
    Otol Jpn. 2018; 28(5):708-714
  • 松永達雄
    遺伝性難聴の診断の進歩　In：山岨達也　編集．医学のあゆみBOOKS 耳鼻咽喉科診療の進歩　40のエッセンス
    医歯薬出版：東京　2018; 7-10
  • 松永達雄
    前庭水管拡大症　In：森山寛　監修．大森孝一、藤枝重治、小島博己、猪原秀典　編集．今日の耳鼻咽喉科・頭頸部外科治療指針　第4版
    医学書院：東京　2018; 257-258
  • 松永達雄
    先天性難聴児のゲノム診療の意義と動向
    公衆衛生 2018; 82(6)468-473
  • 松永達雄
    遺伝学的診療の進め方
    耳鼻咽喉科・頭頸部外科 2018;90(8):598-604
  • 松永達雄
    臨床像起点の遺伝性難聴診療の確立.
    Otol Jpn. 2018;28(2):65-69.
  • 松永達雄
    ゲノム医療(遺伝子医療)の今　希少疾患・難病の遺伝カウンセリング.
    保健の科学.  2018;60(10) 677-681.

2017

  • Kanno A, Mutai M, Namba K, Morita N, Nakano A, Ogahara N, Sugiuchi T, Ogawa K, Matsunaga T. Frequency and Specific Characteristics of the Incomplete Partition Type III Anomaly in Children. Laryngoscope 2017; 127:1662-1669
  • Hosoya M, Fujioka M, Sone T, Okamoto S, Akamatsu W, Ukai H, Ueda HR, Ogawa K, Matsunaga T, Okano H. Cochlear cell modeling using disease-specific iPSCs unveils a degenerative phenotype and suggests treatments for congenital progressive hearing loss. Cell Rep. 2017; 18(1):68-81
  • Kasakura-Kimura N, Masuda M, Mutai H, Masuda S, Morimoto N, Ogahara N, Misawa H, Sakamoto H, Saito K, Matsunaga T*. WFS1 and GJB2 mutations in patients with bilateral low-frequency sensorineural hearing loss. Laryngoscope 2017; 127:E324–E329
  • Mutai H, Watabe T, Kosaki K, Ogawa K, Matsunaga T. Mitochondrial mutations in maternally inherited hearing loss. BMC Medical Genetics 2017;18(1):32
  • Kitoh R, Nishio S, Ogawa K, Kanzaki S, Hato N, Sone M, Fukuda S, Hara A, Ikezono T, Ishikawa K, Iwasaki S, Kaga K, Kakehata S, Matsubara A, Matsunaga T, Murata T, Naito Y, Nakagawa T, Nishizaki K, Noguchi Y, Sano H, Sato H, Suzuki M, Shojaku H, Takahashi H, Takeda H, Tono T, Yamashita H, Yamasoba T, Usami S. Nationwide epidemiological survey of idiopathic sudden sensorineural hearing loss in Japan. Acta Oto-Laryngologica 2017; 137(sup565):S8-S16
  • Umesawa M, Kobashi G, Kitoh R, Nishio S, Ogawa K, Hato N, Sone M, Fukuda S, Hara A, Ikezono T, Ishikawa K, Iwasaki S, Kaga K, Kakehata S, Matsubara A, Matsunaga T, Murata T, Naito Y, Nakagawa T, Nishizaki K, Noguchi Y, Sano H, Sato H, Suzuki M, Shojaku H, Takahashi H, Takeda H, Tono T, Yamashita H, Yamasoba T, Usami S. Relationships among drinking and smoking habits, history of diseases, body mass index and idiopathic sudden sensorineural hearing loss in Japanese patients. Acta Oto-Laryngologica 2017; 137(sup565):S17-S23
  • Okada M, Hato N, Nishio S, Kitoh R, Ogawa K, Kanzaki S, Sone M, Fukuda S, Hara A, Ikezono T, Ishikawa K, Iwasaki S, Kaga K, Kakehata S, Matsubara A, Matsunaga T, Murata T, Naito Y, Nakagawa T, Nishizaki K, Noguchi Y, Sano H, Sato H, Suzuki M, Shojaku H, Takahashi H, Takeda H, Tono T, Yamashita H, Yamasoba T, Usami S. The effect of initial treatment on hearing prognosis in idiopathic sudden sensorineural hearing loss: a nationwide survey in Japan. Acta Oto-Laryngologica 2017; 137(sup565):S30-S33
  • Sato H, Kuwashima S, Nishio S, Kitoh R, Fukuda S, Hara A, Hato N, Ikezono T, Ishikawa K, Iwasaki S, Kaga K, Matsubara A, Matsunaga T, Murata T, Naito Y, Nakagawa T, Nishizaki K, Noguchi Y, Ogawa K, Sano H, Sone M, Shojaku H, Takahashi H, Tono T, Yamashita H, Yamasoba T, Usami S. Epidemiological survey of acute low-tone sensorineural hearing loss. Acta Oto-Laryngologica 2017; 137(sup565):S34-S37
  • Yoshida T, Sone M, Kitoh R, Nishio S, Ogawa K, Kanzaki S, Hato N, Fukuda S, Hara A, Ikezono T, Ishikawa K, Iwasaki S, Kaga K, Kakehata S, Matsubara A, Matsunaga T, Murata T, Naito Y, Nakagawa T, Nishizaki K, Noguchi Y, Sano H, Sato H, Suzuki M, Shojaku H, Takahashi H, Takeda H, Tono T, Yamashita H, Yamasoba T, Usami S. Idiopathic sudden sensorineural hearing loss and acute low-tone sensorineural hearing loss: a comparison of the results of a nationwide epidemiological survey in Japan. Acta Oto-Laryngologica 2017; 137(sup565):S38-S43
  • Morita S, Fujiwara K, Fukuda A, Fukuda S, Nishio S, Kitoh R, Hato N, Ikezono T, Ishikawa K, Kaga K, Matsubara A, Matsunaga T, Murata T, Naito Y, Nishizaki K, Ogawa K, Sano H, Sato H, Sone M, Suzuki M, Takahashi H, Tono T, Yamashita H, Yamasoba T, Usami S. The clinical features and prognosis of mumps-associated hearing loss: a retrospective, multi-institutional investigation in Japan. Acta Oto-Laryngologica 2017; 137(sup565):S44-S47
  • Wada T, Sano H, Nishio S, Kitoh R, Ikezono T, Iwasaki S, Kaga K, Matsubara A, Matsunaga T, Murata T, Naito Y, Suzuki M, Takahashi H, Tono T, Yamashita H, Hara A, Usami S. Differences between acoustic trauma and other types of acute noise-induced hearing loss in terms of treatment and hearing prognosis. Acta Oto-Laryngologica 2017; 137(sup565):S48-S52
  • Kaneko Y, Nakano A, Arimoto Y, Nara K, Mutai H, Matsunaga T. The first sporadic case of DFNA11 identified by next-generation sequencing. Int J Pediatr Otorhinolaryngol 2017; 100:183-186
  • Yamamoto N, Mutai H, Namba K, Morita N, Masuda S, Nishi Y, Nakano A, Masuda S, Fujioka M, Kaga K, Ogawa K, Matsunaga T. Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss. Orphanet J Rare Dis. 2017; 12:157
  • Cheng Y, Nakamura M, Matsunaga T, Kaga K. A case of auditory neuropathy revealed by OTOF gene mutation analysis in a junior high school girl. J Otol. 2017; 12: 202-206
  • 松永達雄.
    「聴力低下がある」と言われたら　
    In：伊藤澄信・編集. 健診データで困ったら　よくある検査異常への対応策.
    医学書院：東京　2017; 20-23
  • 松永達雄*.
    遺伝性難聴と内耳再生医療.
    日本医事新報：東京　2017; 4846:29
  • 加我君孝*、松永達雄.
    Auditory neuropathy と auditory neuropathy spectrum disorders　聴覚障害の病態生理と難聴遺伝子変異
    耳鼻咽喉科・頭頸部外科：東京　2017; 89(7):530–542
  • 南修司郎、榎本千江子、加藤秀敏、山本修子、細谷誠、若林毅、利國桂太郎、松永達雄、加我君孝.
    当医療センターで初回人工内耳手術を行った聴覚障害児138児の療育先及びその後の就学状況調査.
    耳鼻咽喉科・頭頸部外科 2017; 89(3): 265-269

2016

  • Masuda M, Mutai H, Arimoto Y, Nakano A, Matsunaga T. A novel frameshift variant of COCH supports the hypothesis that haploinsufficiency is not a cause of autosomal dominant nonsyndromic deafness 9. Biochem Biophys Res Commun 2016; 469(2): 270-274
  • Namba K, Mutai H, Takiguchi Y, Yagi H, Okuyama T, Oba S, Yamagishi R, Kaneko H, Shintani T, Kaga K, Matsunaga T. Molecular impairment mechanisms of novel OPA1 mutations predicted by molecular modeling in patients with autosomal dominant optic atrophy and auditory neuropathy spectrum disorder. Otol Neurotol 2016; 37(4): 394-402
  • Matsunaga T, Morimoto N. The auditory phenotype of children harboring mutations in the prestin gene. Acta Otolaryngol 2016;136(4):397-401
  • Minami SB, Mutai H, Namba K, Sakamoto K, Matsunaga T. Clinical characteristics of a Japanese family with hearing loss accompanied by compound heterozygous mutations in LOXHD1. Auris Nasus Larynx 2016; 43(6):609-613
  • Wasano K, Matsunaga T, Ogawa K, Kunishima S. Late onset and high-frequency dominant hearing loss in a family with MYH9 disorder. Eur Arch Otorhinolaryngol 2016; 273:3547 – 3552
  • Takano K, Ogasawara N, Matsunaga T, Mutai H, Sakurai A, Ishikawa A, Himi T. A novel nonsense mutation in the NOG gene causes familial NOG-related symphalangism spectrum disorder. Hum Genome Variation 2016; 3:16023
  • Kitao K, Mizutari K, Nakagawa S, Matsunaga T, Fukuda S, Fujii M. Recovery of endocochlear potential after severe damage to lateral wall fibrocytes following acute cochlear energy failure. Neuroreport 2016; 27(15):1159-1166
  • Goto F, Arai M, Kitamura M, Otomo A, Nagai R, Shimada T, Minami S, Matsunaga T, Tsunoda K, Fujii M. A case of undiagnosed sleep disorder complaining hearing difficulty and dizziness. Iran J Otorhinolaryngol 2016; 28(85):149-152.
  • Yamamoto N, Kanno A, Matsunaga T. Genetics of Inner Ear Malformation and Cochlear Nerve Deficiency. In: Cochlear Implantation in Children with Inner Ear Malformation and Cochlear Nerve Deficiency. Kaga K (Ed.). Springer: Tokyo. 2016; 47-59
  • 松永達雄
    ミトコンドリアDNAの遺伝子変異によるアミノグリコシドの副作用（感音難聴）の発症予測　
    In：奥山虎之、山本俊至・編集．遺伝学的検査・診断・遺伝カウンセリングの上手な進めかた
    診断と治療社：東京　2016; 166-168
  • 松永達雄
    遺伝子診断・平衡障害
    In：永井良三・シリーズ総監修. 山岨達也、小川郁、丹生健一、久育男、森山寛、宇佐美真一・編集．耳鼻咽喉科・頭頚部外科研修ノート改訂第２版
    診断と治療社：東京　2016; 622
  • 松永達雄
    新しい検査・解釈　遺伝子とめまい疾患
    JOHNS：東京　2016; 32(1): 45-48
  • 永井遼斗、松永達雄
    図説シリーズ「目で見る遺伝医学」－難聴の遺伝医学　
    国立医療学会誌「医療」：東京　 2016 ; 70(3) : 160-166.
  • 松永達雄、山本修子、村山圭
    指定難病制度を踏まえたミトコンドリア病の診療.
    耳鼻咽喉科・頭頸部外科：東京　2016 ; 88(3) : 240-247.
  • 松永達雄（協力）
    聴覚と平衡感覚のしくみ
    Newton（2016.2.7発行）：東京　2016; 36(2):98-109
  • 船越公威、田島木綿子、松永達雄、宋文杰、小畑千尋、井須尚紀、犬塚則久（協力）
    聴覚のしくみ．
    Newton 別冊（2016.3.25.発行）：東京　2016 ; 90-123

2015

  • Yamashita D, Sun G, Cui Y, Mita S, Otsuki N, Kanzaki S, Nibu K, Ogawa K, Matsunaga T. Neuroprotective effects of cutamesine, a ligand of the sigma-1 receptor 1 chaperone, against noise-induced hearing loss. J Neurosci Res 2015;93:788–795
  • Mutai H, Miya F, Fujii M, Tsunoda T, Matsunaga T. Attenuation of Progressive Hearing Loss in DBA/2J Mice by Reagents that Affect Epigenetic Modifications Is Associated with Up-Regulation of the Zinc Importer Zip4. PLoS ONE 2015; 10(4): e0124301. doi:10.1371/journal.pone.0124301
  • Mizutari K, Mutai H, Namba K, Miyanaga Y, Nakano A, Arimoto Y, Masuda S, Morimoto N, Sakamoto H, Kaga K, Matsunaga T. High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss. Orphanet J Rare Dis 2015;10(1):60. doi: 10.1186/s13023-015-0276-z.
  • Wasano K, Mutai H, Obuchi C, Masuda S, Matsunaga T. A novel frameshift mutation in KCNQ4 in a family with autosomal recessive non-syndromic hearing loss. Biochem Biophys Res Commun 2015; 463: 582-586
  • Miya F, Mutai H, Fujii M, Boroevich KA, Matsunaga T, Tsunoda T. Gene expression profiling of DBA/2J mice cochleae treated with L-methionine and valproic acid. Genomic Data 2015; 5: 323-325
  • 松永達雄
    突発性難聴　In：福井次夫、高木誠、小室一成・総編集．今日の治療指針 2015年版
    医学書院：東京　2015;1410-1411
  • 松永達雄
    外リンパ瘻　In：福井次夫、高木誠、小室一成・総編集．今日の治療指針 2015年版
    医学書院：東京　2015;1411-1412
  • 大友章子、南修司郞、永井遼斗、松永達雄、榎本千江子、坂田英明、藤井正人、加我君孝
    Waardenburg症候群2型に対する人工内耳埋め込み術後の聴覚・言語発達
    耳鼻咽喉科・頭頸部外科：東京 2015:87(2):173-175
  • 松永達雄
    先天性難聴児の遺伝子変異の研究と診療における新しい動向
    音声言語医学：東京 2015;56(3):219-225
  • 松永達雄、瀧口洋一郎
    突発性難聴の病態.
    耳鼻咽喉科・頭頸部外科：東京 2015:87(8):564–572
  • 松永達雄
    Waardenburg症候群　In：『小児内科』『小児外科』編集委員会共編．小児内科2015年47巻増刊号．
    株式会社東京医学社：東京　2015;210-212.

2014

  • Masuda S, Namba K, Mutai H, Usui S, Miyanaga Y, Kaneko H, Matsunaga T. A Mutation in the Heparin-Binding Site of Noggin as a Novel Mechanism of Proximal Symphalangism and Conductive Hearing Loss. Biochem Biophys Res Commun 2014;447(3):496-502
  • Arimoto Y, Namba K, Nakano A, Matsunaga T. Chronic constipation recognized as a sign of a SOX10 mutation in a patient with Waardenburg syndrome. Gene 2014;540:258-262
  • Matsunaga T.
    Etiology and Genes.
    In：Microtia and Atresia – Combined Approach by Plastic and Otologic Surgery. Adv Otorhinolaryngol. Kaga K, Asato H (Eds). Karger, Basel 2014;75:2-8
  • Fujioka M, Okamoto Y, Shinden S, Okano HJ, Okano H, Ogawa K, Matsunaga T.
    Pharmacological inhibition of cochlear mitochondrial respiratory chain induces secondary inflammation in the lateral wall: a potential therapeutic target for sensorineural hearing loss. PLoS ONE 2014;9(3):1-7
  • Okamoto Y, Mutai H, Nakano A, Arimoto Y, Sugiuchi T, Masuda S, Morimoto N, Sakamoto H, Ogahara N, Takagi A, Taiji H, Kaga K, Ogawa K, Matsunaga T． Subgroups of enlarged vestibular aqueduct in relation to SLC26A4 mutations and hearing loss． Laryngoscope 2014;124: E134-E140
  • 松永達雄
    急性感音難聴
    In:福井次夫、高木誠、小室一成・総編集.　今日の治療指針　2014年版
    医学書院：東京 2014; 1352-1353
  • 松永達雄
    Auditory Neuropathy Spectrum Disorders　In：加我君孝・編集. 新生児・幼小児の難聴－遺伝子診断から人工内耳手術、療育・教育まで－
    診断と治療社：東京 2014;26-29
  • 松永達雄
    難聴遺伝子変異　In：加我君孝・編集. 新生児・幼小児の難聴－遺伝子診断から人工内耳手術、療育・教育まで－
    診断と治療社：東京2014;19-25
  • 松永達雄　
    Pendred症候群の診断と治療
    日耳鼻会報 2014; 117: 144-145
  • 松永達雄
    よくわかる遺伝子　単一遺伝子異常と疾患　難聴と内分泌の異常
    JOHNS：東京 2014; 30(6): 741-744
  • 松永達雄
    難聴の遺伝子診断・遺伝子治療
    脳21：京都　 2014;17(3):290-292

2013

  • Mutai H, Suzuki N, Shimizu A, Torii C, Namba K, Morimoto N, Kudoh J, Kaga K, Kosaki K, Matsunaga T. Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: A cross-sectional, multi-center next-generation sequencing study. Orphanet J. Rare Dis 2013;8(1):172
  • Minami SB, Mutai H, Nakano A, Arimoto Y, Taiji H, Morimoto N, Sakata H, Adachi N, Masuda S, Sakamoto H, Yoshida H, Tanaka F, Morita N, Sugiuchi T, Kaga K, Matsunaga T． GJB2-associated hearing loss undetected by hearing screening of newborns． Gene 2013; 532(1):41-45
  • Takiguchi Y, Sun G, Ogawa K, Matsunaga T. Long-lasting changes in the cochlear K+ recycling structures after acute energy failure Neurosci Res 2013;77(1-2):33-41
  • Matsunaga T, Mutai H, Namba K, Morita N, Masuda S. Genetic analysis of PAX3 for diagnosis of Waardenburg syndrome type I Acta Otolaryngol 2013;133(4): 345-51
  • Watabe T, Matsunaga T, Namba K, Mutai H, Inoue Y, Ogawa K． Moderate hearing loss associated with a novel KCNQ4 non-truncating mutation located near the N-terminus of the pore helix Biochem Biophys Res Commun 2013; 432(3): 475-479
  • Nakano A, Arimoto Y, Matsunaga T Cochlear nerve deficiency and associated clinical features in patients with bilateral and unilateral hearing loss Otol Neurotol 2013; 34(3): 554-558
  • Masuda S, Usui S, Matsunaga T High prevalence of inner-ear and/or internal auditory canal malformations in children with unilateral sensorineural hearing loss Int J Pediatr Otorhinolaryngol 2013; 77:228-232
  • 松永達雄、藤岡正人、細谷誠
    Pendred症候群研究の現況と展望
    日本臨牀：大阪　 2013; 71(12): 2215 – 2222
  • 松永達雄、鈴木直大、務台英樹、難波一徳、加我君孝
    次世代シークエンサーを用いた難聴の遺伝子診断に関する検討
    Otol Jpn 2013; 23(5): 903-907

2012

  • Taiji H, Morimoto N, Matsunaga T Unilateral cochlear nerve hypoplasia in children with mild to moderate hearing loss Acta Otolaryngol 2012:132(11):1160-7
  • Matsunaga T, Mutai H, Kunishima S, Namba K, Morimoto N, Shinjo Y, Arimoto Y, Kataoka Y, Shintani T, Morita N, Sugiuchi T, Masuda S, Nakano A, Taiji H, Kaga K A prevalent founder mutation and genotype-phenotype correlations of OTOF in Japanese patients with auditory neuropathy Clin Genet 2012:82:425-432
  • Minami SB, Masuda S, Usui S, Mutai H, Matsunaga T Comorbidity of GJB2 and WFS1 mutations in one family Gene 2012:501(2):193-197
  • Sun G, Fujii M, Matsunaga T Functional Interaction between Mesenchymal Stem Cells (MSCs) and Spiral Ligament Fibrocytes (SLFs) J Neurosci Res 2012 90(9):1713-22
  • Namba K, Mutai H, Kaneko H, Hashimoto S, Matsunaga T In silico modeling of the pore region of a KCNQ4 missense mutant from a patient with hearing loss BMC Research Notes 2012;5:145
  • Fujinami Y, Mutai H, Mizutari K, Nakagawa S, Matsunaga T A novel animal model of hearing loss caused by acute endoplasmic reticulum stress in the cochlea. J Pharmcol Sci 2012;118:363-372:
  • 松永達雄
    難聴
    In:泉孝英・編集.　今日の診療のために　ガイドライン外来診療2012
    日経メディカル開発：東京　2012; 505-507　
  • 仲野敦子、有本友季子、松永達雄、工藤典代
    Otoferlin遺伝子変異が確認された小児難聴症例の検討
    Otol Jpn 22(1):47-52, 2012　
  • 仲野敦子、有本有季子、松永達雄、工藤典代
    側頭骨CTで両側蝸牛神経管狭窄を認めた小児難聴症例の検討
    日耳鼻会報：東京　115(9)849-854,2012

2011

  • Mutai H, Kouike H, Teruya E, Takahashi-Kodomoari I, Kakishima H, Taiji H, Usami S, Okuyama T, Matsunaga T Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation BMC Medical Genetics 2011;12:35
  • Mizutari K, Nakagawa S, Mutai H, Fujii M, Ogawa K, Matsunaga T Late-phase recovery in the cochlear lateral wall following severe degeneration by acute energy failure. Brain Res 2011;1419: 1-11
  • Cui Y, Sun GW, Yamashita D, Kanzaki S, Matsunaga T, Fujii M, Kaga K, Ogawa K Acoustic overstimulation-induced apoptosis in fibrocytes of the cochlear spiral limbus of mice. Eur Arch Otorhinolaryngol 268 (7), 973-978, 2011
  • 松永達雄
    Auditory Neuropathyの遺伝子
    Clinical Neuroscience 29 (12) 1409 – 1411, 2011
  • 大原卓哉、泰地秀信、守本倫子、本村朋子、松永達雄
    OTOF遺伝子変異を認めるAuditory neuropathy spectrum disorderの乳幼児例における人工内耳装用効果
    Audiology Japan 54 (4) 289 – 297, 2011　
  • 松永達雄
    ステロイド依存性感音難聴
    JOHNS：東京 27 (9) 1352 – 1353, 2011
  • 松永達雄（監修）
    平衡感覚を取り戻す人工内耳
    別冊日経サイエンス：東京　177「先端医療をひらく」p126-130　2011年1月17日　日経サイエンス社

2010

  • Fujinami Y, Mutai H, Kamiya K, Mizutari K, Fujii M, Matsunaga T. Enhanced expression of C/EBP homologous protein (CHOP) precedes degeneration of fibrocytes in the lateral wall after acute cochlear mitochondrial dysfunction induced by 3-nitropropionic acid Neurochem Int 2010;56 (3) 487 – 494
  • Mizutari K, Matsunaga T, Inoue Y, Kaneko H, Yagi H, Namba K, Shimizu S, Kaga K, Ogawa K. Vestibular dysfunction in a Japanese patient with a mutation of the gene OPA1. J Neurol Sci 2010;293 (1-2):23-28
  • Mizutari K, Fujioka M, Nakagawa S, Fujii , Ogawa K, Matsunaga T Balance dysfunction resulting from acute inner ear energy failure is caused primarily by vestibular hair cell damage. J Neurosci Res 2010;88(6):1262-1272,
  • Sun G, Fujii M, Sonoda A, Tokumaru Y, Matsunaga T, Habu N Identification of stem-like cells in head and neck cancer cell lines. Anticancer Research 2010;30(6): 2005-2010
  • 松永達雄
    遺伝性難聴と遺伝カウンセリング
    In:小川郁・編集.　よくわかる聴覚障害―難聴と耳鳴のすべて―.　
    永井書店：東京　2010；344-348
  • 岡本康秀、松永達雄、泰地秀信、守本倫子、坂田英明、安達のどか、貫野彩子、山口聡子、仲野敦子、高木明、加我 君孝、小川郁
    前庭水管拡大症の確実例とボーダーライン例のSLC26A4遺伝子変異および臨床所見の特徴
    Audiology Japan 53 (2) 164 – 170, 2010
  • 泰地秀信、守本倫子、松永達雄
    Auditory neuropathy spectrum disorderの乳幼児期におけるASSR閾値
    Audiology Japan 53 (1),76-83, 2010
  • 松永達雄
    若い頃から難聴で補聴器を使っていますが、子どもに遺伝しますか？
    JOHNS：東京 26 (9) 1260 – 1261
  • 進藤彰人、松永達雄
    BPPV以外で、メニエール病、前庭神経炎、突発性難聴などの回転性めまいを生じる耳鼻科的疾患について、ジェネラリストが知っておくべきこと
    JIM 20 (12)  932 – 935, 2010
  • 松永達雄
    遺伝性感音難聴の研究
    オーディオインフォ 8 (2010) 17-19
  • 松永達雄（監修）
    平衡感覚を取り戻す人工内耳
    日経サイエンス：東京　2010年8月号(第40巻第8号) p80-84　日経サイエンス社　

2009

  • Mutai H, Nagashima R, Sugitani Y, Noda T, Fujii M, Matsunaga T. Expression of Pou3f3/Brn-1 and its genomic methylation in developing auditory epithelium. Dev Neurobiol 69 (14):913-930, 2009
  • Mutai H, Nagashima R, Fujii M, Matsunaga T. Mitotic activity and specification of fibrocytes subtypes in the developing rat cochlear lateral wall. Neuroscience 163 (4):1255-1263, 2009
  • Matsunaga T
    Value of genetic testing in the otological approach for sensorineural hearing loss.
    Keio J Med 2009; 58(4): 216-222
  • Kunishima S, Matsunaga T, Ito Y, Saito H Mutations in MYH9 exons 1, 16, and 30 are infrequently found in Japanese patients with nonsyndromic deafness. Genet Test Mol Biomarkers 2009; 13(5): 705-707
  • Matsunaga T
    Trends in genetic research on auditory neuropathy.
    In: Neuropathies of the Auditory and Vestibular Eighth Cranial Nerves. Kaga K, Starr A (Eds). Springer, London. 2009；43-50
  • Ozawa H, Mutai H, Matsunaga T, Tokumaru Y, Fujii M, Sakamoto K, Tomita T, Ogawa K. Promoted cell proliferation by connexin 30 gene transfection to head-and-neck cancer cell line Anticancer Res 2009 29(6):1981-1985, 2009
  • 松永達雄
    中等度難聴の遺伝子
    In：加我君孝、内山勉、新正由紀子・編.　小児の中等度難聴ハンドブック.　
    金原出版：東京　2009；51-57
  • 松永達雄、孫こうい、務台英樹
    病因と遺伝子
    In：朝戸裕貴、加我君孝・編.　小耳症・外耳道閉鎖症に対する機能と形態の再建.
    金原出版：東京　2009；11-16
  • 松永達雄
    薬剤性聴覚障害の発症予防のための12SribosomalRNAミトコンドリア遺伝子変異解析
    臨床薬理の進歩　2009;30:21-26
  • 加我君孝、竹腰英樹、松永達雄、朝戸裕貴
    小耳症・外耳道閉鎖 In:日本小児耳鼻咽喉科学会・編.　小児耳鼻咽喉科診療指針.　
    金原出版：東京　2009;101-113
  • 加我君孝、竹腰英樹、新正由紀子、松永達雄
    幼小児の人工内耳手術　-先天性および後天性高度難聴児に聴覚を回復させる新しい医療-
    Bio Industry 2009;26(3):92-98
  • 矢島陽子、徳丸裕、羽生昇、松永達雄、藤井正人、大島久二
    呼吸困難を主訴とした再発性多発軟骨炎例
    耳鼻臨床　2009;102：4；309-313,
  • 徳丸裕、藤井正人、羽生昇、矢島陽子、松永達雄、角田晃一、加我君孝
    頭頚部扁平上皮癌におけるヒト乳頭腫ウイルス（HPV）の感染とp53遺伝子変異
    頭頚部癌：東京 35(4):360-364, 2009
  • 松永達雄
    突然聞こえなくなったら　 診察室　心と体　
    日経ビジネス：東京　2009年10月19日発行p66
  • 松永達雄
    両耳の高度難聴者への人工内耳手術とリハビリ
    医心伝心
    週刊ポスト：東京　2009年5月15日号p73

2008

  • Mizutari K, Tsunoda K, Matsunaga T, Masuda K, Fujii R, Fujii M. Oropharyngeal tuberculosis Intern Med J 2008;38(6):449-450
  • Mizutari K, Matsunaga T, Kamiya K, Fujinami Y, Fujii M, Ogawa K. Caspase inhibitor facilitaes recovery of hearing by protecting the cochlear lateral wall from acute cochlear mitochondrial dysfunction. J Neurosci Res 86; 215-222: 2008
  • 松永達雄
    蝸牛線維細胞を標的とした感音難聴の再生治療
    医学のあゆみ：東京　2008;226(11):986-990
  • 松永達雄
    小児難聴の遺伝子診断の実際
    小児耳鼻咽喉科：東京　2008;29(3):284-286
  • 松永達雄、務台英樹
    Auditory Neuropathyの遺伝子研究の動向
    MB ENT 2008;93:11-16
  • 松永達雄
    薬剤性難聴
    In：服部光男、岡島重孝・総監修.　新版　家庭医学大事典.　小学館：東京　2008；1141
  • 松永達雄
    遺伝性難聴
    In：服部光男、岡島重孝・総監修.　新版　家庭医学大事典.　 小学館：東京　2008；1141
  • 松永達雄
    難聴の遺伝
    小児内科：東京 2008;40(8)1354-1358
  • 松永達雄、幸池浩子、務台英樹
    難聴の遺伝子検査
    神経内科：東京　68(5) 415-421,2008
  • 松永達雄
    先天性難聴と遺伝子スクリーニング
    医療62(2)104-108,2008

2007

  • Kamiya K, Fujinami Y, Hoya N, Okamoto Y, Kouike H, Komatsuzaki R, Kusano R, Nakagawa S, Satoh H, Fujii M, Matsunaga T. Mesenchymal stem cell transplantation accelerates hearing recovery through the repair of injured cochlear fibrocytes. Am J Pathol 171(1) 214-226; 2007（Press released by Am J Pathol as “Can you hear me now? Stem cells enhance hearing recovery” on June 25, 2007 at “EurekAlert!”.）
  • Matsunaga T, Okada M, Usami S, Okuyama T. Phenotypic consequences in a Japanese family having branchio-oto-renal syndrome with a novel frameshift mutation in the gene EYA1. Acta Otolaryngologica 127; 98-104: 2007
  • Ozawa H, Matsunaga T, Kamiya K, Tokumaru Y, Fujii M, Tomita T, Ogawa K. Decreased expression of connexin-30 and aberrant expression of connexin-26 in human head and neck cancer. Anticancer Res 27(4B); 2189 – 2195: 2007
  • 藤井正人、徳丸裕、羽生昇、矢島陽子、松永達雄、角田晃一、萬篤憲
    Salvage手術　-化学放射線療法後の頚部郭清術-
    頭頚部癌 2007;33(3):352-355.

2006

  • Matsunaga T, Hirota E, Bito S, Niimi S, Usami SI. Clinical Course of Hearing and Language Development in GJB2 and Non-GJB2 Deafness following Habilitation with Hearing Aids. Audiol Neurootol. 2006,11(1):59-68
  • Ozawa H, Fujii M, Matsunaga T, Masuda K, Hirose S, Taiji H. Oncocytic carcinoma of the parotid gland. Journal of Otolaryngology 35 (3)  189 – 192; 2006
  • 松永達雄
    難聴の遺伝相談とその言語聴覚リハビリテーションへの応用
    Audiology Japan 2006, 49 (4)  339 – 345
  • 松永達雄
    メニエール病と蝸牛線維細胞障害
    Equibrium Res. 65(2)129, 2006.
  • 神崎仁、佐藤美奈子、松永達雄、熊埜御堂浩、神崎晶、小川郁
    突発性難聴の可逆性について
    Audiology Japan 2006, 49 (6)  782 – 788

2005

  • Matsunaga T, Kumanomido H, Shiroma M, Goto Y, Usami S. Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycoside. Ann Otol Rhinol Laryngol, 114, 2, 153-160, 2005.
  • Okamoto Y, Hoya N, Kamiya K, Fujii M, Ogawa K, Matsunaga T. Permanent threshold shift caused by acute cochlear mitochondrial dysfunction is primarily mediated by degeneration of the lateral wall of the cochlea. Audiol Neurootol, 10, 4, 220-233, 2005.
  • Oguchi T, Ohtsuka A, Hashimoto S, Oshima A, Abe S, Kobayashi Y, Nagai K, Matsunaga T, Iwasaki S, Nakagawa T, Usami S. Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns. J Human Genet, 50, 2, 76-83, 2005.
  • Masuda K, Ozawa H, Fujii M, Kimura S, Nagasaki K, Matsunaga T, Tsunoda K. Critical spontaneous rupture of a common carotid artery pseudo-aneurysm. Lancet 366, 2034, 2005.
  • Ozawa H, Kimura S, Mizutari K, Fujimine T, Fujii M, Ikeuchi S, Matsunaga T, Tsunoda K. Aphonia and dysphagia after total gastrectomy. Acta Otolaryngol (Stockh) 2005, 125:1244-1246.
  • Matsunaga T, Kamiya K, Okamoto Y, Hoya N, Mizutari K, Fujinami Y, Fujii M. 2005. Degeneration and regeneration of cochlear fibrocytes mediate hearing loss and its recovery in a model of acute cochlear mitochondrial dysfunction. In Proceedings of the Fifth International Symposium. Meniere’s disease & Inner Ear Homeostasis Disorders. David J. Lim, editor. House Ear Institute. Los Angels, California, USA. 250-251.
  • 神崎仁、松永達雄
    突発性難聴-最近の話題
    日医雑誌：東京　134巻　8号、1504-1508、2005.
  • 藤井正人、松永達雄、角田晃一、水足邦雄、藤井良一、増田圭奈子、木村聡子、富田俊樹、小沢宏之、藤峰武克
    下咽頭癌の治療戦略
    頭頚部癌：東京　31(3) 363-368, 2005

2004

  • Matsunaga T, Kumanomido H, Shiroma M, Ohtsuka A, Asamura K, Usami S. Deafness due to A1555G mitochondrial mutation without use of aminoglycoside. Laryngoscope 114, 6, 1085-1091, 2004.
  • Hoya N, Okamoto Y, Kamiya K, Fujii M, Matsunaga T. A novel animal model of acute cochlear mitochondrial dysfunction: Model of cochlear mitochondrial dysfunction. Neuroreport 15, 10, 1597-1600, 2004.
  • Niizeki H, Matsunaga T, Iwata T, Shimizu T, Kurimoto I, Naruse T, Inoko H, Streilein JW. The MICA5.1 allele is not associated with susceptibility to effects of ultraviolet-B radiation on induction of contact hypersensitivity. J Dermatol Sci 35, 3, 221-223, 2004.
  • 松永達雄
    難聴遺伝子研究の現況と展望
    医療, 58, 9, 510-514, 2004.
  • 城間将江、松永達雄
    人工内耳装用者の聴取に関する考察
    医療, 58, 9, 522-527, 2004.
  • 藤井正人、小沢宏之、松永達雄、増田圭奈子、水足邦雄、木村聡子、角田晃一、冨田俊樹、山口寛、田川崇正
    頭頚部癌未治療例に対するドセタキセル、シスプラチン、5-FU併用療法の検討
    癌の臨床：東京 50, 10, 837-841, 2004.
  • 藤井正人、小沢宏之、松永達雄、増田圭奈子、水足邦雄、冨田俊樹、山口寛、田川崇正
    頭頚部癌に対するドセタキセル、シスプラチン、TS-1併用療法の検討
    耳鼻, 50(補1):S14-18, 2004.

2003

  • Matsunaga T, Hirota E. Familial lateral semicircular canal malformation with external and middle ear abnormalities. Am J Med Genet 2003; 116A: 360-367
  • 松永達雄．
    止血薬．耳鼻咽喉科薬物療法マニュアル　In：神崎 仁、小川 郁 編． 金原出版 2003; 69-73.

2002

  • Yuge I, Ohtsuka A, Matsunaga T, Usami S. Identification of 605ins46, a novel GJB mutation in a Japanese family. Auris Nasus Larynx 2002; 29: 379-382

2001

  • Matsunaga T, Davis JG, Greene MI. Adult rat otic placode-derived neurons and sensory epithelium express all four erbB receptors: A role in regulating vestibular ganglion neuron viability. DNA Cell Biol 2001; 20: 307-320
  • 佐藤美奈子、松永達雄、神崎仁、小川郁、井上泰宏、保谷則之. 突発性難聴の重症度分類と予後との関係. 日耳鼻会報 2001; 104: 192-197
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