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Free Radical Research Volume 47, 2013 - Issue 6-7
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Research Article

Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Ménière's disease

Masaaki TeranishiDepartment of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, JapanCorrespondence[email protected]
,
Yasue UchidaDepartment of Otorhinolaryngology, National Center for Geriatrics and Gerontology, Aichi, Japan;Department of Otolaryngology, Aichi Medical University, Aichi, Japan
,
Naoki NishioDepartment of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, Japan
,
Ken KatoDepartment of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, Japan
,
Hironao OtakeDepartment of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, Japan
,
Tadao YoshidaDepartment of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, Japan
,
Hirokazu SuzukiDepartment of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, Japan
,
Michihiko SoneDepartment of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, Japan
,
Saiko SugiuraDepartment of Otorhinolaryngology, National Center for Geriatrics and Gerontology, Aichi, Japan
,
Fujiko AndoDepartment for Development of Preventive Medicine, Center for Development of Advanced Medicine for Dementia (CAMD), National Center for Geriatrics and Gerontology, Aichi, Japan;Department of Health and Medical Sciences, Aichi Shukutoku University, Aichi, Japan
,
Hiroshi ShimokataDepartment for Development of Preventive Medicine, Center for Development of Advanced Medicine for Dementia (CAMD), National Center for Geriatrics and Gerontology, Aichi, Japan
&
Tsutomu NakashimaDepartment of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, Japan
 show all
Pages 498-506 | Received 22 Feb 2013, Accepted 04 Apr 2013, Published online: 07 May 2013

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Nasrin Yazdani, Armita Kakavand Hamidi, Negin Soroush, Neda Jalili, Aida Vahidi, Nakisa Zarabi Ahrabi, Ardavan Tajdini & Mahsa Amoli. (2018) eNOS gene Glu298Asp variant confer risk in sudden sensorineural hearing loss. Acta Oto-Laryngologica 138:10, pages 904-908.
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Ryosuke Kitoh, Shin-Ya Nishio & Shin-Ichi Usami. (2017) Prognostic impact of gene polymorphisms in patients with idiopathic sudden sensorineural hearing loss. Acta Oto-Laryngologica 137:sup565, pages S24-S29.
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Articles from other publishers (14)

Qingqing Dai, Lili Long, Hui Zhao, Ruikai Wang, Hong Zheng & Maoli Duan. (2022) Genetic advances in Meniere Disease. Molecular Biology Reports 50:3, pages 2901-2908.
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T. Requena, A. Keder, P. zur Lage, J. T. Albert & A. P. Jarman. (2022) A Drosophila model for Meniere’s disease: Dystrobrevin is required for support cell function in hearing and proprioception. Frontiers in Cell and Developmental Biology 10.
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Shoujun Gu, Rafal Olszewski, Lacey Nelson, Alvaro Gallego-Martinez, Jose Antonio Lopez-Escamez & Michael Hoa. (2021) Identification of Potential Meniere's Disease Targets in the Adult Stria Vascularis. Frontiers in Neurology 12.
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Armine Kocharyan, Michelle E. Mark, Mustafa S. Ascha, Gail S. Murray, Nauman F. Manzoor, Cliff Megerian, Sarah E. Mowry & Maroun T. Semaan. (2020) Cochlear Implantation in Patients With Menière's Disease: Does Disease Activity Affect the Outcome?. Otology & Neurotology 41:9, pages 1296-1304.
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Eun Hye Oh, Jin-Hong Shin, Hyang-Sook Kim, Jae Wook Cho, Seo Young Choi, Kwang-Dong Choi, Je-Keun Rhee, Seowhang Lee, Changwook Lee & Jae-Hwan Choi. (2020) Rare Variants of Putative Candidate Genes Associated With Sporadic Meniere's Disease in East Asian Population. Frontiers in Neurology 10.
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Zaizai Cao, Jinjian Gao, Saiyu Huang, Haijie Xiang, Chuqin Zhang, Bo Zheng, Xiang Zhan, Ruru Chen & Bobei Chen. (2019) Genetic Polymorphisms and Susceptibility to Sudden Sensorineural Hearing Loss: A Systematic Review. Audiology and Neurotology 24:1, pages 8-19.
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Janet L. Fitzakerley & George J. Trachte. (2018) Genetics of guanylyl cyclase pathways in the cochlea and their influence on hearing. Physiological Genomics 50:9, pages 780-806.
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Y Sun, D Zhang, G Sun, Y Lv, Y Li, X Li, Y Song, J Li, Z Fan & H Wang. (2018) RNA-sequencing study of peripheral blood mononuclear cells in sporadic Ménière's disease patients: possible contribution of immunologic dysfunction to the development of this disorder. Clinical and Experimental Immunology 192:1, pages 33-45.
Crossref
Shazia Mirza & Sankalp Gokhale. 2017. Up to Date on Meniere's Disease. Up to Date on Meniere's Disease.
Gerald M. Haase & Kedar N. Prasad. (2016) Oxidative Damage and Inflammation Biomarkers. Otology & Neurotology 37:8, pages e303-e308.
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XIAOJIANG LIN, YAOSHU TENG, JINSHAN LAN, BENJUN HE, HUIJUAN SUN & FENGLIN XU. (2016) GRHL2 genetic polymorphisms may confer a protective effect against sudden sensorineural hearing loss. Molecular Medicine Reports 13:3, pages 2857-2863.
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N. V. Boiko & N. L. Kunel’skaya. (2016) The current problems related to Meniere’s disease. Vestnik otorinolaringologii 81:5, pages 89.
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Takashi Anzai, Ichiro Fukunaga, Kaori Hatakeyama, Ayumi Fujimoto, Kazuma Kobayashi, Atena Nishikawa, Toru Aoki, Tetsuo Noda, Osamu Minowa, Katsuhisa Ikeda & Kazusaku Kamiya. (2015) Deformation of the Outer Hair Cells and the Accumulation of Caveolin-2 in Connexin 26 Deficient Mice. PLOS ONE 10:10, pages e0141258.
Crossref
Alessandro Castiglione, Andrea Ciorba, Claudia Aimoni, Elisa Orioli, Giulia Zeri, Marco Vigliano & Donato Gemmati. (2015) Sudden Sensorineural Hearing Loss and Polymorphisms in Iron Homeostasis Genes: New Insights from a Case-Control Study. BioMed Research International 2015, pages 1-10.
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