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Informationen zum Autor Dafydd Stephens FRCP, is Honorary Professor of Audiological Medicine at Cardiff University, Wales, UK. Sophia E. Kramer, PhD, is Senior Researcher and Psychologist at the Department of E.N.T. / Audiology / EMGO Institute for Health and Care Research at the VU University Medical Centre in Amsterdam, the Netherlands. Klappentext This book comprises the first volume of a series which reports the outcomes of the European Union Concerted Action Programme on Genetic Hearing Impairment. The aim is to bring together clinical geneticists and audiologists, as well as basic scientists and other clinicians with a general interest in this field, to standardise the audiological and terminological approaches and publish state of the art interdisciplinary studies. Zusammenfassung Focuses on the results of gene localization and identification within the field and the development of more relevant audiometric and vestibulometric investigations. The book includes a review of gene localization and identification in non-syndromal autosomal recessive hearing impairment. Inhaltsverzeichnis Preface . Contributors. Part I Gene therapy. Chapter 1 Gene therapy for hearing disorders - AK Lalwani, GJ Carvalho, JJ Han and AN Mhatre. Part II Radiology. Chapter 2 Radiology of inner ear defects - PD Phelps. Part III Computer Systems Chapter 3 An Internet database on genetic non-syndromal hearing impairments - M. Mazzoli, L. Saggin, SD Hatzopouilos and A Martini. Chapter 4 A decision support system for the diagnosis of syndromal genetic hearing impairment - S Crino, A D'Amico, S Grisanti and G Grisanti. Part IV Epidemiology Chapter 5 Epidemiology of hereditary hearing impairment in childhood - preliminary estimates from the European Union - A Parving, RJC Admiraal, F Apaydin, E Arslan, A Davis, O Dias, H Fortnum, G Grisanti, M Gross, M Hess, K Konradsson, G Lina-Granade, VE Newton, C O'Donovan, E Orzan, M Sorri, D Stephens, MD Tsakanikox, M Waagenaar and K Welzl-Müller. Chapter 6 The German Registry for Hearing Impairment in Children: preliminary results - A Cherechevskaia, A Costa, E Rosztok, M Hess and M Gross. Chapter 7 Recessive hearing impairment in two birth cohorts in western Sicily - G Grisanti, AM Amodeo, S Crino and E Martines. Chapter 8 Aetiology of hearing impairment in children borth in northern Finland ijn 1975-1979 and in 1985-1989 (Abstract) - E Maki-Torkko, P Lindholm, M Vayrynen and M Sorri. Part V Audiovestibular tests. Chapter 9 Audiometric criteria for linkage analysis in genetic hearing impairment - FL Wuyts, PH Van de Heyning an F Declau. Chapter 10 Audioscan notches in carriers of genetic hearing impairment - F Zhao, D Stephens, R Meredith and VE Newton. Chapter 11 Cochlear irregulatities in obligate carriers of recessive genetic hearing impairment and in control subjects - G Lina-Granade, M Kreiss, T Gelas, L Collet and A Morgon. Chapter 12 Three-dimensional video-oculography for the detection of genetic vestibular dysfunction at the level of the threee semicircular canals and the otoliths (Abstract) - FL Wuyts, PH Van de Heyning, H Kingma, L Bourmans and D Van Dyck. Part VI Non-syndromal autosomal recessive hearing impairment. Chapter 13 Homozygosity mapping applied to hereditary hearing impairment - localizing recessive deafness genes - RJH Smith, A Ramesh, CR Srikumari Srisailapathy, K Fukushima, S Wayne, A Chen, L Van Laer, J Ashley, RIZ Zbar, M Lovett and G Van Camp. Chapter 14 A Turkish kindred with autosomal recessive non-syndromal hearing impairment segregates DFNB9 (Abstract) - SM Leal, E Vitale, F Apaydin, Y Hu, C Barnwell, M Iber, T Kandogan, U Braendle, HP Zenner, M S...
