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Pietro SCIMEMI
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引用次数
引用次数
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Cochlear implant–state of the art
T Lenarz
Laryngo-rhino-otologie 96 (S 01), S123-S151, 2017
3542017
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation
R Santarelli, R Rossi, P Scimemi, E Cama, ML Valentino, C La Morgia, ...
Brain 138 (3), 563-576, 2015
1022015
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
M Schuetz, P Scimemi, P Majumder, RD De Siati, G Crispino, L Rodriguez, ...
Human molecular genetics 19 (24), 4759-4773, 2010
792010
BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice
G Crispino, G Di Pasquale, P Scimemi, L Rodriguez, F Galindo Ramirez, ...
PloS one 6 (8), e23279, 2011
782011
Abnormal cochlear potentials from deaf patients with mutations in the otoferlin gene
R Santarelli, I Del Castillo, M Rodríguez-Ballesteros, P Scimemi, E Cama, ...
Journal of the Association for Research in Otolaryngology 10, 545-556, 2009
742009
The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in mice
M Bortolozzi, M Brini, N Parkinson, G Crispino, P Scimemi, RD De Siati, ...
Journal of Biological Chemistry 285 (48), 37693-37703, 2010
692010
Cochlear microphonic potential recorded by transtympanic electrocochleography in normally-hearing and hearing-impaired ears
R Santarelli, P Scimemi, E Dal Monte, E Arslan
Acta otorhinolaryngologica italica 26 (2), 78, 2006
692006
Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations
R Santarelli, I del Castillo, E Cama, P Scimemi, A Starr
Hearing research 330, 200-212, 2015
582015
Reduced phosphatidylinositol 4, 5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisition
L Rodriguez, E Simeonato, P Scimemi, F Anselmi, B Calì, G Crispino, ...
Proceedings of the National Academy of Sciences 109 (35), 14013-14018, 2012
512012
Auditory brainstem responses to clicks and tone bursts in C57 BL/6J mice
P Scimemi, R Santarelli, A Selmo, F Mammano
Acta Otorhinolaryngologica Italica 34 (4), 264, 2014
442014
Audiological and electrocochleography findings in hearing-impaired children with connexin 26 mutations and otoacoustic emissions
R Santarelli, E Cama, P Scimemi, E Dal Monte, E Genovese, E Arslan
European archives of oto-rhino-laryngology 265, 43-51, 2008
392008
Auditory neuropathy in systemic sclerosis: a speech perception and evoked potential study before and after cochlear implantation
R Santarelli, P Scimemi, E Dal Monte, E Genovese, E Arslan
European Archives of Oto-Rhino-Laryngology and Head & Neck 263, 809-815, 2006
362006
Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction
PJ Kullar, J Quail, P Lindsey, JA Wilson, R Horvath, P Yu-Wai-Man, ...
Brain 139 (6), e33-e33, 2016
212016
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
F Cesca, E Bettella, R Polli, E Cama, P Scimemi, R Santarelli, A Murgia
International Journal of Pediatric Otorhinolaryngology 104, 88-93, 2018
162018
Presynaptic and postsynaptic mechanisms underlying auditory neuropathy in patients with mutations in the OTOF or OPA1 gene
R Santarelli, A Starr, I Del Castillo, T Huang, P Scimemi, E Cama, R Rossi, ...
Audiological Medicine 9 (2), 59-66, 2011
142011
Novel Pathogenic Variants in PJVK, the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory …
M Domínguez-Ruiz, M Rodríguez-Ballesteros, M Gandía, E Gómez-Rosas, ...
Genes 13 (1), 149, 2022
102022
Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotype
F Cesca, E Bettella, R Polli, E Leonardi, MC Aspromonte, B Sicilian, ...
Journal of Human Genetics 65 (10), 855-864, 2020
92020
Cochlear implantation in children with Autism Spectrum Disorder (ASD): Outcomes and implant fitting characteristics
P Mancini, L Mariani, M Nicastri, S Cavicchiolo, I Giallini, P Scimemi, ...
International Journal of Pediatric Otorhinolaryngology 149, 110876, 2021
82021
Abnormal cochlear potentials in Friedreich's ataxia point to disordered synchrony of auditory nerve fiber activity
R Santarelli, E Cama, E Pegoraro, P Scimemi
Neurodegenerative Diseases 15 (2), 114-120, 2015
82015
Cochlear synaptopathy due to mutations in OTOF gene may result in stable mild hearing loss and severe impairment of speech perception
R Santarelli, P Scimemi, M Costantini, M Domínguez-Ruiz, ...
Ear and Hearing 42 (6), 1627-1639, 2021
72021
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