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Tag Archives: Usher Syndrome

Hope for the Hearing Impaired

Posted on March 31, 2010 by Ron Pavellas

I recently attended a public seminar at the renown Karolinska Institute in Stockholm: “Hereditary Hearing Impairment and Therapeutic Strategies”. The subject of hearing, and not hearing well, is important to me. I have worn a hearing aid in each ear … Continue reading →

Posted in Science & the Sciences, Technology | Tagged auditory brainstem response, auditory steady state responses, Örebro University, Claes Möller, cochlear implant, deafblind syndromes, DNA analysis, Electron micrograph of chromosomes, evoked otoacoustic emissions, genetic engineering, hearing, hearing aid, Hereditary Hearing Impairment and Therapeutic Strategies, Human Genome, Huntington's Disease, kanelbulle, Karolinska Institute, Lisbeth Tranebjærg, Lou Gehrig's Disease, mitochondrial mutations, Muscular Dystrophy, neonatal screening, Nobel Forum, non-syndromic deafness, nonsyndromic dominant gene, nonsyndromic recessive genes, Richard J. Smith, sign language, Syndromic Sensorineural Hearing Loss, University of Copenhagen, University of Iowa, Usher Syndrome, William J. Kimberling, x-linked gene | Leave a comment
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