CAMA, ELONA
CAMA, ELONA
Dipartimento di Neuroscienze - DNS
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive nonsyndromic sensorineural hearing loss in a consanguineous Tunisian family
2009 Alemanno, Ms; Cama, Elona; Santarelli, Rosamaria; Carella, M; Zelante, L; Toffolatti, L; Palladino, T; Melchionda, S; Arslan, Edoardo
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
A rare case of metastases to the maxillary sinus from sigmoid colon adenocarcinoma
2002 Cama, Elona; Stefania, Agostino; Riccardo, Ricci; Emanuele, Scarano
Abnormal cochlear potentials from deaf patients with mutations in the otoferlin gene
2009 Santarelli, Rosamaria; DEL CASTILLO, I; RODRIGUEZ BALLESTEROS, M; Scimemi, Pietro; Cama, Elona; Arslan, Edoardo; Starr, A.
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
Audiological and electrocochleography findings in hearing-impaired children with connexin 26 mutations and otoacoustic emissions
2008 Santarelli, Rosamaria; Cama, Elona; Scimemi, Pietro; DAL MONTE, E; Genovese, E; Arslan, Edoardo
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
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.
Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohort
2009 Cama, Elona; Melchionda, S; Palladino, T; Carella, M; Santarelli, Rosamaria; Genovese, E; Benettazzo, F; Zelante, L; Arslan, Edoardo
Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing loss
2009 Cama, Elona; Alemanno, Ms; Bellacchio, E; Santarelli, Rosamaria; Carella, M; Zelante, L; Palladino, T; Inches, I; DI PAOLA, F; Arslan, Edoardo; Melchionda, S.
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.
Pathogenetic role of the deafness-related M34T mutation of Cx26
2006 Bicego, M; Beltramello, M; Carella, M; Piazza, V; Zelante, L; Bukauskas, Ff; Arslan, Edoardo; Cama, Elona; Pantano, S; Bruzzone, R; D'Andrea, P; D'Andrea, P; Mammano, Fabio
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
Presynaptic and postsynaptic mechanisms underlying auditory neuropathy in patients with mutations in the OTOF or OPA1 gene
2011 Santarelli, Rosamaria; Starr, Arnold; Del Castillo, Ignacio; Huang, Taosheng; Scimemi, Pietro; Cama, Elona; Rossi, Roberta; Arslan, Edoardo
Primary tumors and tumor-like lesions of the eustachian tube: a systematic review of an emerging entity
2012 Enrico, Muzzi; Cama, Elona; BOSCOLO RIZZO, Paolo; Franco, Trabalzini; Arslan, Edoardo
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
Sudden hearing loss in sarcoidosis: otoneurological study and neuroradiological correlates
2011 Cama, Elona; Santarelli, Rosamaria; Enrico, Muzzi; Ingrid, Inches; Stefano, Curtolo; FRANCESCO DI, Paola; Arslan, Edoardo; Enzo, Faccini
Temporal Bone High-Resolution Computed Tomography in Non-Syndromic Unilateral Hearing Loss in Children
2012 Cama, Elona; Ingrid, Inches; Enrico, Muzzi; Sadushi, Orjona; Santarelli, Rosamaria; Wladimiro De, Colle; Roberta, Rossi; Francesco di, Paola; Arslan, Edoardo