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Audiology Volume 34, 1995 - Issue 2
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Original Article

Application of the Audioscan in the Detection of Carriers of Genetic Hearing Loss

Original Paper

Dafydd Stephens Welsh Hearing Institute, University Hospital of Wales, Cardiff, UK
,
Rhys Meredith Welsh Hearing Institute, University Hospital of Wales, Cardiff, UK
,
Tony Sirimanna Welsh Hearing Institute, University Hospital of Wales, Cardiff, UK
,
Liz France Welsh Hearing Institute, University Hospital of Wales, Cardiff, UK
,
Charlotte Almqvist University of Lund School of Medicine, Lund, Sweden
&
Hedda Haugen University of Lund School of Medicine, Lund, Sweden
Pages 91-97 | Received 09 Nov 1994, Accepted 06 Apr 1995, Published online: 07 Jul 2009

Citations (13)

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Read on this site (10)

. (2016) Guidelines for aetiological investigation into unilateral permanent childhood hearing impairment. Hearing, Balance and Communication 14:3, pages 146-155.
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. (2016) Guidelines for aetiological investigation into severe to profound bilateral permanent childhood hearing impairment. Hearing, Balance and Communication 14:3, pages 135-145.
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. (2016) Guidelines for aetiological investigation into mild to moderate bilateral permanent childhood hearing impairment. Hearing, Balance and Communication 14:3, pages 125-134.
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Wan S. Ishak, Fei Zhao, Dafydd Stephens, John Culling, Zhong Bai & Christian Meyer-Bisch. (2011) Test-retest reliability and validity of Audioscan and Békésy compared with pure tone audiometry. Audiological Medicine 9:1, pages 40-46.
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Fei Zhao & Dafydd Stephens. (2007) A critical review of King-Kopetzky syndrome: Hearing difficulties, but normal hearing?. Audiological Medicine 5:2, pages 119-124.
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Adam Beckman, Gerald S. Conway & Barbara Cadge. (2004) Audiological features of Turner's syndrome in adults. International Journal of Audiology 43:9, pages 533-544.
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Fei Zhao, Dafydd Stephens. (1999) Audioscan Testing in Patients with King-Kopetzky Syndrome. Acta Oto-Laryngologica 119:3, pages 306-310.
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Fei Zhao & Dafydd Stephens. (1998) Analyses of Notches in Audioscan and DPOAEs in Subjects with Normal Hearing. Audiology 37:6, pages 335-343.
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M. Cohen, M. Francis, R. Coffey, M. E. Pembrey & L. M. Luxon. (1997) Abnormal Audiograms and Elevated Acoustic Reflex Thresholds in Obligate Carriers of Autosomal Recessive Non-Syndromic Hearing Loss. Acta Oto-Laryngologica 117:3, pages 337-342.
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M. Cohen, M. Francis, L. M. Luxon, S. Bellman, R. Coffey & M. Pembrey. (1996) Dips on Békésy or Audioscan Fail to Identify Carriers of Autosomal Recessive Non-Syndromic Hearing Loss. Acta Oto-Laryngologica 116:4, pages 521-527.
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Articles from other publishers (3)

Annamaria Franzé, Antonella Caravelli, Francesca Leva, Elio Marciano, Gennaro Auletta, Federica D’Aulos, Claudio Saulino, Laura Esposito, Massimo Carella & Paolo Gasparini. (2005) Audiometric evaluation of carriers of the connexin 26 mutation 35delG. European Archives of Oto-Rhino-Laryngology 262:11, pages 921-924.
Crossref
F. ZHAO, D. STEPHENS & C. MEYER-BISCH. (2002) The Audioscan: a high frequency resolution audiometric technique and its clinical applications. Clinical Otolaryngology and Allied Sciences 27:1, pages 4-10.
Crossref
Sandrine Marlin, Françoise Denoyelle, Denise Busquet, Noël Garabedian & Christine Petit. (1998) A particular case of deafness-oligodontia syndrome. International Journal of Pediatric Otorhinolaryngology 44:1, pages 63-69.
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