All Stories

  1. Telemedicine for hearing-impaired patients in Italy

    Article • Acta Otorhinolaryngologica Italica, October 2024, Pacini Editore

    Pietro Scimemi

  2. The Effects of Noise on Children’s Cognitive Performance: A Systematic Review

    Article • Environment and Behavior, April 2024, SAGE Publications

    Pietro Scimemi

  3. Preservation of Distortion Product Otoacoustic Emissions in OTOF-Related Hearing Impairment

    Article • Ear & Hearing, September 2023, Wolters Kluwer Health

    Pietro Scimemi

  4. Novel Pathogenic Variants in PJVK, the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory Neuropathy Spectrum Disorder

    Article • Genes, January 2022, MDPI AG

    Pietro Scimemi

  5. Electrocochleography in Auditory Neuropathy Related to Mutations in the OTOF or OPA1 Gene

    Article • Audiology Research, November 2021, MDPI AG

    Pietro Scimemi

  6. Cochlear implantation in children with Autism Spectrum Disorder (ASD): Outcomes and implant fitting characteristics

    Article • International Journal of Pediatric Otorhinolaryngology, August 2021, Elsevier

    Pietro Scimemi

  7. Reduction of Kir4.1 channel activity in an oxidative stress‐related aging model

    Article • The FASEB Journal, May 2021, Wiley

    Pietro Scimemi

  8. Cochlear Synaptopathy due to Mutations in otof Gene May Result in Stable Mild Hearing Loss and Severe Impairment of Speech Perception

    Article • Ear & Hearing, April 2021, Wolters Kluwer Health

    Pietro Scimemi

  9. An audiological perspective on ‘‘Two further patients with Warsaw breakage syndrome. Is a mild phenotype possible?”

    Article • Molecular Genetics & Genomic Medicine, June 2020, Wiley

    Pietro Scimemi

  10. Speech Perception Changes in the Acoustically Aided, Nonimplanted Ear after Cochlear Implantation: A Multicenter Study

    Article • Journal of Clinical Medicine, June 2020, MDPI AG

    Pietro Scimemi, Mathieu Hotton, Prof. Piotr Henryk Skarzynski

  11. Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotype

    Article • Journal of Human Genetics, May 2020, Springer Science + Business Media

    Pietro Scimemi

  12. Hearing Dysfunction in a Large Family Affected by Dominant Optic Atrophy (OPA8-Related DOA): A Human Model of Hidden Auditory Neuropathy

    Article • Frontiers in Neuroscience, May 2019, Frontiers

    Pietro Scimemi

  13. 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

    Article • International Journal of Pediatric Otorhinolaryngology, January 2018, Elsevier

    Pietro Scimemi

  14. Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction

    Article • Brain, March 2016, Oxford University Press (OUP)

    Pietro Scimemi

  15. Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations

    Article • Hearing Research, December 2015, Elsevier

    Pietro Scimemi

  16. Abnormal Cochlear Potentials in Friedreich's Ataxia Point to Disordered Synchrony of Auditory Nerve Fiber Activity

    Article • Neurodegenerative Diseases, March 2015, Karger Publishers

    Pietro Scimemi

  17. OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation

    Article • Brain, January 2015, Oxford University Press (OUP)

    Pietro Scimemi

  18. Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca 2+ signaling and high-frequency hearing acquisition

    Article • Proceedings of the National Academy of Sciences, August 2012, Proceedings of the National Academy of Sciences

    Pietro Scimemi

  19. BAAV Mediated GJB2 Gene Transfer Restores Gap Junction Coupling in Cochlear Organotypic Cultures from Deaf Cx26Sox10Cre Mice

    Article • PLOS One, August 2011, PLOS

    Pietro Scimemi

  20. Presynaptic and postsynaptic mechanisms underlying auditory neuropathy in patients with mutations in theOTOForOPA1gene

    Article • Audiological Medicine, March 2011, Taylor & Francis

    Pietro Scimemi

  21. The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice

    Article • Human Molecular Genetics, September 2010, Oxford University Press (OUP)

    Pietro Scimemi

  22. The Novel PMCA2 Pump MutationTommyImpairs Cytosolic Calcium Clearance in Hair Cells and Links to Deafness in Mice

    Article • Journal of Biological Chemistry, September 2010, American Society for Biochemistry & Molecular Biology (ASBMB)

    Pietro Scimemi

  23. Abnormal Cochlear Potentials from Deaf Patients with Mutations in the Otoferlin Gene

    Article • Journal of the Association for Research in Otolaryngology, July 2009, Springer Science + Business Media

    Pietro Scimemi

  24. Audiological and electrocochleography findings in hearing-impaired children with connexin 26 mutations and otoacoustic emissions

    Article • European Archives of Oto-Rhino-Laryngology, August 2007, Springer Science + Business Media

    Pietro Scimemi

  25. Auditory neuropathy in systemic sclerosis: a speech perception and evoked potential study before and after cochlear implantation

    Article • European Archives of Oto-Rhino-Laryngology, June 2006, Springer Science + Business Media

    Pietro Scimemi