Resultats de la cerca - Scimemi, Pietro

Electrocochleography in Auditory Neuropathy Related to Mutations in the OTOF or OPA1 Gene per Santarelli, Rosamaria, Scimemi, Pietro, La Morgia, Chiara, Cama, Elona, del Castillo, Ignacio, Carelli, Valerio

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Abnormal Cochlear Potentials from Deaf Patients with Mutations in the Otoferlin Gene per Santarelli, Rosamaria, del Castillo, Ignacio, Rodríguez-Ballesteros, Montserrat, Scimemi, Pietro, Cama, Elona, Arslan, Edoardo, Starr, Arnold

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Hearing Dysfunction in a Large Family Affected by Dominant Optic Atrophy (OPA8-Related DOA): A Human Model of Hidden Auditory Neuropathy per Santarelli, Rosamaria, La Morgia, Chiara, Valentino, Maria Lucia, Barboni, Piero, Monteleone, Anna, Scimemi, Pietro, Carelli, Valerio

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An audiological perspective on ‘‘Two further patients with Warsaw breakage syndrome. Is a mild phenotype possible?” per Brotto, Davide, Manara, Renzo, Scimemi, Pietro, Sorrentino, Flavia, Montino, Silvia, Maritan, Francesca, Caserta, Ezio, Lovo, Elisa, Martini, Alessandro, Santarelli, Rosamaria, Trevisi, Patrizia

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BAAV Mediated GJB2 Gene Transfer Restores Gap Junction Coupling in Cochlear Organotypic Cultures from Deaf Cx26Sox10Cre Mice per Crispino, Giulia, Di Pasquale, Giovanni, Scimemi, Pietro, Rodriguez, Laura, Galindo Ramirez, Fabian, De Siati, Romolo Daniele, Santarelli, Rosa Maria, Arslan, Edoardo, Bortolozzi, Mario, Chiorini, John A., Mammano, Fabio

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OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation per Santarelli, Rosamaria, Rossi, Roberta, Scimemi, Pietro, Cama, Elona, Valentino, Maria Lucia, La Morgia, Chiara, Caporali, Leonardo, Liguori, Rocco, Magnavita, Vincenzo, Monteleone, Anna, Biscaro, Ariella, Arslan, Edoardo, Carelli, Valerio

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The Novel PMCA2 Pump Mutation Tommy Impairs Cytosolic Calcium Clearance in Hair Cells and Links to Deafness in Mice per Bortolozzi, Mario, Brini, Marisa, Parkinson, Nick, Crispino, Giulia, Scimemi, Pietro, De Siati, Romolo Daniele, Di Leva, Francesca, Parker, Andrew, Ortolano, Saida, Arslan, Edoardo, Brown, Steve D., Carafoli, Ernesto, Mammano, Fabio

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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 per Schütz, Melanie, Scimemi, Pietro, Majumder, Paromita, De Siati, Romolo Daniele, Crispino, Giulia, Rodriguez, Laura, Bortolozzi, Mario, Santarelli, Rosamaria, Seydel, Anke, Sonntag, Stephan, Ingham, Neil, Steel, Karen P., Willecke, Klaus, Mammano, Fabio

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Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca(2+) signaling and high-frequency hearing acquisition per Rodriguez, Laura, Simeonato, Elena, Scimemi, Pietro, Anselmi, Fabio, Calì, Bianca, Crispino, Giulia, Ciubotaru, Catalin D., Bortolozzi, Mario, Ramirez, Fabian Galindo, Majumder, Paromita, Arslan, Edoardo, De Camilli, Pietro, Pozzan, Tullio, Mammano, Fabio

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Novel Pathogenic Variants in PJVK, the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory Neuropathy Spectrum Disorder per Domínguez-Ruiz, María, Rodríguez-Ballesteros, Montserrat, Gandía, Marta, Gómez-Rosas, Elena, Villamar, Manuela, Scimemi, Pietro, Mancini, Patrizia, Rendtorff, Nanna D., Moreno-Pelayo, Miguel A., Tranebjaerg, Lisbeth, Medà, Carme, Santarelli, Rosamaria, del Castillo, Ignacio

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Speech Perception Changes in the Acoustically Aided, Nonimplanted Ear after Cochlear Implantation: A Multicenter Study per Svirsky, Mario A., Neuman, Arlene C., Neukam, Jonathan D., Lavender, Annette, Miller, Margaret K., Aaron, Ksenia A., Skarzynski, Piotr H., Cywka, Katarzyna B., Skarzynski, Henryk, Truy, Eric, Seldran, Fabien, Hermann, Ruben, Govaerts, Paul, De Ceulaer, Geert, Bergeron, Francois, Hotton, Matthieu, Moran, Michelle, Dowell, Richard C., Goffi-Gomez, Maria Valeria Schmidt, Magalhães, Ana Tereza de Matos, Santarelli, Rosamaria, Scimemi, Pietro

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