메뉴 건너뛰기




Volumn 34, Issue 1, 2007, Pages 101-104

Case report: Meniere's disease and otosclerosis-Different outcomes of the same disease?

Author keywords

Genetics; Inheritance; Meniere's disease; Otosclerosis

Indexed keywords

BETAHISTINE; CHLORTALIDONE; CLONAZEPAM; FLUORIDE; GENTAMICIN; LIDOCAINE; UREA;

EID: 33846379292     PISSN: 03858146     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.anl.2006.09.020     Document Type: Article
Times cited : (7)

References (7)
  • 1
    • 0036620280 scopus 로고    scopus 로고
    • Genetics (molecular biology) and Meniere's disease
    • Morrison A.W., and Johnson K.J. Genetics (molecular biology) and Meniere's disease. Otolaryngol Clin North Am 35 (2002) 497-516
    • (2002) Otolaryngol Clin North Am , vol.35 , pp. 497-516
    • Morrison, A.W.1    Johnson, K.J.2
  • 4
    • 0037399444 scopus 로고    scopus 로고
    • The aetiology of otosclerosis: a review of the literature
    • Menger D.J., and Tange R.A. The aetiology of otosclerosis: a review of the literature. Clin Otolaryngol 28 (2003) 112-120
    • (2003) Clin Otolaryngol , vol.28 , pp. 112-120
    • Menger, D.J.1    Tange, R.A.2
  • 5
    • 0018236787 scopus 로고
    • Otosclerosis: vestibular symptoms and sensorineural hearing loss
    • Cody D.T., and Baker Jr. H.L. Otosclerosis: vestibular symptoms and sensorineural hearing loss. Ann Otol Rhinol Laryngol 87 (1978) 778-796
    • (1978) Ann Otol Rhinol Laryngol , vol.87 , pp. 778-796
    • Cody, D.T.1    Baker Jr., H.L.2
  • 6
    • 0025192569 scopus 로고
    • Meniere's symptoms resulting from bilateral otosclerotic occlusion of the endolymphatic duct: an analysis of a causal relationship between otosclerosis and Meniere's disease
    • Franklin D.J., Pollak A., and Fisch U. Meniere's symptoms resulting from bilateral otosclerotic occlusion of the endolymphatic duct: an analysis of a causal relationship between otosclerosis and Meniere's disease. Am J Otol 11 (1990) 135-140
    • (1990) Am J Otol , vol.11 , pp. 135-140
    • Franklin, D.J.1    Pollak, A.2    Fisch, U.3
  • 7
    • 17344363707 scopus 로고    scopus 로고
    • Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction
    • Robertson N.G., Lu L., Heller S., Merchant S.N., Eavey R.D., McKenna M., et al. Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction. Nat Genet 20 (1998) 299-303
    • (1998) Nat Genet , vol.20 , pp. 299-303
    • Robertson, N.G.1    Lu, L.2    Heller, S.3    Merchant, S.N.4    Eavey, R.D.5    McKenna, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.