Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Pietro Scimemi

Showing results (11-20 of 19) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 19 results.
International Journal of Pediatric Otorhinolaryngology|August 13, 2021
Cochlear implantation in children with Autism Spectrum Disorder (ASD): Outcomes and implant fitting characteristicsPatrizia Mancini, Laura Mariani, Maria Nicastri, et al.
Plos One|August 31, 2011
BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre miceGiulia Crispino, Giovanni Di Pasquale, Pietro Scimemi, et al.
Brain : a Journal of Neurology|January 8, 2015
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantationRosamaria Santarelli, Roberta Rossi, Pietro Scimemi, et al.
The Journal of Biological Chemistry|September 10, 2010
The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in miceMario Bortolozzi, Marisa Brini, Nick Parkinson, et al.
Human Molecular Genetics|September 23, 2010
The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in miceMelanie Schütz, Pietro Scimemi, Paromita Majumder, et al.
Journal of Human Genetics|May 30, 2020
Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotypeFederica Cesca, Elisa Bettella, Roberta Polli, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2012
Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisitionLaura Rodriguez, Elena Simeonato, Pietro Scimemi, et al.
Genes|January 21, 2022
Novel Pathogenic Variants in <i>PJVK</i>, the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory Neuropathy Spectrum DisorderMaría Domínguez-Ruiz, Montserrat Rodríguez-Ballesteros, Marta Gandía, et al.
Journal of Clinical Medicine|June 11, 2020
Speech Perception Changes in the Acoustically Aided, Nonimplanted Ear after Cochlear Implantation: A Multicenter StudyMario A Svirsky, Arlene C Neuman, Jonathan D Neukam, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
International Journal of Pediatric Otorhinolaryngology|August 13, 2021
Cochlear implantation in children with Autism Spectrum Disorder (ASD): Outcomes and implant fitting characteristicsPatrizia Mancini, Laura Mariani, Maria Nicastri, et al.
Plos One|August 31, 2011
BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre miceGiulia Crispino, Giovanni Di Pasquale, Pietro Scimemi, et al.
Brain : a Journal of Neurology|January 8, 2015
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantationRosamaria Santarelli, Roberta Rossi, Pietro Scimemi, et al.
The Journal of Biological Chemistry|September 10, 2010
The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in miceMario Bortolozzi, Marisa Brini, Nick Parkinson, et al.
Human Molecular Genetics|September 23, 2010
The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in miceMelanie Schütz, Pietro Scimemi, Paromita Majumder, et al.
Journal of Human Genetics|May 30, 2020
Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotypeFederica Cesca, Elisa Bettella, Roberta Polli, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2012
Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisitionLaura Rodriguez, Elena Simeonato, Pietro Scimemi, et al.
Genes|January 21, 2022
Novel Pathogenic Variants in <i>PJVK</i>, the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory Neuropathy Spectrum DisorderMaría Domínguez-Ruiz, Montserrat Rodríguez-Ballesteros, Marta Gandía, et al.
Journal of Clinical Medicine|June 11, 2020
Speech Perception Changes in the Acoustically Aided, Nonimplanted Ear after Cochlear Implantation: A Multicenter StudyMario A Svirsky, Arlene C Neuman, Jonathan D Neukam, et al.
Pageof 2