Kết quả tìm kiếm - Scimemi, Pietro
- Đang hiển thị 1 - 11 kết quả của 11
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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 Bằng Santarelli, Rosamaria, La Morgia, Chiara, Valentino, Maria Lucia, Barboni, Piero, Monteleone, Anna, Scimemi, Pietro, Carelli, Valerio
Được phát hành 2019Text -
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An audiological perspective on ‘‘Two further patients with Warsaw breakage syndrome. Is a mild phenotype possible?” Bằng Brotto, Davide, Manara, Renzo, Scimemi, Pietro, Sorrentino, Flavia, Montino, Silvia, Maritan, Francesca, Caserta, Ezio, Lovo, Elisa, Martini, Alessandro, Santarelli, Rosamaria, Trevisi, Patrizia
Được phát hành 2020Text -
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BAAV Mediated GJB2 Gene Transfer Restores Gap Junction Coupling in Cochlear Organotypic Cultures from Deaf Cx26Sox10Cre Mice Bằng 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
Được phát hành 2011Text -
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OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation Bằng 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
Được phát hành 2015Text -
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The Novel PMCA2 Pump Mutation Tommy Impairs Cytosolic Calcium Clearance in Hair Cells and Links to Deafness in Mice Bằng 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
Được phát hành 2010Text -
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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 Bằng 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
Được phát hành 2010Text -
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Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca(2+) signaling and high-frequency hearing acquisition Bằng 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
Được phát hành 2012Text -
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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 Bằng 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
Được phát hành 2022Text -
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Speech Perception Changes in the Acoustically Aided, Nonimplanted Ear after Cochlear Implantation: A Multicenter Study Bằng 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
Được phát hành 2020Text