Virginia Corvino
Naples, Italy
Last Updated: 09/26/2026
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Found 8 publications
Bimodal strategy for excellent audiological rehabilitation in a subject with a novel nonsense mutation of the SLC26A4 gene: A case report.
Journal: International journal of pediatric otorhinolaryngology
Published: July 30, 2019
X-Linked Sensorineural Hearing Loss: A Literature Review.
Journal: Current genomics
Published: April 20, 2017
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss.
Journal: Clinical chemistry and laboratory medicine
Published: December 09, 2015
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss.
Journal: Molecular cytogenetics
Published: September 29, 2014
Abnormal thalamic function in patients with vestibular migraine.
Journal: Neurology
Published: May 13, 2014
Exclusion of TNFRSF11B as Candidate Gene for Otosclerosis in Campania Population.
Journal: Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India
Published: July 23, 2013
The rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian population.
Journal: Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale
Published: April 23, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026