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Human Genetics|August 19, 2021
A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosisAllan Thomas Højland, Lisse J M Tavernier, Isabelle Schrauwen, et al.
The Lancet. Infectious Diseases|February 27, 2010
Otitis media and its consequences: beyond the earacheAnne Vergison, Ron Dagan, Adriano Arguedas, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 21, 2007
Association of bone morphogenetic proteins with otosclerosisIsabelle Schrauwen, Melissa Thys, Kathleen Vanderstraeten, et al.
American Journal of Human Genetics|February 24, 2009
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosisIsabelle Schrauwen, Megan Ealy, Matthew J Huentelman, et al.
Human Molecular Genetics|June 26, 2007
The coding polymorphism T263I in TGF-beta1 is associated with otosclerosis in two independent populationsMelissa Thys, Isabelle Schrauwen, Kathleen Vanderstraeten, et al.
Cochlear Implants International|February 21, 2012
Multicentre investigation on electrically evoked compound action potential and stapedius reflex: how do these objective measures relate to implant programming parameters?Thierry Van Den Abbeele, Nathalie Noël-Petroff, Istemihan Akin, et al.
Scientific Reports|December 4, 2020
Vestibular Infant Screening (VIS)-Flanders: results after 1.5 years of vestibular screening in hearing-impaired childrenSarie Martens, Ingeborg Dhooge, Cleo Dhondt, et al.
Pediatrics|June 14, 2022
Three Years of Vestibular Infant Screening in Infants With Sensorineural Hearing LossSarie Martens, Ingeborg Dhooge, Cleo Dhondt, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 3, 2007
The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing lossEls Van Eyken, Lut Van Laer, Erik Fransen, et al.
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