D
Dafydd Stephens
Researcher at University Hospital of Wales
Publications - 80
Citations - 2245
Dafydd Stephens is an academic researcher from University Hospital of Wales. The author has contributed to research in topics: Hearing loss & King–Kopetzky syndrome. The author has an hindex of 26, co-authored 80 publications receiving 2103 citations. Previous affiliations of Dafydd Stephens include Swansea University & University of Wales.
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Journal ArticleDOI
Candidature for and delivery of audiological services: special needs of older people.
Jürgen Kiessling,MK Pichora-Fuller,Stuart Gatehouse,Dafydd Stephens,Stig Arlinger,Theresa H. Chisolm,Adrian Davis,Norman P. Erber,Louise Hickson,Alice E. Holmes,Ulf Rosenhall,H. von Wedel +11 more
TL;DR: Canada, Australia, -Communication Disiibility in Ageing Rcscarch Unit, The IJnivcrsity of Queensland.
Journal ArticleDOI
Impairment, disability and handicap in audiology: towards a consensus.
Dafydd Stephens,Raymond Hétu +1 more
TL;DR: It is argued that the WHO definitions of impairment, disability and handicap have a useful role in understanding the processes of audiological rehabilitation and propose further classifications of the three.
Journal ArticleDOI
Translations of the International Outcome inventory for Hearing Aids (IOI-HA).
TL;DR: Translations of the International Outcome Inventory for Hearing Aids (IOI-HA): Traducciones del Inventario Internacional de Resultados for Auxiliares Auditivos.
Journal ArticleDOI
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations
Kim Cryns,Markus Pfister,Ronald J.E. Pennings,Steven J. H. Bom,Kris Flothmann,Goele Caethoven,Hannie Kremer,Isabelle Schatteman,Karen A Köln,Tímea Tóth,Susan Kupka,Nikolaus Blin,Peter Nürnberg,Holger Thiele,Paul Van de Heyning,William Reardon,Dafydd Stephens,Cor W. R. J. Cremers,Richard J.H. Smith,Guy Van Camp +19 more
TL;DR: In this paper, a mutation screening of the WFS1 gene in eight autosomal dominant families and twelve sporadic cases in which affected persons have low-frequency sensorineural hearing impairment (LFSNHI) was performed.
Journal ArticleDOI
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment
E. Van Eyken,G. Van Camp,Erik Fransen,Vedat Topsakal,J.J. Hendrickx,Kelly Demeester,P. Van de Heyning,Elina Mäki-Torkko,Samuli Hannula,Martti Sorri,Mona Jensen,Agnete Parving,Michael Bille,Manuela Baur,Markus Pfister,Amanda Bonaconsa,Manuela Mazzoli,Eva Orzan,Angeles Espeso,Dafydd Stephens,Katia Verbruggen,Joke Huyghe,Ingeborg Dhooge,Patrick L. M. Huygen,Hannie Kremer,Cor W. R. J. Cremers,Sylvia J. W. Kunst,Minna Manninen,Ilmari Pyykkö,Amalia Diaz Lacava,Michael Steffens,Thomas F. Wienker,L. Van Laer +32 more
TL;DR: This study finds an association between ARHI and GSTT1 and GSTM1 in the Finnish population sample, and with NAT2*6A in the general European population sample; the latter finding replicates previously published data.