Micol Busi

The universal newborn hearing screening program at the University Hospital of Ferrara: Focus on costs and software solutions

Andrea Ciorba, Stavros Hatzopoulos, Micol Busi et al. · International Journal of Pediatric Otorhinolaryngology · 2008 · 34 citations

Health Professions, Audiology, Pediatrics +15

LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations

Alberto Sensi, Stefano Ceruti, Patrizia Trevisi et al. · American Journal of Medical Genetics Part A · 2011 · 31 citations

Medicine, Genetics, Otolaryngology +17

Cochlear Implant Outcomes and Genetic Mutations in Children with Ear and Brain Anomalies

Micol Busi, M. Rosignoli, Alessandro Castiglione et al. · BioMed Research International · 2015 · 25 citations · Full text

Medicine, Audiology, Otolaryngology +17

Association between idiopathic hearing loss and mitochondrial DNA mutations: A study on 169 hearing-impaired subjects

Valeria Guaran, Laura Astolfi, Alessandro Castiglione et al. · International Journal of Molecular Medicine · 2013 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Association of the 4 g/5 g polymorphism of plasminogen activator inhibitor-1 gene with sudden sensorineural hearing loss. A case control study

Seong Cho, Haimei Chen, Il Soo Kim et al. · BMC Ear Nose and Throat Disorders · 2012 · 19 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16