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P van de Heyning

Showing results (101-110 of 118) with videos related to

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Acta Chirurgica Belgica|July 1, 1996
Surgical treatment of benign tumours of the salivary glandsR Van Hee, M Misset, D Ysebaert, et al.
Cochlear Implants International|September 16, 2008
Open-set speech perception in adult cochlear implant users with ossified cochleaeG Bredberg, B Lindström, W D Baumgartner, et al.
Annals of Human Genetics|February 12, 2009
Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patientsM Thys, I Schrauwen, K Vanderstraeten, et al.
Human Genetics|September 12, 2000
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairmentK Verhoeven, T Fagerheim, S Prasad, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 1, 2016
Safety and effectiveness of the Bonebridge transcutaneous active direct-drive bone-conduction hearing implant at 1-year device useSébastien Schmerber, O Deguine, M Marx, et al.
American Journal of Human Genetics|February 15, 2001
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36K Van Den Bogaert, P J Govaerts, I Schatteman, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochleaL Van Laer, G Van Camp, D van Zuijlen, et al.
Mitochondrion|June 8, 2011
Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European populationS Bonneux, E Fransen, E Van Eyken, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) geneK Verhoeven, R J Ensink, V Tiranti, et al.
Nature Genetics|October 15, 1998
Nonsyndromic hearing impairment is associated with a mutation in DFNA5L Van Laer, E H Huizing, M Verstreken, et al.
Pageof 12

Showing results (101-110 of 118) with videos related to

Sort By:
Pageof 12
Acta Chirurgica Belgica|July 1, 1996
Surgical treatment of benign tumours of the salivary glandsR Van Hee, M Misset, D Ysebaert, et al.
Cochlear Implants International|September 16, 2008
Open-set speech perception in adult cochlear implant users with ossified cochleaeG Bredberg, B Lindström, W D Baumgartner, et al.
Annals of Human Genetics|February 12, 2009
Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patientsM Thys, I Schrauwen, K Vanderstraeten, et al.
Human Genetics|September 12, 2000
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairmentK Verhoeven, T Fagerheim, S Prasad, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 1, 2016
Safety and effectiveness of the Bonebridge transcutaneous active direct-drive bone-conduction hearing implant at 1-year device useSébastien Schmerber, O Deguine, M Marx, et al.
American Journal of Human Genetics|February 15, 2001
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36K Van Den Bogaert, P J Govaerts, I Schatteman, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochleaL Van Laer, G Van Camp, D van Zuijlen, et al.
Mitochondrion|June 8, 2011
Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European populationS Bonneux, E Fransen, E Van Eyken, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) geneK Verhoeven, R J Ensink, V Tiranti, et al.
Nature Genetics|October 15, 1998
Nonsyndromic hearing impairment is associated with a mutation in DFNA5L Van Laer, E H Huizing, M Verstreken, et al.
Pageof 12