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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 20, 2011
Otitis media with effusion: an underestimated cause of hearing loss in infantsAn Boudewyns, Frank Declau, Jenneke Van den Ende, et al.Frontiers in Psychology|October 5, 2020
Bimodal Therapy for Chronic Subjective Tinnitus: A Randomized Controlled Trial of EMDR and TRT Versus CBT and TRTTine Roanna Luyten, Laure Jacquemin, Nancy Van Looveren, et al.American Journal of Human Genetics|August 16, 2006
A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 geneGuy Van Camp, Rikkert L Snoeckx, Nele Hilgert, et al.American Journal of Human Genetics|March 12, 2004
Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4)Francesca Donaudy, Rik Snoeckx, Markus Pfister, 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.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.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.Pageof 3