Elona Cama
Padova, Italy
Last Updated: 09/26/2026
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Found 10 publications
Isoform-Specific TRIOBP Truncating Variants in Deafness, Autosomal Recessive 28: A Case Study of Postlingual Moderate Sensorineural Hearing Loss.
Journal: The journal of applied laboratory medicine
Published: December 09, 2025
Preservation of Distortion Product Otoacoustic Emissions in OTOF -Related Hearing Impairment.
Journal: Ear and hearing
Published: September 07, 2023
Electrocochleography in Auditory Neuropathy Related to Mutations in the OTOF or OPA1 Gene.
Journal: Audiology research
Published: September 08, 2021
Certolizumab for the treatment of psoriasis and psoriatic arthritis: a real-world multicentre Italian study.
Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: February 26, 2020
Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotype.
Journal: Journal of human genetics
Published: February 17, 2020
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.
Journal: International journal of pediatric otorhinolaryngology
Published: August 01, 2017
Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction.
Journal: Brain : a journal of neurology
Published: March 27, 2016
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation.
Journal: Brain : a journal of neurology
Published: January 08, 2015
Abnormal Cochlear Potentials in Friedreich's Ataxia Point to Disordered Synchrony of Auditory Nerve Fiber Activity.
Journal: Neuro-degenerative diseases
Published: August 05, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026