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Audiology Research|March 25, 2024
Navigating the Usher Syndrome Genetic Landscape: An Evaluation of the Associations between Specific Genes and Quality Categories of Cochlear Implant OutcomesMicol Busi, Alessandro CastiglioneInternational Journal of Pediatric Otorhinolaryngology|April 9, 2008
The universal newborn hearing screening program at the University Hospital of Ferrara: focus on costs and software solutionsAndrea Ciorba, Stavros Hatzopoulos, Micol Busi, et al.American Journal of Medical Genetics. Part A|April 12, 2011
LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutationsAlberto Sensi, Stefano Ceruti, Patrizia Trevisi, et al.Biomed Research International|August 4, 2015
Cochlear Implant Outcomes and Genetic Mutations in Children with Ear and Brain AnomaliesMicol Busi, Monica Rosignoli, Alessandro Castiglione, et al.International Journal of Pediatric Otorhinolaryngology|June 22, 2012
Novel mutations in the SLC26A4 geneMicol Busi, Alessandro Castiglione, Marina Taddei Masieri, et al.International Journal of Molecular Medicine|August 24, 2013
Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjectsValeria Guaran, Laura Astolfi, Alessandro Castiglione, et al.BMC Ear, Nose, and Throat Disorders|June 8, 2012
Association of the 4 g/5 g polymorphism of plasminogen activator inhibitor-1 gene with sudden sensorineural hearing loss. A case control studySeong Ho Cho, Haimei Chen, Il Soo Kim, et al.Journal of Otolaryngology - Head & Neck Surgery = Le Journal D'Oto-Rhino-Laryngologie Et De Chirurgie Cervico-Faciale|July 21, 2025
Diagnostic Yield and Genetic Variation in 85 Swedish Patients with Mild to Profound Hearing Loss Analyzed by Whole Genome SequencingJohanna Elander, Tove Ullmark, Karolina Löwgren, et al.Pageof 1