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Items: 1 to 20 of 137

1.

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

Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Suzuki H, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima T.

Free Radic Res. 2013 Jul;47(6-7):498-506. doi: 10.3109/10715762.2013.793319. Epub 2013 May 7.

PMID:
23560644
2.

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.

DNA Cell Biol. 2012 Oct;31(10):1555-62. Epub 2012 Aug 9.

3.

Polymorphisms in genes encoding aquaporins 4 and 5 and estrogen receptor α in patients with Ménière's disease and sudden sensorineural hearing loss.

Nishio N, Teranishi M, Uchida Y, Sugiura S, Ando F, Shimokata H, Sone M, Otake H, Kato K, Yoshida T, Tagaya M, Hibi T, Nakashima T.

Life Sci. 2013 Mar 21;92(10):541-6. doi: 10.1016/j.lfs.2013.01.019. Epub 2013 Jan 24.

PMID:
23352976
4.

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.

Int J Immunogenet. 2011 Jun;38(3):249-54. doi: 10.1111/j.1744-313X.2011.01004.x. Epub 2011 Mar 9.

PMID:
21385326
5.

Polymorphisms in genes involved in inflammatory pathways in patients with sudden sensorineural hearing loss.

Hiramatsu M, Teranishi M, Uchida Y, Nishio N, Suzuki H, Kato K, Otake H, Yoshida T, Tagaya M, Suzuki H, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima T.

J Neurogenet. 2012 Sep;26(3-4):387-96. doi: 10.3109/01677063.2011.652266. Epub 2012 Mar 5.

PMID:
22385075
6.

Impact of methionine synthase gene and methylenetetrahydrofolate reductase gene polymorphisms on the risk of sudden sensorineural hearing loss.

Gross M, Friedman G, Eliashar R, Koren-Morag N, Goldschmidt N, Atta IA, Ben-Yehuda A.

Audiol Neurootol. 2006;11(5):287-93. Epub 2006 Jun 14.

PMID:
16778415
7.

Association between polymorphisms in genes encoding methylenetetrahydrofolate reductase and the risk of Ménière's disease.

Huang Y, Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima T.

J Neurogenet. 2013 Jun;27(1-2):5-10. doi: 10.3109/01677063.2013.770510. Epub 2013 Mar 13.

PMID:
23484733
8.

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.

Laryngoscope. 2013 Nov;123(11):E59-65. doi: 10.1002/lary.24298. Epub 2013 Aug 5.

PMID:
23832707
9.

Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with sudden sensorineural hearing loss.

Uchida Y, Sugiura S, Ando F, Shimokata H, Nakashima T.

Laryngoscope. 2010 Apr;120(4):791-5. doi: 10.1002/lary.20809.

PMID:
20213658
10.

Contribution of 1425G/A polymorphism in protein kinase C-Eta (PRKCH) gene and brain white matter lesions to the risk of sudden sensorineural hearing loss in a Japanese nested case-control study.

Uchida Y, Sugiura S, Nakashima T, Ando F, Shimokata H.

J Neurogenet. 2011 Oct;25(3):82-7. doi: 10.3109/01677063.2011.591462. Epub 2011 Jul 14.

PMID:
21756056
11.

Intratympanic dexamethasone and hyaluronic acid in patients with low-frequency and Ménière's-associated sudden sensorineural hearing loss.

Selivanova OA, Gouveris H, Victor A, Amedee RG, Mann W.

Otol Neurotol. 2005 Sep;26(5):890-5.

PMID:
16151334
12.

Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes.

Nishio N, Teranishi M, Uchida Y, Sugiura S, Ando F, Shimokata H, Sone M, Otake H, Kato K, Yoshida T, Tagaya M, Hibi T, Nakashima T.

Gene. 2012 May 10;499(1):226-30. doi: 10.1016/j.gene.2012.02.027. Epub 2012 Mar 8.

PMID:
22426290
14.

Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.

Gázquez I, Moreno A, Requena T, Ohmen J, Santos-Perez S, Aran I, Soto-Varela A, Pérez-Garrigues H, López-Nevot A, Batuecas A, Friedman RA, López-Nevot MA, López-Escamez JA.

Eur Arch Otorhinolaryngol. 2013 Mar;270(4):1521-9. doi: 10.1007/s00405-012-2268-0. Epub 2012 Nov 21.

PMID:
23179933
15.

[Influence of the hearing loss level and auditory sensation curve type on click evoked SP/AP amplitude ratio in Menière's disease].

Wang Z, Shao X, Zhi B, Yan W, Lin Y.

Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2001 Oct;15(10):446-9. Chinese.

PMID:
12541688
16.

A case-control study on proinflammatory genetic polymorphisms on sudden sensorineural hearing loss.

Cadoni G, Gaetani E, Picciotti PM, Arzani D, Quarta M, Giannantonio S, Paludetti G, Boccia S.

Laryngoscope. 2015 Jan;125(1):E28-32. doi: 10.1002/lary.24743. Epub 2014 Oct 27.

PMID:
25345762
17.

Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.

Usami S, Takahashi K, Yuge I, Ohtsuka A, Namba A, Abe S, Fransen E, Patthy L, Otting G, Van Camp G.

Eur J Hum Genet. 2003 Oct;11(10):744-8.

18.

Lack of association between inherited thrombophilic risk factors and idiopathic sudden sensorineural hearing loss in Italian patients.

Cadoni G, Scipione S, Rocca B, Agostino S, La Greca C, Bonvissuto D, Paludetti G.

Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.

PMID:
16572609
19.

Proinflammatory cytokine IL-1 β polymorphisms in sudden sensorineural hearing loss.

Um JY, Jang CH, Kim HL, Cho YB, Park J, Lee SJ, Kim YB, Kim HJ, Ahn KS, Jang HJ, Lee SG, Lee H, Lee KM, Kim SJ, Hong SH.

Immunopharmacol Immunotoxicol. 2013 Feb;35(1):52-6. doi: 10.3109/08923973.2012.719523. Epub 2012 Sep 26.

PMID:
23013363
20.

Glutathione s-transferase gene polymorphisms in Italian patients with sudden sensorineural hearing loss.

Cadoni G, Boccia S, Scipione S, Arzani D, Cianfagna F, Ricciardi G, Paludetti G, Agostino S.

Otol Neurotol. 2006 Dec;27(8):1166-9.

PMID:
16788422
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