M. Busi

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

J. Petruccelli, A. Martini, S. Hatzopoulos, 2008, International journal of pediatric otorhinolaryngology.

Novel mutations in the SLC26A4 gene.

A. Ferlini, A. Castiglione, P. Trevisi, 2012, International journal of pediatric otorhinolaryngology.

Auricular involvement of a multifocal non-AIDS Kaposi's sarcoma: a case report

A. Ciorba, C. Aimoni, M. Busi, 2014, Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale.

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

Joseph Kang, Haimei Chen, A. Martini, 2012, BMC Ear, Nose and Throat Disorders.

Role of the 4 G / 5 G Polymorphism of Plasminogen Activator Inhibitor-1 Gene in Idiopathic Sudden Sensorineural Hearing Loss , A Case Control Study

Joseph Kang, Haimei Chen, A. Martini, 2011 .

Syndromic hearing loss: An update

A. Castiglione, A. Martini, M. Busi, 2013 .

Audiological profiles and gjb2, gjb6 mutations: A retrospective study on genetic and clinical data from 2003 to 2008

A. Ferlini, A. Castiglione, P. Trevisi, 2009 .

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

F. Calzolari, E. Granieri, A. Castiglione, 2015, BioMed research international.

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

A. Ferlini, M. Neri, P. Trevisi, 2011, American journal of medical genetics. Part A.

Hearing threshold assessment in young children with electrocochleography (EcochG) and auditory brainstem responses (ABR): experience at the University Hospital of Ferrara.

A Martini, A Ciorba, P. Trevisi, 2010, Auris, nasus, larynx.

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

S. Volinia, M. Galasso, A. Castiglione, 2013, International journal of molecular medicine.