메뉴 건너뛰기




Volumn 123, Issue 6, 1997, Pages 573-577

Inherited nonsyndromic hearing loss: An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; AUDIOGRAPHY; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 1P; FAMILY HISTORY; FEMALE; GENE LOCATION; GENETIC LINKAGE; HUMAN; MAJOR CLINICAL STUDY; MALE; PEDIGREE ANALYSIS; PERCEPTION DEAFNESS;

EID: 0030917967     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.1997.01900060015002     Document Type: Article
Times cited : (44)

References (20)
  • 3
    • 0028101878 scopus 로고
    • Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families
    • Coucke P, Van Camp G, Djoyodiharjo B, et al. Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families. N Engl J Med. 1994;331:425-431.
    • (1994) N Engl J Med , vol.331 , pp. 425-431
    • Coucke, P.1    Van Camp, G.2    Djoyodiharjo, B.3
  • 5
    • 0031127215 scopus 로고    scopus 로고
    • Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25 Mb region on chromosome 1p
    • In press
    • van Camp G, Coucke PJ, Kunst D, et al. Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25 Mb region on chromosome 1p. Genomics. In press.
    • Genomics
    • Van Camp, G.1    Coucke, P.J.2    Kunst, D.3
  • 8
    • 0028227613 scopus 로고
    • Nonsyndromic hearing loss: An analysis of audiograms
    • Liu X, Xu L. Nonsyndromic hearing loss: an analysis of audiograms. Ann Otol Rhinol Laryngol. 1994;103:428-433.
    • (1994) Ann Otol Rhinol Laryngol , vol.103 , pp. 428-433
    • Liu, X.1    Xu, L.2
  • 9
    • 0000112325 scopus 로고
    • The aetiology of congenital deafness and audiometric patterns
    • Fisch L. The aetiology of congenital deafness and audiometric patterns. J Laryngol Otol. 1955;69:479-493.
    • (1955) J Laryngol Otol , vol.69 , pp. 479-493
    • Fisch, L.1
  • 11
    • 0018610799 scopus 로고
    • Nystagmometry: The art of measuring nystagmus parameters by digital signal processing
    • Huygen PLM. Nystagmometry: the art of measuring nystagmus parameters by digital signal processing. ORL J Otorhinolaryngol Relat Spec. 1979;41:206-220.
    • (1979) ORL J Otorhinolaryngol Relat Spec , vol.41 , pp. 206-220
    • Huygen, P.L.M.1
  • 12
    • 0021092858 scopus 로고
    • Vestibular hyperreactivity in patients with multiple sclerosis
    • Huygen PLM. Vestibular hyperreactivity in patients with multiple sclerosis. Adv Otorhinolaryngol. 1993;30:141-149.
    • (1993) Adv Otorhinolaryngol , vol.30 , pp. 141-149
    • Huygen, P.L.M.1
  • 13
    • 0026454907 scopus 로고
    • Oculomotor and vestibular anomalies in Pelizaeus-Merzbacher disease: A study on a kindred with 2 affected and 3 normal males, 3 obligate and 8 possible carriers
    • Huygen PLM, Verhagen WIM, Renier WO. Oculomotor and vestibular anomalies in Pelizaeus-Merzbacher disease: a study on a kindred with 2 affected and 3 normal males, 3 obligate and 8 possible carriers. J Neurol Sci. 1992;113: 17-25.
    • (1992) J Neurol Sci , vol.113 , pp. 17-25
    • Huygen, P.L.M.1    Verhagen, W.I.M.2    Renier, W.O.3
  • 15
    • 0026667822 scopus 로고
    • Oculomotor, auditory, and vestibular responses in myotonic dystrophy
    • Verhagen WIM, Ter Bruggen JP, Huygen PLM. Oculomotor, auditory, and vestibular responses in myotonic dystrophy. Arch Neurol. 1992;49:954-960.
    • (1992) Arch Neurol , vol.49 , pp. 954-960
    • Verhagen, W.I.M.1    Ter Bruggen, J.P.2    Huygen, P.L.M.3
  • 17
    • 0013862487 scopus 로고
    • Studies on progressive hereditary perceptive deafness in a family of 335 members
    • Huizing EH, Van Bolhuis AH, Odenthal W. Studies on progressive hereditary perceptive deafness in a family of 335 members. Acta Otolaryngol (Stockh). 1966;61:161-167.
    • (1966) Acta Otolaryngol (Stockh) , vol.61 , pp. 161-167
    • Huizing, E.H.1    Van Bolhuis, A.H.2    Odenthal, W.3
  • 18
    • 0028803173 scopus 로고
    • Localization of a gene for nonsyndromic hearing loss (DFNA5) to chromosome 7p15
    • Van Camp G, Coucke P, Balemans W, et al. Localization of a gene for nonsyndromic hearing loss (DFNA5) to chromosome 7p15. Hum Mol Genet. 1995; 4:2159-2163.
    • (1995) Hum Mol Genet , vol.4 , pp. 2159-2163
    • Van Camp, G.1    Coucke, P.2    Balemans, W.3
  • 19
    • 0016428299 scopus 로고
    • Vestibulo-ocular function in patients with cerebellar atrophy
    • Baloh RW, Konrad HR, Honrubia V. Vestibulo-ocular function in patients with cerebellar atrophy. Neurology. 1975;25:160-168.
    • (1975) Neurology , vol.25 , pp. 160-168
    • Baloh, R.W.1    Konrad, H.R.2    Honrubia, V.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.