Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sara, Massucco"'
Autor:
Sara Massucco, Cristina Schenone, Elena Faedo, Chiara Gemelli, Emilia Bellone, Lucio Marinelli, Davide Pareyson, Chiara Pisciotta, Tiziana Mongini, Angelo Schenone, Marina Grandis
Publikováno v:
Frontiers in Neurology, Vol 14 (2024)
Sleep-disordered breathing has been reported in Charcot–Marie–Tooth disease (CMT) type 1A in association with diaphragmatic weakness and sleep apnea syndrome, mainly of the obstructive type (OSA). Improvement has been observed not only in sleep q
Externí odkaz:
https://doaj.org/article/ecc7757579ef4f69bbec7debe720e4d1
Autor:
Laura Mori, Cristina Schenone, Filippo Cotellessa, Marta Ponzano, Alessia Aiello, Maria Lagostina, Sara Massucco, Lucio Marinelli, Marina Grandis, Carlo Trompetto, Angelo Schenone
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Charcot-Marie-Tooth (CMT) patients present mainly lower limbs disability, with slowly progressive distal muscle weakness and atrophy, but hands impairment is a relevant problem affecting the quality of life (QoL). The evaluation of the upper limb is
Externí odkaz:
https://doaj.org/article/8d0e1413f2474d019e9d6dd6ff8262fa
Autor:
Elena Scarsi, Sara Massucco, Pilar M. Ferraro, Arianna Cella, Stefano G. Grisanti, Andrea Assini, Alessandro Beronio, Fabio Della Cava, Chiara Gemelli, Fabio Bandini, Carlo Serrati, Massimo Del Sette, Angelo Schenone, Luana Benedetti, Valeria Prada, Marina Grandis
Publikováno v:
Life, Vol 13, Iss 4, p 1064 (2023)
We evaluated 13 patients affected by myasthenia gravis (MG) who had coronavirus disease 2019 (COVID-19) before vaccination and 14 myasthenic patients who contracted severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) infection after vaccinat
Externí odkaz:
https://doaj.org/article/ac211d62f2df42d0b0abdfe073399c3a
Autor:
Chiara Gemelli, Alessandro Geroldi, Sara Massucco, Lucia Trevisan, Ilaria Callegari, Lucio Marinelli, Giulia Ursino, Mehrnaz Hamedani, Giulia Mennella, Silvia Stara, Giovanni Maggi, Laura Mori, Cristina Schenone, Fabio Gotta, Serena Patrone, Alessia Mammi, Paola Origone, Valeria Prada, Lucilla Nobbio, Paola Mandich, Angelo Schenone, Emilia Bellone, Marina Grandis
Publikováno v:
Life, Vol 12, Iss 3, p 402 (2022)
Charcot–Marie–Tooth (CMT) disease is the most commonly inherited neurological disorder. This study includes patients affected by CMT during regular follow-ups at the CMT clinic in Genova, a neuromuscular university center in the northwest of Ital
Externí odkaz:
https://doaj.org/article/6a0ea7e07bf84bfa957c4bd6181b2c97
Autor:
Valeria Prada, Sara Massucco, Consuelo Venturi, Alessandro Geroldi, Emilia Bellone, Paola Mandich, Michele Minuto, Emanuela Varaldo, Giovanni Mancardi, Marina Grandis, Angelo Schenone
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Nerve biopsy represents the conclusive step in the diagnostic work-up of peripheral neuropathies, and its diagnostic yield is still debated. The aim of this study is to consider the impact of nerve biopsy on reaching a useful diagnosis in different p
Externí odkaz:
https://doaj.org/article/ee90335d366a48b69ffe18b348374fe0
Autor:
Marco Luigetti, Marina Romozzi, Giulia Bisogni, Davide Cardellini, Tiziana Cavallaro, Andrea Di Paolantonio, Gian Maria Fabrizi, Silvia Fenu, Luca Gentile, Marina Grandis, Gianluca Marucci, Sara Massucco, Anna Mazzeo, Davide Pareyson, Angela Romano, Massimo Russo, Angelo Schenone, Matteo Tagliapietra, Stefano Tozza, Giuseppe Vita, Mario Sabatelli
Publikováno v:
Brain Sciences, Vol 10, Iss 11, p 780 (2020)
Pathological evidence of amyloid on nerve biopsy has been the gold standard for diagnosis in hereditary transthyretin amyloidosis polyneuropathy (hATTR-PN) for a long time. In this article, we reviewed the pathological findings of a large series of s
Externí odkaz:
https://doaj.org/article/17201db1317b444c851ed8859b025690
Autor:
Magliano, Lorenza, Obici, Laura, Sforzini, Claudia, Mazzeo, Anna, Russo, Massimo, Cappelli, Francesco, Fenu, Silvia, Luigetti, Marco, Tagliapietra, Matteo, Gemelli, Chiara, Leonardi, Luca, Tozza, Stefano, Pradotto, Luca Guglielmo, Citarelli, Giulia, Mauro, Alessandro, Manganelli, Fiore, Antonini, Giovanni, Grandis, Marina, Fabrizi, Gian Maria, Sabatelli, Mario, Pareyson, Davide, Perfetto, Federico, Merlini, Giampaolo, Vita, Giuseppe, Giulia, Bisogni, Daniela, Calabrese, Davide, Cardellini, Silvia, Casagrande, Tiziana, Cavallaro, Eleonora Di Buduo, Andrea Di Paolantonio, Gentile, Luca, Graceffa, Anita Maria Stella, Sara, Massucco, Alessandra, Milesi, Stefania, Morino, Roberta, Mussinelli, Paola, Saveri, Daniele, Severi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Hereditary transthyretin amyloidosis (hATTR), alias ATTR variant (ATTRv) is a severe and disabling disease causing sensory and motor neuropathy, autonomic dysfunction, and cardiomyopathy. The progressive decline of patient’s functional a
Autor:
Gianluca Marucci, Marina Grandis, Davide Pareyson, Anna Mazzeo, Andrea Di Paolantonio, Giuseppe Vita, Stefano Tozza, Marina Romozzi, Angela Romano, Tiziana Cavallaro, Marco Luigetti, Luca Gentile, Matteo Tagliapietra, Angelo Schenone, Davide Cardellini, Massimo Russo, Silvia Fenu, Giulia Bisogni, Mario Sabatelli, Sara Massucco, Gian Maria Fabrizi
Publikováno v:
Brain Sciences; Volume 10; Issue 11; Pages: 780
Brain Sciences
Brain Sciences, Vol 10, Iss 780, p 780 (2020)
Brain Sciences
Brain Sciences, Vol 10, Iss 780, p 780 (2020)
Pathological evidence of amyloid on nerve biopsy has been the gold standard for diagnosis in hereditary transthyretin amyloidosis polyneuropathy (hATTR-PN) for a long time. In this article, we reviewed the pathological findings of a large series of s