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ORIGINAL ARTICLE

Aquaporin-2 and -4: Single nucleotide polymorphisms in Ménière's disease patients

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Pages 18-23 | Accepted 14 Dec 2009, Published online: 03 Feb 2010

References

  • Monsell EM, Balkany TA, Gates GA, Goldenberg RA, Meyerhoff WL, House JW. Committee on hearing and equilibrium guidelines for the diagnosis and evaluation of therapy in Ménière's disease. Otolaryngol Head Neck Surg. 1995; 113:181–5.
  • Merchant SN, Adams JC, Nadol JB Jr. Pathophysiology of Ménière's syndrome: are symptoms caused by endolymphatic hydrops? Am J Otol. 2005;26:74–81.
  • Shinomori Y, Kimura RS, Adams JC. Changes in immunos-taining for Na+, K+, 2Cl– cotransporter 1, taurine and c-Jun N-terminal kinase in experimentally induced endolymphatic hydrops. Assoc Res Otolaryngol Abs. 2001;24:134.
  • Kariya S, Cureoglu S, Fukushima H, Kusynoki T, Schachern PA, Nishizaki K, . Histopathologic changes of contralateral human temporal bone in unilateral Ménière's disease. Otol Neurotol. 2007;28:1063–8.
  • Paparella MM, Djalilian HR. Etiology, pathophysiology of symptoms and pathogenesis of Ménière's disease. Otolaryngol Clin N Am. 2002;35:529–45.
  • Klockars T, Kentala E. Inheritance of Ménière's disease in the Finnish population. Arch Otolaryngol Head Neck Surg. 2007;133:73–7.
  • Frykholm C, Larsen HC, Dahl N, Klar J, Rask-Andersen H, Friberg U. Familial Ménière's disease in five generations. Otol Neurotol. 2006;27:681–6.
  • Lalwani AK, Jackler RK, Sweetow RW, Lynch ED, Raventos H, Morrow J, . Further characterization of the DFNA1 audiovestibular phenotype. Arch Otolaryngol Head Neck Surg. 1998;124:699–702.
  • Robertson NG, Hamaker SA, Patriub V, Aster JC, Morton CC, . Subcellular localization, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9. J Med Gen. 2003;40:479–86.
  • Cryns K, Phister M, Pennings RJ, Bom SJ, Flothmann K, Caethoven G, . Mutations in the WFS1 gene that cause low frequency sensorineural hearing loss are small non-inactivating mutations. Hum Gen. 2002;110:389–94.
  • Okafor BC. Incidence of Ménière's disease. J Laryngol Otol. 1984;98:775–9.
  • Ibekwe TS, Ijaduola GT. Ménière's disease: rare or under-diagnosed among Africans. Eur Arch Otorhinolaryngol. 2007;264:1399–403.
  • Mhatre AN, Jero J, Chiappini I, Bolasco G, Barbara M, Lalwani K. Aquaporin-2 expression in the mammalian cochlea and investigation of its role in Ménière's disease. Hear Res. 2002;170:59–69.
  • Takeda T, Takeda S, Kitano H, Okada T, Kakigi A. Endolym-phatic hydrops induced by chronic administration of vaso-pressin. Hear Res. 2000;140:1–6.
  • Mhatre AN, Stern RE, Li J, Lalwani AK. Aquaporin-4 expression in the mammalian inner ear and its role in hearing. Bio-chem Biophys Res Commun. 2002;297:987–96.
  • Ishiyama G, Lopez IA, Ishiyama A. Aquaporins and Ménière's disease. Curr Opin Otolaryngol Head Neck Surg. 2006;14:332–6.
  • Christensen N, D’Souza M, Zhu X, Frisina RD. Age related hearing loss: aquaporin-4 gene expression changes in the mouse cochlea and auditory midbrain. Brain Res. 2009;1253:27–34.
  • Havia M, Kentala E, Pykko I. Prevalence of Ménière's disease in the general population of southern Finland. Otolaryngol Head Neck Surg. 2005;133:763–8.
  • Radtke A, von Brevern M, Feldmann M, Lezius F, Ziese T, Lempert T, . Screening for Ménière's disease in the general population – the needle in the haystack. Acta Oto-Laryngol. 2008;128:272–6.
  • Watanabe Y, Mizukoshi K, Shojaku H, Watanbe I, Hinoki M, Kitahara M. Epidemiological and clinical characteristics of Ménière's disease in Japan. Acta Otolaryngol Suppl. 1995;519:206–10.
  • Morrison AW, Bailey MES, Morrison GAJ. Familial Ménière's disease: clinical and genetic aspects. J Laryngol Otol. 2009;123:29–37.

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