| The universal newborn hearing screening program at the University Hospital of Ferrara: focus on costs and software solutions A Ciorba, S Hatzopoulos, M Busi, P Guerrini, J Petruccelli, A Martini International journal of pediatric otorhinolaryngology 72 (6), 807-816, 2008 | 41 | 2008 |
| LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations A Sensi, S Ceruti, P Trevisi, F Gualandi, M Busi, I Donati, M Neri, A Ferlini, ... American journal of medical genetics Part A 155 (5), 1096-1101, 2011 | 30 | 2011 |
| Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects V Guaran, L Astolfi, A Castiglione, E Simoni, E Olivetto, M Galasso, ... International journal of molecular medicine 32 (4), 785-794, 2013 | 25 | 2013 |
| Cochlear implant outcomes and genetic mutations in children with ear and brain anomalies M Busi, M Rosignoli, A Castiglione, F Minazzi, P Trevisi, C Aimoni, ... BioMed Research International 2015, 2015 | 23 | 2015 |
| Syndromic hearing loss: an update A Castiglione, M Busi, A Martini Hearing, Balance and Communication 11 (3), 146-159, 2013 | 18 | 2013 |
| Novel mutations in the SLC26A4 gene M Busi, A Castiglione, MT Masieri, A Ravani, V Guaran, L Astolfi, P Trevisi, ... International Journal of Pediatric Otorhinolaryngology 76 (9), 1249-1254, 2012 | 18 | 2012 |
| Association of the 4 g/5 g polymorphism of plasminogen activator inhibitor-1 gene with sudden sensorineural hearing loss. A case control study SH Cho, H Chen, IS Kim, C Yokose, J Kang, D Cho, C Cai, S Palma, ... BMC Ear, Nose and Throat Disorders 12, 1-6, 2012 | 17 | 2012 |
| Hearing threshold assessment in young children with electrocochleograpy (EcochG) and auditory brainstem responses (ABR): Experience at the University Hospital of Ferrara C Aimoni, A Ciorba, R Bovo, P Trevisi, M Busi, A Martini Auris Nasus Larynx 37 (5), 553-557, 2010 | 12 | 2010 |
| Auricular involvement of a multifocal non-AIDS Kaposi's sarcoma: a case report M Busi, E Altieri, A Ciorba, C Aimoni Acta Otorhinolaryngologica Italica 34 (2), 146, 2014 | 9 | 2014 |
| Audiological profiles and gjb2, gjb6 mutations: A retrospective study on genetic and clinical data from 2003 to 2008 A Berto, D Pellati, A Castiglione, M Busi, P Trevisi, F Gualandi, A Ferlini, ... Audiological Medicine 7 (2), 93-105, 2009 | 6 | 2009 |
| Hearing, Balance and Communication A Castiglione, M Busi, A Martini Rev Healthcare 13 (2), 146-59, 2015 | 5 | 2015 |
| Navigating the Usher Syndrome Genetic Landscape: An Evaluation of the Associations between Specific Genes and Quality Categories of Cochlear Implant Outcomes M Busi, A Castiglione Audiology Research 14 (2), 254-263, 2024 | | 2024 |
| Research Article Cochlear Implant Outcomes and Genetic Mutations in Children with Ear and Brain Anomalies M Busi, M Rosignoli, A Castiglione, F Minazzi, P Trevisi, C Aimoni, ... | | 2015 |
| Role of a Plasminogen Activator Inhibitor-1 4G/5G polymorphism in the development and clinical outcome of Idiopathic Sudden Sensorineural Hearing Loss J Kim, H Chen, I Kim, C Yokose, C Cai, S Palma, M Busi, A Martini, TJ Yoo, ... Journal of Allergy and Clinical Immunology 129 (2), AB79, 2012 | | 2012 |
| Ear and brain neuroradiological findings and outcomes in cochlear-implant candidate children M Busi, P Trevisi, E Destro, F Calzolari, A Martini IAPA 2008 The XIV International Symposium in Audiological Medicine 1, 46-46, 2008 | | 2008 |
| Role of the 4G/5G Polymorphism of Plasminogen Activator Inhibitor-1 Gene in Idiopathic Sudden Sensorineural Hearing Loss, A Case Control Study SH Cho, H Chen, IS Kim, C Yokose, J Kang, C Cai, S Palma, M Busi, ... | | |
