Mitochondrial ribosome and Ménière’s disease: a pilot study-Reference-Cited by-同舟云学术

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Mitochondrial ribosome and Ménière’s disease: a pilot study

Published:2012-06-13 Issue:8 Volume:269 Page:2003-2008
ISSN:0937-4477
Container-title:European Archives of Oto-Rhino-Laryngology
language:en
Short-container-title:Eur Arch Otorhinolaryngol

Author:

Pacheu-Grau David,Pérez-Delgado Laura,Gómez-Díaz Covadonga,Fraile-Rodrigo Jesus,Montoya Julio,Ruiz-Pesini Eduardo

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Otorhinolaryngology

Link

http://link.springer.com/content/pdf/10.1007/s00405-012-2066-8.pdf

Reference22 articles.

1. Silverstein H, Wazen J, Van Ess MJ, Daugherty J, Alameda YA (2010) Intratympanic gentamicin treatment of patients with Meniere’s disease with normal hearing. Otolaryngol Head Neck Surg 142(4):570–575

2. Perez-Delgado L, Fraile-Rodrigo J, Astier-Peña P (2011) Intratympanic gentamicin in Ménière’s disease: our experience. J Laryngol Otol 125:363–369

3. Prezant TR, Agapian JV, Bohlman MC, Bu X, Oztas S, Qiu WQ, Arnos KS, Cortopassi GA, Jaber L, Rotter JI et al (1993) Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nat Genet 4(3):289–294

4. Zhao H, Li R, Wang Q, Yan Q, Deng JH, Han D, Bai Y, Young WY, Guan MX (2004) Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family. Am J Hum Genet 74(1):139–152

5. Vandebona H, Mitchell P, Manwaring N, Griffiths K, Gopinath B, Wang JJ, Sue CM (2009) Prevalence of mitochondrial 1555A → G mutation in adults of European descent. N Engl J Med 360(6):642–644

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