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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 9, 2005
Phenotype determination guides swift genotyping of a DFNA2/KCNQ4 family with a hot spot mutation (W276S)Vedat Topsakal, Ronald J E Pennings, Heleen te Brinke, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|September 19, 2008
Clinical outcome of the simplified surgical technique for BAHA implantationMaarten J F de Wolf, Myrthe K S Hol, Patrick L M Huygen, et al.
The Annals of Otology, Rhinology, and Laryngology|December 24, 2008
Nijmegen results with application of a bone-anchored hearing aid in children: simplified surgical techniqueMaarten J F de Wolf, Myrthe K S Hol, Patrick L M Huygen, et al.
Archives of Otolaryngology--Head & Neck Surgery|December 19, 2012
Analysis of factors predicting the success of the bone conduction device headband trial in patients with single-sided deafnessHubert T Faber, Hanneke Kievit, Maarten J F de Wolf, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|January 25, 2003
Effect of exogenous surfactant on ventilatory and clearance function of the rat's eustachian tubeNiels van Heerbeek, Edith L G M Tonnaer, Koen J A O Ingels, et al.
Journal of the Association for Research in Otolaryngology : JARO|May 24, 2006
A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlationRutger F Plantinga, Arjan P M de Brouwer, Patrick L M Huygen, et al.
Audiology & Neuro-Otology|April 18, 2009
Vestibular impairment in a Dutch DFNA15 family with an L289F mutation in POU4F3F J Wendy van Drunen, Robert J Pauw, Rob W J Collin, et al.
Archives of Otolaryngology--Head & Neck Surgery|March 19, 2008
Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p.L289F) in POU4F3Robert J Pauw, F J Wendy van Drunen, Rob W J Collin, et al.
The Laryngoscope|January 19, 2012
Association between bone mineral density and hearing loss in osteogenesis imperfectaFreya K R Swinnen, Els M R De Leenheer, Stefan Goemaere, et al.
Human Mutation|March 12, 2008
SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BORAmit Kochhar, Dana J Orten, Jessica L Sorensen, et al.
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