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Vestibular aqueduct in sudden sensorineural hearing loss.
Sugiura M, Naganawa S, Ishida IM, Teranishi M, Nakata S, Yoshida T, Nakashima T. Sugiura M, et al. Among authors: yoshida t. J Laryngol Otol. 2008 Sep;122(9):887-92. doi: 10.1017/S0022215107000941. Epub 2007 Nov 26. J Laryngol Otol. 2008. PMID: 18036279
Association of interleukin-1 gene polymorphisms with sudden sensorineural hearing loss and Ménière's disease.
Furuta T, Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Tagaya M, Suzuki H, Sugiura M, Sone M, Hiramatsu M, Sugiura S, Ando F, Shimokata H, Nakashima T. Furuta T, et al. Among authors: yoshida t. Int J Immunogenet. 2011 Jun;38(3):249-54. doi: 10.1111/j.1744-313X.2011.01004.x. Epub 2011 Mar 9. Int J Immunogenet. 2011. PMID: 21385326
Polymorphisms in genes involved in oxidative stress response in patients with sudden sensorineural hearing loss and Ménière's disease in a Japanese population.
Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Suzuki H, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima T. Teranishi M, et al. Among authors: yoshida t. DNA Cell Biol. 2012 Oct;31(10):1555-62. doi: 10.1089/dna.2012.1631. Epub 2012 Aug 9. DNA Cell Biol. 2012. PMID: 22877234 Free PMC article.
Endothelin-1 gene polymorphism in sudden sensorineural hearing loss.
Uchida Y, Teranishi M, Nishio N, Sugiura S, Hiramatsu M, Suzuki H, Kato K, Otake H, Yoshida T, Tagaya M, Suzuki H, Sone M, Ando F, Shimokata H, Nakashima T. Uchida Y, et al. Among authors: yoshida t. Laryngoscope. 2013 Nov;123(11):E59-65. doi: 10.1002/lary.24298. Epub 2013 Aug 5. Laryngoscope. 2013. PMID: 23832707
Idiopathic sudden sensorineural hearing loss in Japan.
Nakashima T, Sato H, Gyo K, Hato N, Yoshida T, Shimono M, Teranishi M, Sone M, Fukunaga Y, Kobashi G, Takahashi K, Matsui S, Ogawa K. Nakashima T, et al. Among authors: yoshida t. Acta Otolaryngol. 2014 Nov;134(11):1158-63. doi: 10.3109/00016489.2014.919406. Acta Otolaryngol. 2014. PMID: 25315915 Free PMC article.
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