Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Valerie Newton"'
Autor:
Valerie Newton
Publikováno v:
Hearing, Balance and Communication. 11:91-99
Newborn hearing screening has resulted in hearing loss being detected significantly earlier than previously. Research has shown that there are several areas in which this has changed the outcome for the child concerned and the family, and has indicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfde15b37a424753f9a67ef7d700618a
https://doi.org/10.3109/21695717.2013.820512
https://doi.org/10.3109/21695717.2013.820512
Autor:
Xiao Mei Ouyang, Steve D.M. Brown, Thomas J. Balkany, Denise Yan, Simon I. Angeli, Walter E. Nance, J. Fielding Hejtmancik, Xue Zhong Liu, An Ren Li, Li Lin Du, Valerie Newton, Samuel G. Jacobson, M. Kaiser
Publikováno v:
Human Genetics. 116:292-299
Usher syndrome type I (USH1), the most severe form of this syndrome, is characterized by profound congenital sensorineural deafness, vestibular dysfunction, and retinitis pigmentosa. At least seven USH1 loci, USH1A-G, have been mapped to the chromoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bae6358aea41e07636be543dbf7828e
https://doi.org/10.1007/s00439-004-1227-2
https://doi.org/10.1007/s00439-004-1227-2
Publikováno v:
Audiological Medicine. 2:229-236
Evoked otoacoustic emissions (EOAEs) are widely used as a neonatal hearing-screening tool. During the first postnatal days, marked changes in the characteristics of EOAEs have been reported in human neonates. These changes have been mainly attributed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aed7a07b4cd90a7129bc27cb17431b3a
https://doi.org/10.1080/16513860410000401
https://doi.org/10.1080/16513860410000401
Autor:
J. F. Hejtmancik, Xiaomei Ouyang, Walter E. Nance, L. L. Du, M. Kaiser, Samuel G. Jacobson, Thomas J. Balkany, Xia Juan Xia, A. R. Li, Valerie Newton, Xue Zhong Liu
Publikováno v:
Clinical Genetics. 63:150-153
Usher syndrome (USH) is characterized by the associated findings of hearing loss and retinitis pigmentosa (RP), leading to progressive loss of vision. Three forms of USH can be distinguished clinically. In the most severe form, USH1, profound congeni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78ded8b23e810a6a788bcad5eaa44d84
https://doi.org/10.1046/j.0009-9163.2002.00004.x
https://doi.org/10.1046/j.0009-9163.2002.00004.x
Autor:
Sue Butler, Julie Morris, Alistair Burns, Frances Hickson, N. Harry P. Allen, Richard Ramsden, Valerie Newton, Jenny Rogers, Gillian Thistlewaite
Publikováno v:
Age and Ageing. 32:189-193
Background: audiological function is impaired in people with dementia and poor hearing is known to exaggerate the effects of cognitive deficits. Objective: the objective of this study was to assess the effects of increasing auditory acuity by providi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::956ebc1602b72c2d4c18126d5b1bfcd5
https://doi.org/10.1093/ageing/32.2.189
https://doi.org/10.1093/ageing/32.2.189
Autor:
Valerie Newton
Publikováno v:
Seminars in Neonatology. 6:543-551
Epidemiological studies in a number of Western countries have attributed 6-14% of sensorineural hearing impairment from birth or early childhood to problems relating to the birth process [1-4]. In spite of this association it is not always clear in i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c24e1ffb10a8bb034b85d73b154ed1a
https://doi.org/10.1053/siny.2001.0076
https://doi.org/10.1053/siny.2001.0076
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 57:229-234
In developing countries, there is a lack of trained personnel and testing equipment to facilitate the early detection of hearing impairment in children. A questionnaire offers a low cost option and the value of this for detecting hearing impairment i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec347e328645ed1230bd318b9436dc93
https://doi.org/10.1016/s0165-5876(00)00453-5
https://doi.org/10.1016/s0165-5876(00)00453-5
Autor:
W. Neary, James E. Gillespie, R Macleod, J P R Jenkins, Michael E. Baser, Richard T. Ramsden, Valerie Newton, D G R Evans, Andrew J Wallace
Publikováno v:
Journal of Medical Genetics. 37:944-947
Editor—We have previously reported on a large clinical study of patients with neurofibromatosis 2 (NF2)1and described the usefulness of audiological screening in early detection of VS in NF2.2 Although DNA diagnosis is possible by linkage analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fdc8346561fb9b824f68db67d1ee513
https://doi.org/10.1136/jmg.37.12.944
https://doi.org/10.1136/jmg.37.12.944
Autor:
Frances Hickson, Valerie Newton
Publikováno v:
Deafness & Education International. 2:75-85
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a9f08d5a2c8d58126372185aa20c361
https://doi.org/10.1179/146431500790561206
https://doi.org/10.1179/146431500790561206
Autor:
Jiu Mu Zhou, Chuan Yu Liang, Dorothy Trump, Karen P. Steel, James Walsh, Xiao Mei Ke, Sarah Bundey, Xue-Zhong Liu, Steve D.M. Brown, Carolyn Hope, Li Ron Xu, Valerie Newton
Publikováno v:
The American Journal of Human Genetics. 63:909-912
This work was supported by the Medical Research Council (U.K.), Defeating Deafness—the Hearing Research Trust, and SENSE and by European Community grant CT96-1324. C.H. acknowledges support from the British Retinitis Pigmentosa Society and the Birm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3198ddf21b99657ed5650eac52b5b09f
https://doi.org/10.1086/302026
https://doi.org/10.1086/302026