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P van de Heyning

Showing results (111-120 of 118) with videos related to

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Archives of Otolaryngology--Head & Neck Surgery|November 1, 2001
Therapeutic electrical stimulation of the hypoglossal nerve in obstructive sleep apneaA R Schwartz, M L Bennett, P L Smith, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Human Molecular Genetics|June 17, 1999
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.
Progress in Brain Research|October 25, 2007
Consensus for tinnitus patient assessment and treatment outcome measurement: Tinnitus Research Initiative meeting, Regensburg, July 2006B Langguth, R Goodey, A Azevedo, et al.
Journal of Medical Genetics|May 22, 2007
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairmentE Van Eyken, G Van Camp, E Fransen, et al.
B-ENT|January 30, 2008
Familial aggregation of tinnitus: a European multicentre studyJ J Hendrickx, J R Huyghe, K Demeester, et al.
Acta Oto-Laryngologica. Supplementum|December 17, 2013
Towards a consensus on a hearing preservation classification systemHenryk Skarzynski, P van de Heyning, S Agrawal, et al.
Cochlear Implants International|June 15, 2013
Standards of practice in the field of hearing implantsP Van de Heyning, O Adunka, S L Arauz, et al.
Pageof 12

Showing results (111-120 of 118) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 118 results.
Archives of Otolaryngology--Head & Neck Surgery|November 1, 2001
Therapeutic electrical stimulation of the hypoglossal nerve in obstructive sleep apneaA R Schwartz, M L Bennett, P L Smith, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Human Molecular Genetics|June 17, 1999
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.
Progress in Brain Research|October 25, 2007
Consensus for tinnitus patient assessment and treatment outcome measurement: Tinnitus Research Initiative meeting, Regensburg, July 2006B Langguth, R Goodey, A Azevedo, et al.
Journal of Medical Genetics|May 22, 2007
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairmentE Van Eyken, G Van Camp, E Fransen, et al.
B-ENT|January 30, 2008
Familial aggregation of tinnitus: a European multicentre studyJ J Hendrickx, J R Huyghe, K Demeester, et al.
Acta Oto-Laryngologica. Supplementum|December 17, 2013
Towards a consensus on a hearing preservation classification systemHenryk Skarzynski, P van de Heyning, S Agrawal, et al.
Cochlear Implants International|June 15, 2013
Standards of practice in the field of hearing implantsP Van de Heyning, O Adunka, S L Arauz, et al.
Pageof 12