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Scandinavian Audiology Volume 28, 1999 - Issue 1
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Research Article

Prevalence of hereditary hearing impairment in adults

Yukimi Sakihara Department of Audiology, Bispebjerg Hospital H:S, DK Copenhagen NV, Denmark
,
Birger Christensen Department of Audiology, Bispebjerg Hospital H:S, DK Copenhagen NV, Denmark
&
Agnete Parving Department of Audiology, Bispebjerg Hospital H:S, DK Copenhagen NV, Denmark
Pages 39-46 | Published online: 12 Oct 2009

Citations (11)

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Read on this site (3)

Susan D. Jacobsen, Karen Gronskov, Karen Brondum-Nielsen & Agnete Parving. (2001) Is there a relationship between U-shaped audiograms and mutations in Connexin 26?. Scandinavian Audiology 30:3, pages 184-188.
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Agnete Parving, Yukimi Sakihara & Birger Christensen. (2000) Inherited Sensorineural Low-Frequency Hearing Impairment: Some Aspects of Phenotype and Epidemiology. Audiology 39:1, pages 50-60.
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Erik Borg, Eva Samuelsson, N. Dahl. (2000) Audiometric Characterization of a Family with Digenic Autosomal, Dominant, Progressive Sensorineural Hearing Loss. Acta Oto-Laryngologica 120:1, pages 51-57.
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Articles from other publishers (8)

Omnia Elsayed & Aisha Al‐Shamsi. (2022) Mutation spectrum of non‐syndromic hearing loss in the UAE, a retrospective cohort study and literature review. Molecular Genetics & Genomic Medicine 10:11.
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Mariem Sidenna, Tasnim Fadl & Hatem Zayed. (2020) Genetic Epidemiology of Hearing Loss in the 22 Arab Countries: A Systematic Review. Otology & Neurotology 41:2, pages e152-e162.
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Eugenia Borgione, Mariangela Lo Giudice, Filippa Castello, Sebastiano A. Musumeci, Francesco D. Di Blasi, Maria Savio, Maurizio Elia, Biagio Rizzo, Giuliano Barbarino, Salvatore Romano, Giuseppe Calabrese, Daniela Di Benedetto & Carmela Scuderi. (2013) The 9-bp deletion in region V of mtDNA: a risk factor of hearing loss and encephalomyopathy in Caucasian populations?. Neurological Sciences 34:7, pages 1223-1226.
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Hideki Mutai, Hiroko Kouike, Eiko Teruya, Ikuko Takahashi-Kodomari, Hiroki Kakishima, Hidenobu Taiji, Shin-ichi Usami, Torayuki Okuyama & Tatsuo Matsunaga. (2011) Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation. BMC Medical Genetics 12:1.
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Laura A. Raynor, James S. Pankow, Michael B. Miller, Guan-Hua Huang, Dayna Dalton, Ronald Klein, Barbara E. K. Klein & Karen J. Cruickshanks. (2009) Familial Aggregation of Age-Related Hearing Loss in an Epidemiological Study of Older Adults. American Journal of Audiology 18:2, pages 114-118.
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Robert A. Dobie. (2008) The Burdens of Age-related and Occupational Noise-Induced Hearing Loss in the United States. Ear & Hearing 29:4, pages 565-577.
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Catherine M. McMahon, Annette Kifley, Elena Rochtchina, Philip Newall & Paul Mitchell. (2008) The Contribution of Family History to Hearing Loss in an Older Population. Ear & Hearing 29:4, pages 578-584.
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Reinhard Ramsebner, Trevor Lucas, Christian Schoefer, Martin Ludwig, Wolf-Dieter Baumgartner, Franz J. Wachtler, Karin Kirschhofer & Klemens Frei. (2007) Relevance of the A1555G Mutation in the 12S rRNA Gene for Hearing Impairment in Austria. Otology & Neurotology 28:7, pages 884-886.
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