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Volumn 127, Issue 9, 2001, Pages 1045-1048

Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUDIOMETRY; CLINICAL ARTICLE; FEMALE; GENE; GENE DFNA2; GENE DFNA9; GENE LOCUS; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; MALE; PHONEME; PURE TONE AUDIOMETRY; SCORING SYSTEM; SPEECH DISCRIMINATION;

EID: 17944382920     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.127.9.1045     Document Type: Article
Times cited : (39)

References (14)
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    • Inherited nonsyndromic hearing loss: An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2
    • Marres H, van Ewijk M, Huygen P, et al. Inherited nonsyndromic hearing loss: an audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2. Arch Otolaryngol Head Neck Surg. 1997;123: 573-577.
    • (1997) Arch Otolaryngol Head Neck Surg. , vol.123 , pp. 573-577
    • Marres, H.1    Van Ewijk, M.2    Huygen, P.3
  • 3
    • 0031962461 scopus 로고
    • Nonsyndromic autosomal dominant progressive sensorineural hearing loss: Audiologic analysis of a pedigree linked to DFNA2
    • Kunst H, Marres H, Huygen P, et al. Nonsyndromic autosomal dominant progressive sensorineural hearing loss: audiologic analysis of a pedigree linked to DFNA2. Laryngoscope. 1993;108:74-80.
    • (1993) Laryngoscope , vol.108 , pp. 74-80
    • Kunst, H.1    Marres, H.2    Huygen, P.3
  • 6
    • 0032886813 scopus 로고    scopus 로고
    • Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9
    • Bom SJH, Kemperman MH, De Kok YJM, et al. Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9. Laryngoscope. 1999;109:1525-1530.
    • (1999) Laryngoscope , vol.109 , pp. 1525-1530
    • Bom, S.J.H.1    Kemperman, M.H.2    De Kok, Y.J.M.3
  • 10
    • 0026439315 scopus 로고
    • A new autosomal dominant syndrome of idiopathic progressive vestibulo-cochlear dysfunction with middle-age onset
    • Verhagen WIM, Huygen PLM, Bles W. A new autosomal dominant syndrome of idiopathic progressive vestibulo-cochlear dysfunction with middle-age onset. Acta Otolaryngol (Stockh). 1992;112:899-906.
    • (1992) Acta Otolaryngol (Stockh). , vol.112 , pp. 899-906
    • Verhagen, W.I.M.1    Huygen, P.L.M.2    Bles, W.3
  • 12
    • 0032837049 scopus 로고    scopus 로고
    • High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene
    • Fransen E, Verstreken M, Verhagen WIM, et al. High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene. Hum Mol Genet. 1999;8:1425-1429.
    • (1999) Hum Mol Genet. , vol.8 , pp. 1425-1429
    • Fransen, E.1    Verstreken, M.2    Verhagen, W.I.M.3
  • 13
    • 33847573569 scopus 로고    scopus 로고
    • Progressive late-onset sensorineural hearing loss and vestibular impairment with vertigo
    • In press
    • Lemaire FX, Feenstra L, Huygen PL, et al. Progressive late-onset sensorineural hearing loss and vestibular impairment with vertigo. Otol Neurotol. In press.
    • Otol Neurotol.
    • Lemaire, F.X.1    Feenstra, L.2    Huygen, P.L.3
  • 14
    • 0001622521 scopus 로고    scopus 로고
    • Autosomal-dominant progressive sensorineural hearing loss in a large North American family
    • March
    • Halpin C, Khetarpal U, McKenna M. Autosomal-dominant progressive sensorineural hearing loss in a large North American family. Am J Audiol. March 1996; 5:105-111.
    • (1996) Am J Audiol. , vol.5 , pp. 105-111
    • Halpin, C.1    Khetarpal, U.2    McKenna, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.