Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

I Schatteman

Showing results (1-10 of 17) with videos related to

Pageof 2
Sort By:
Acta Oto-Rhino-Laryngologica Belgica|November 2, 2004
Allograft tympanoplastyT Somers, I Schatteman, F E Offeciers
Acta Oto-Rhino-Laryngologica Belgica|July 3, 2003
Results of 100 vestibular schwannoma operationsTh Somers, F E Offeciers, I Schatteman
Acta Oto-Laryngologica. Supplementum|January 1, 1997
Selective vestibular neurectomy in Menière's disease: a reviewP H Van de Heyning, J Verlooy, I Schatteman, et al.
Advances in Oto-Rhino-Laryngology|January 25, 2007
Transient depression of inner ear function after stapedotomy: skeeter versus CO(2) laser techniqueT Somers, J P Vercruysse, A Zarowski, et al.
The American Journal of Otology|November 27, 1998
A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing lossP J Govaerts, G De Ceulaer, K Daemers, et al.
Journal of Medical Genetics|March 21, 1998
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)N J Lench, A F Markham, R F Mueller, et al.
Genes and Immunity|February 26, 2010
Involvement of T-cell receptor-beta alterations in the development of otosclerosis linked to OTSC2I Schrauwen, K Venken, 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.
The American Journal of Otology|September 19, 2000
Audiometric analysis of a Belgian family linked to the DFNA10 locusM Verstreken, F Declau, I Schatteman, 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.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Acta Oto-Rhino-Laryngologica Belgica|November 2, 2004
Allograft tympanoplastyT Somers, I Schatteman, F E Offeciers
Acta Oto-Rhino-Laryngologica Belgica|July 3, 2003
Results of 100 vestibular schwannoma operationsTh Somers, F E Offeciers, I Schatteman
Acta Oto-Laryngologica. Supplementum|January 1, 1997
Selective vestibular neurectomy in Menière's disease: a reviewP H Van de Heyning, J Verlooy, I Schatteman, et al.
Advances in Oto-Rhino-Laryngology|January 25, 2007
Transient depression of inner ear function after stapedotomy: skeeter versus CO(2) laser techniqueT Somers, J P Vercruysse, A Zarowski, et al.
The American Journal of Otology|November 27, 1998
A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing lossP J Govaerts, G De Ceulaer, K Daemers, et al.
Journal of Medical Genetics|March 21, 1998
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)N J Lench, A F Markham, R F Mueller, et al.
Genes and Immunity|February 26, 2010
Involvement of T-cell receptor-beta alterations in the development of otosclerosis linked to OTSC2I Schrauwen, K Venken, 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.
The American Journal of Otology|September 19, 2000
Audiometric analysis of a Belgian family linked to the DFNA10 locusM Verstreken, F Declau, I Schatteman, 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.
Pageof 2