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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|January 19, 2021
Auditory processing disorder in children: the value of a multidisciplinary assessmentIsabelle Rouillon, Aude de Lamaze, Marlène Ribot, et al.International Journal of Pediatric Otorhinolaryngology|February 6, 2023
Analysis of specific risk factors of neurodevelopmental disorder in hearing-impaired infants under ten months of age: "EnTNDre" an opening research stemming from a transdisciplinary partnershipSalomé Akrich, Erika Parlato de Oliveira, Claire Favrot-Meunier, et al.Biochemical and Biophysical Research Communications|March 17, 2010
Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever!Sandrine Marlin, Delphine Feldmann, Yann Nguyen, et al.Journal of Clinical Microbiology|September 28, 2007
Evaluation of cytomegalovirus (CMV) DNA quantification in dried blood spots: retrospective study of CMV congenital infectionChristelle Vauloup-Fellous, Aurélie Ducroux, Vincent Couloigner, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 10, 2023
Recurrent Benign Paroxysmal Positional Vertigo in DFNB16 Patients with Biallelic STRC Gene DeletionsSophie Achard, Margaux Campion, Marine Parodi, et al.Clinical Genetics|June 28, 2024
HDR syndrome: Large cohort and systematic reviewNicolas Rive Le Gouard, Valentin Lafond-Rive, Laurence Jonard, et al.Biomedicines|August 28, 2025
Vestibular Deficit in Patients with Waardenburg SyndromeMathilde Benifla, Margaux Serey-Gaut, Emilie Bois, et al.The Journal of Pediatrics|October 25, 2025
Hearing Trajectories in Congenital Cytomegalovirus Infection: A 4-Year Follow-Up StudyHugo Delille, Marine Parodi, Jean-François Magny, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 16, 2013
Discovery of a large deletion of KAL1 in 2 deaf brothersSandrine Marlin, Sandra Chantot-Bastaraud, Albert David, et al.Human Mutation|February 26, 2017
EDNRB mutations cause Waardenburg syndrome type II in the heterozygous stateSarah Issa, Nadege Bondurand, Emmanuelle Faubert, et al.Pageof 7