SCIMEMI, PIETRO
SCIMEMI, PIETRO
Dipartimento di Neuroscienze - DNS
Influence of Noise Level and Reverberation on Children’s Performance and Effort in Primary Schools
2025 Pittana, I.; Pavarin, C.; Pavanello, I.; Di Bella, A.; Romagnoni, P.; Scimemi, P.; Cappelletti, F.
Telemedicine for hearing-impaired patients in Italy
2024 Ghiselli, Sara; Sorrentino, Flavia; Lazzerini, Francesco; Rabito, Chiara; Murri, Alessandra; Scimemi, Pietro
The Effects of Noise on Children’s Cognitive Performance: A Systematic Review
2024 Gheller, F.; Spicciarelli, G.; Scimemi, P.; Arfé, B.
MRI AND FUNCTIONAL STUDY OF THE EIGHT CRANIAL NERVE IN CANVAS PATIENTS
2023 Tierro, B; Salvalaggio, A; Manara, R; Bonora, C; Gallo, C; Scimemi, P; Valeggia, S; Cacciavillani, M; Currò, R; Castellani, F; Pegoraro, E; Bello, L; Ferrarini, M; Fabrizi, G; Cortese, A; Santarelli, R; Briani, C
Preservation of Distortion Product Otoacoustic Emissions in OTOF-Related Hearing Impairment
2023 Santarelli, Rosamaria; Scimemi, Pietro; Cama, Elona; Domínguez-Ruiz, María; Bonora, Chiara; Gallo, Chiara; Rodríguez-Ballesteros, Montserrat; del Castillo, Ignacio
Ricordo del prof. Edoardo Arslan
2023 Scimemi, Pietro
Novel Pathogenic Variants in PJVK, the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory Neuropathy Spectrum Disorder
2022 Dominguez-Ruiz, M.; Rodriguez-Ballesteros, M.; Gandia, M.; Gomez-Rosas, E.; Villamar, M.; Scimemi, P.; Mancini, P.; Rendtorff, N. D.; Moreno-Pelayo, M. A.; Tranebjaerg, L.; Meda, C.; Santarelli, R.; Del Castillo, I.
Cochlear implantation in children with Autism Spectrum Disorder (ASD): outcomes and implant fitting characteristics
2021 Mancini, Patrizia; Mariani, Laura; Nicastri, Maria; Cavicchiolo, Sara; Giallini, Ilaria; Scimemi, Pietro; Zanetti, Diego; Montino, Silvia; Lovo, Elisa; Di Berardino, Federica; Trevisi, Patrizia; Santarelli, Rosamaria
Cochlear synaptopathy due to mutations in OTOF gene may result in stable mild hearing loss and severe impairment of speech perception
2021 Santarelli, Rosamaria; Scimemi, Pietro; Costantini, Marco; Domìnguez-Ruiz, Maria; Rodrìguez-Ballesteros, Montserrat; del Castillo, Ignacio
Electrocochleography in Auditory Neuropathy Related to Mutations in the OTOF or OPA1 Gene
2021 Santarelli, R; Scimemi, P; La Morgia, C; Cama, E; del Castillo, I; Carelli, V
Reduction of Kir4.1 channel activity in an oxidative stress‐related aging model
2021 Remigante, Alessia; Morabito, Rossana; Marino, Angela; Scimemi, Pietro; Picco, Cristiana; Santarelli, Rosamaria; Zifarelli, Giovanni; Dossena, Silvia; Pusch, Michael
An audiological perspective on ‘‘Two further patients with Warsaw breakage syndrome. Is a mild phenotype possible?”
2020 Brotto, D.; Manara, R.; Scimemi, P.; Sorrentino, F.; Montino, S.; Maritan, F.; Caserta, E.; Lovo, E.; Martini, A.; Santarelli, R.; Trevisi, P.
Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotype
2020 Cesca, F.; Bettella, E.; Polli, R.; Leonardi, E.; Aspromonte, M. C.; Sicilian, B.; Stanzial, F.; Benedicenti, F.; Sensi, A.; Ciorba, A.; Bigoni, S.; Cama, E.; Scimemi, P.; Santarelli, R.; Murgia, A.
Speech Perception Changes in the Acoustically Aided, Nonimplanted Ear after Cochlear Implantation: A Multicenter Study
2020 Svirsky, Mario A; Neuman, Arlene C; Neukam, Jonathan D; Lavender, Annette; Miller, Margaret K; Aaron, Ksenia A; Skarzynski, Piotr H; Cywka, Katarzyna B; Skarzynski, Henryk; Truy, Eric; Seldran, Fabien; Hermann, Ruben; Govaerts, Paul; De Ceulaer, Geert; Bergeron, Francois; Hotton, Matthieu; Moran, Michelle; Dowell, Richard C; Goffi-Gomez, Maria Valeria Schmidt; Magalhães, Ana Tereza de Matos; Santarelli, Rosamaria; Scimemi, Pietro
Hearing Dysfunction in a Large Family Affected by Dominant Optic Atrophy (OPA8-Related DOA): A Human Model of Hidden Auditory Neuropathy
2019 Santarelli, Rosamaria; La Morgia, Chiara; Valentino, Maria Lucia; Barboni, Piero; Monteleone, Anna; Scimemi, Pietro; Carelli, Valerio
A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family members
2018 Cesca, Federica; Bettella, Elisa; Polli, Roberta; Cama, Elona; Scimemi, Pietro; Santarelli, Rosamaria; Murgia, Alessandra
Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction
2016 Santarelli, Rosamaria; Cama, Elona; Scimemi, Pietro; La Morgia, Chiara; Caporali, Leonardo; Valentino, Maria Lucia; Liguori, Rocco; Carelli, Valerio
Abnormal cochlear potentials in Friedreich's ataxia point to disordered synchrony of auditory nerve fiber activity
2015 Santarelli, Rosamaria; Cama, Elona; Pegoraro, Elena; Scimemi, Pietro
Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations
2015 Santarelli, Rosamaria; del Castillo, Ignacio; Cama, Elona; Scimemi, Pietro; Starr, Arnold
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation.
2015 Santarelli, Rosamaria; Rossi, R; Scimemi, Pietro; Cama, Elona; Valentino, Ml; La Morgia, C; Caporali, L; Liguori, R; Magnavita, V; Monteleone, A; Biscaro, A; Arslan, E; Carelli, V.