Rosamaria Santarelli

Publication Activity (10 Years)

Years Active: 2020-2022
Publications (10 Years): 3

Top Topics

Spectrum Disorder

Computed Tomography

Top Venues

Molecular genetics & genomic medicine

Audiology research

This page only lists publications with an associated author ORCID identifier.

Publications

María Domínguez-Ruiz, Montserrat Rodríguez-Ballesteros, Marta Gandía, Elena Gómez-Rosas, Manuela Villamar, Pietro Scimemi, Patrizia Mancini, Nanna D Rendtorff, Miguel Angel Moreno-Pelayo, Lisbeth Tranebjaerg, Carme Medà, Rosamaria Santarelli, Ignacio Del Castillo
Novel Pathogenic Variants in PJVK , the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory Neuropathy Spectrum Disorder. Genes 13 (1) (2022)
Rosamaria Santarelli, Pietro Scimemi, Chiara La Morgia, Elona Cama, Ignacio Del Castillo, Valerio Carelli
Electrocochleography in Auditory Neuropathy Related to Mutations in the OTOF or OPA1 Gene. Audiology research 11 (4) (2021)
Davide Brotto, Renzo Manara, Pietro Scimemi, Sorrentino Flavia, Silvia Montino, Francesca Maritan, Ezio Caserta, Elisa Lovo, Alessandro Martini, Rosamaria Santarelli, Patrizia Trevisi
An audiological perspective on ''Two further patients with Warsaw breakage syndrome. Is a mild phenotype possible?" Molecular genetics & genomic medicine 8 (9) (2020)