Annamaria Franze - Publications

Vascular Factors in Patients with Midlife Sensorineural Hearing Loss and the Progression to Mild Cognitive Impairment.

Journal: Medicina (Kaunas, Lithuania)

Published: January 20, 2023

The Absence of Permanent Sensorineural Hearing Loss in a Cohort of Children with SARS-CoV-2 Infection and the Importance of Performing the Audiological "Work-Up".

Journal: Children (Basel, Switzerland)

Published: August 31, 2022

NeonaTal Assisted TelerehAbilitation (T.A.T.A. Web App) for Hearing-Impaired Children: A Family-Centered Care Model for Early Intervention in Congenital Hearing Loss.

Journal: Audiology research

Published: March 02, 2022

Integrated Bimodal Fitting for Unilateral CI Users with Residual Contralateral Hearing.

Journal: Audiology research

Published: April 08, 2021

Targeted Audiological Surveillance Program in Campania, Italy.

Journal: Indian pediatrics

Published: January 07, 2021

Performance and characteristics of the Newborn Hearing Screening Program in Campania region (Italy) between 2013 and 2019.

Journal: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery

Published: January 07, 2021

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

Intragenic Deletion in MACROD2: A Family with Complex Phenotypes Including Microcephaly, Intellectual Disability, Polydactyly, Renal and Pancreatic Malformations.

Journal: Cytogenetic and genome research

Published: December 18, 2018

Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss.

Journal: European journal of human genetics : EJHG

Published: November 22, 2017

Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection.

Journal: European journal of human genetics : EJHG

Published: July 12, 2017

X-Linked Sensorineural Hearing Loss: A Literature Review.

Journal: Current genomics

Published: April 20, 2017

Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic sequence variants.

Journal: BMC medical genetics

Published: September 02, 2016