CAMA, ELONA

CAMA, ELONA  

Dipartimento di Neuroscienze - DNS  

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Risultati 1 - 18 di 18 (tempo di esecuzione: 0.028 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive nonsyndromic sensorineural hearing loss in a consanguineous Tunisian family 2009 CAMA, ELONASANTARELLI, ROSAMARIAARSLAN, EDOARDO + INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY - -
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, FEDERICABETTELLA, ELISAPOLLI, ROBERTACAMA, ELONASCIMEMI, PIETROSANTARELLI, ROSAMARIAMURGIA, ALESSANDRA INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY - -
A rare case of metastases to the maxillary sinus from sigmoid colon adenocarcinoma 2002 CAMA, ELONA + ORL - -
Abnormal cochlear potentials from deaf patients with mutations in the otoferlin gene 2009 SANTARELLI, ROSAMARIASCIMEMI, PIETROCAMA, ELONAARSLAN, EDOARDO + JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY - -
Abnormal cochlear potentials in Friedreich's ataxia point to disordered synchrony of auditory nerve fiber activity 2015 SANTARELLI, ROSAMARIACAMA, ELONAPEGORARO, ELENASCIMEMI, PIETRO NEURODEGENERATIVE DISEASES - -
Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations 2015 SANTARELLI, ROSAMARIACAMA, ELONASCIMEMI, PIETRO + HEARING RESEARCH - -
Audiological and electrocochleography findings in hearing-impaired children with connexin 26 mutations and otoacoustic emissions 2008 SANTARELLI, ROSAMARIACAMA, ELONASCIMEMI, PIETROARSLAN, EDOARDO + EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY - -
Electrocochleography in Auditory Neuropathy Related to Mutations in the OTOF or OPA1 Gene 2021 Santarelli, RScimemi, PCama, E + AUDIOLOGY RESEARCH - -
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.Cama E.Scimemi P.Santarelli R.Murgia A. + JOURNAL OF HUMAN GENETICS - -
Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohort 2009 CAMA, ELONASANTARELLI, ROSAMARIAARSLAN, EDOARDO + INTERNATIONAL JOURNAL OF AUDIOLOGY - -
Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing loss 2009 CAMA, ELONASANTARELLI, ROSAMARIAARSLAN, EDOARDO + INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY - -
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation. 2015 SANTARELLI, ROSAMARIASCIMEMI, PIETROCAMA, ELONA + BRAIN - -
Pathogenetic role of the deafness-related M34T mutation of Cx26 2006 ARSLAN, EDOARDOCAMA, ELONAMAMMANO, FABIO + HUMAN MOLECULAR GENETICS - -
Presynaptic and postsynaptic mechanisms underlying auditory neuropathy in patients with mutations in the OTOF or OPA1 gene 2011 SANTARELLI, ROSAMARIASCIMEMI, PIETROCAMA, ELONAARSLAN, EDOARDO + AUDIOLOGICAL MEDICINE - -
Primary tumors and tumor-like lesions of the eustachian tube: a systematic review of an emerging entity 2012 CAMA, ELONABOSCOLO RIZZO, PAOLOARSLAN, EDOARDO + EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY - -
Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction 2016 SANTARELLI, ROSAMARIACAMA, ELONASCIMEMI, PIETRO + BRAIN - -
Sudden hearing loss in sarcoidosis: otoneurological study and neuroradiological correlates 2011 CAMA, ELONASANTARELLI, ROSAMARIAARSLAN, EDOARDO + ACTA OTORHINOLARYNGOLOGICA ITALICA - -
Temporal Bone High-Resolution Computed Tomography in Non-Syndromic Unilateral Hearing Loss in Children 2012 CAMA, ELONASADUSHI, ORJONASANTARELLI, ROSAMARIAARSLAN, EDOARDO + ORL - -