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Journal of Neurogenetics Volume 27, 2013 - Issue 1-2
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Research Article

Association Between Polymorphisms in Genes Encoding Methylenetetrahydrofolate Reductase and the Risk of Ménière's Disease

Yang HuangDepartment of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, Japan;Department of Otorhinolaryngology, The first People's Hospital of YunNan Province, Kun Ming, Yun Nan, China
,
Masaaki TeranishiDepartment of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, JapanCorrespondence[email protected]
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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
,
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 of Health and Medical Sciences, Aichi Shukutoku University, Aichi, Japan;Department for Development of Preventive Medicine, Center for Development of Advanced Medicine for Dementia (CAMD), National Center for Geriatrics and Gerontology, Aichi, Japan
,
Hiroshi ShimokataDepartment of Health and Medical Sciences, Aichi Shukutoku University, Aichi, Japan
&
Tsutomu NakashimaDepartment of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, Japan
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Pages 5-10 | Received 16 Oct 2012, Accepted 22 Jan 2013, Published online: 13 Mar 2013

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Masaaki Teranishi, Yasue Uchida, Naoki Nishio, Ken Kato, Hironao Otake, Tadao Yoshida, Hirokazu Suzuki, Michihiko Sone, Saiko Sugiura, Fujiko Ando, Hiroshi Shimokata & Tsutomu Nakashima. (2013) Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Ménière's disease. Free Radical Research 47:6-7, pages 498-506.
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Articles from other publishers (5)

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.
Crossref
Helmut SchaafHelmut Schaaf. 2021. Morbus Menière. Morbus Menière 289 295 .
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.
Crossref
Hyun Jin Lee, Jeon Mi Lee, Dae Bo Shim, Jinsei Jung, Sang Hyun Kwak & Sung Huhn Kim. (2019) Is Early Progression to Bilateral Involvement in Menière's Disease a Poor Prognostic Indicator?. Otology & Neurotology 40:10, pages 1333-1338.
Crossref
Elina Hietikko, Jouko Kotimäki & Minna Männikkö. 2005. Encyclopedia of Life Sciences. Encyclopedia of Life Sciences.

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