Resultats de la cerca - Tozza, Stefano
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One-year follow up of three Italian patients with Duchenne muscular dystrophy treated with ataluren: is earlier better? per Ruggiero, Lucia, Iodice, Rosa, Esposito, Marcello, Dubbioso, Raffaele, Tozza, Stefano, Vitale, Floriana, Santoro, Lucio, Manganelli, Fiore
Publicat 2018Text -
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Primary Progressive Multiple Sclerosis Under Anti-TNFα Treatment: A Case Report per Iovino, Aniello, Aruta, Francesco, Dubbioso, Raffaele, Ruggiero, Lucia, Tozza, Stefano, Spina, Emanuele, Manganelli, Fiore, Iodice, Rosa
Publicat 2020Text -
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Microstructural Changes in Motor Functional Conversion Disorder: Multimodal Imaging Approach on a Case per Longarzo, Mariachiara, Cavaliere, Carlo, Mele, Giulia, Tozza, Stefano, Tramontano, Liberatore, Alfano, Vincenzo, Aiello, Marco, Salvatore, Marco, Grossi, Dario
Publicat 2020Text -
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In vivo evidence of cortical amyloid deposition in the adult form of Niemann Pick type C per Esposito, Marcello, Dubbioso, Raffaele, Tozza, Stefano, Iodice, Rosa, Aiello, Marco, Nicolai, Emanuele, Cavaliere, Carlo, Salvatore, Marco, Santoro, Lucio, Manganelli, Fiore
Publicat 2019Text -
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The neuropathy in hereditary transthyretin amyloidosis: A narrative review per Tozza, Stefano, Severi, Daniele, Spina, Emanuele, Iovino, Aniello, Aruta, Francesco, Ruggiero, Lucia, Dubbioso, Raffaele, Iodice, Rosa, Nolano, Maria, Manganelli, Fiore
Publicat 2021Text -
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Brain Plasticity in Charcot-Marie-Tooth Type 1A Patients? A Combined Structural and Diffusion MRI Study per Pontillo, Giuseppe, Dubbioso, Raffaele, Cocozza, Sirio, Tozza, Stefano, Severi, Daniele, Iodice, Rosa, Tedeschi, Enrico, Elefante, Andrea, Brunetti, Arturo, Manganelli, Fiore, Quarantelli, Mario
Publicat 2020Text -
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How to manage with telemedicine people with neuromuscular diseases? per Spina, Emanuele, Trojsi, Francesca, Tozza, Stefano, Iovino, Aniello, Iodice, Rosa, Passaniti, Carla, Abbadessa, Gianmarco, Bonavita, Simona, Leocani, Letizia, Tedeschi, Gioacchino, Manganelli, Fiore, Lavorgna, Luigi
Publicat 2021Text -
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Correction to: How to manage with telemedicine people with neuromuscular diseases? per Spina, Emanuele, Trojsi, Francesca, Tozza, Stefano, Iovino, Aniello, Iodice, Rosa, Passaniti, Carla, Abbadessa, Gianmarco, Bonavita, Simona, Leocani, Letizia, Tedeschi, Gioacchino, Manganelli, Fiore, Lavorgna, Luigi
Publicat 2021Text -
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The impact of symptoms on daily life as perceived by patients with Charcot-Marie-Tooth type 1A disease per Tozza, Stefano, Bruzzese, Dario, Severi, Daniele, Spina, Emanuele, Iodice, Rosa, Ruggiero, Lucia, Dubbioso, Raffaele, Iovino, Aniello, Aruta, Francesco, Nolano, Maria, Santoro, Lucio, Manganelli, Fiore
Publicat 2021Text -
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A compound score to screen patients with hereditary transthyretin amyloidosis per Tozza, Stefano, Severi, Daniele, Spina, Emanuele, Di Paolantonio, Andrea, Iovino, Aniello, Guglielmino, Valeria, Aruta, Francesco, Nolano, Maria, Sabatelli, Mario, Santoro, Lucio, Luigetti, Marco, Manganelli, Fiore
Publicat 2022Text -
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A Novel CAPN1 Mutation Causes a Pure Hereditary Spastic Paraplegia in an Italian Family per Cotti Piccinelli, Stefano, Bassi, Maria T., Citterio, Andrea, Manganelli, Fiore, Tozza, Stefano, Santorelli, Filippo M., Gallo Cassarino, Serena, Caria, Filomena, Baldelli, Enrico, Galvagni, Anna, Santoro, Lucio, Padovani, Alessandro, Filosto, Massimiliano
Publicat 2019Text -
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Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy “in disguise” per Grandis, Marina, Geroldi, Alessandro, Gulli, Rossella, Manganelli, Fiore, Gotta, Fabio, Lamp, Merit, Origone, Paola, Trevisan, Lucia, Gemelli, Chiara, Fabbri, Sabrina, Schenone, Angelo, Tozza, Stefano, Santoro, Lucio, Bellone, Emilia, Mandich, Paola
Publicat 2018Text -
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Novel mutations in dystonin provide clues to the pathomechanisms of HSAN-VI per Manganelli, Fiore, Parisi, Silvia, Nolano, Maria, Tao, Feifei, Paladino, Simona, Pisciotta, Chiara, Tozza, Stefano, Nesti, Claudia, Rebelo, Adriana P., Provitera, Vincenzo, Santorelli, Filippo M., Shy, Michael E., Russo, Tommaso, Zuchner, Stephan, Santoro, Lucio
Publicat 2017Text -
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Diagnosis and Management of Type 1 Sialidosis: Clinical Insights from Long-Term Care of Four Unrelated Patients per Coppola, Antonietta, Ianniciello, Marta, Vanli-Yavuz, Ebru N., Rossi, Settimio, Simonelli, Francesca, Castellotti, Barbara, Esposito, Marcello, Tozza, Stefano, Troisi, Serena, Bellofatto, Marta, Ugga, Lorenzo, Striano, Salvatore, D’Amico, Alessandra, Baykan, Betul, Striano, Pasquale, Bilo, Leonilda
Publicat 2020Text -
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Telemedicine application to headache: a critical review per Spina, Emanuele, Tedeschi, Gioacchino, Russo, Antonio, Trojsi, Francesca, Iodice, Rosa, Tozza, Stefano, Iovino, Aniello, Iodice, Francesco, Abbadessa, Gianmarco, di Lorenzo, Francesco, Miele, Giuseppina, Maida, Elisabetta, Cerullo, Giovanni, Sparaco, Maddalena, Silvestro, Marcello, Leocani, Letizia, Bonavita, Simona, Manganelli, Fiore, Lavorgna, Luigi
Publicat 2022Text -
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Real‐life experience with inotersen in hereditary transthyretin amyloidosis with late‐onset phenotype: Data from an early‐access program in Italy per Luigetti, Marco, Antonini, Giovanni, Di Paolantonio, Andrea, Gentile, Luca, Grandis, Marina, Leonardi, Luca, Lozza, Alessandro, Manganelli, Fiore, Mazzeo, Anna, Mussinelli, Roberta, My, Filomena, Obici, Laura, Maria Pennisi, Elena, Romozzi, Marina, Russo, Massimo, Sabatelli, Mario, Salvalaggio, Alessandro, Tagliapietra, Matteo, Tozza, Stefano
Publicat 2022Text -
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hATTR Pathology: Nerve Biopsy Results from Italian Referral Centers per Luigetti, Marco, Romozzi, Marina, Bisogni, Giulia, Cardellini, Davide, Cavallaro, Tiziana, Di Paolantonio, Andrea, Fabrizi, Gian Maria, Fenu, Silvia, Gentile, Luca, Grandis, Marina, Marucci, Gianluca, Massucco, Sara, Mazzeo, Anna, Pareyson, Davide, Romano, Angela, Russo, Massimo, Schenone, Angelo, Tagliapietra, Matteo, Tozza, Stefano, Vita, Giuseppe, Sabatelli, Mario
Publicat 2020Text