Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Stefania Marcuzzo"'
Autor:
Claudia Malacarne, Eleonora Giagnorio, Cristina Chirizzi, Marco Cattaneo, Fulvia Saraceno, Paola Cavalcante, Silvia Bonanno, Renato Mantegazza, Victoria Moreno-Manzano, Giuseppe Lauria, Pierangelo Metrangolo, Francesca Baldelli Bombelli, Stefania Marcuzzo
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 173, Iss , Pp 116380- (2024)
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease affecting motor neurons. Considerable evidence indicates that early skeletal muscle atrophy plays a crucial role in the disease pathogenesis, leading to an altered muscle-
Externí odkaz:
https://doaj.org/article/c2b268c982fe4b4499a99e37c70e138f
Autor:
Mirna Andelic, Margherita Marchi, Stefania Marcuzzo, Raffaella Lombardi, Catharina G. Faber, Giuseppe Lauria, Erika Salvi
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 31, Iss , Pp 101116- (2023)
Archived specimens, taken by standardized procedures in clinical practice, represent a valuable resource in translational medicine. Their use in retrospective molecular-based studies could provide disease and therapy predictors. Microfluidic array is
Externí odkaz:
https://doaj.org/article/61ea216ce05444ac8769e14814f332d8
Autor:
Nina Bono, Giulio Saroglia, Stefania Marcuzzo, Eleonora Giagnorio, Giuseppe Lauria, Elena Rosini, Luigi De Nardo, Athanassia Athanassiou, Gabriele Candiani, Giovanni Perotto
Publikováno v:
Journal of Materials Science: Materials in Medicine, Vol 34, Iss 1, Pp 1-12 (2022)
Abstract Cell microencapsulation has been utilized for years as a means of cell shielding from the external environment while facilitating the transport of gases, general metabolites, and secretory bioactive molecules at once. In this light, hydrogel
Externí odkaz:
https://doaj.org/article/b1716cc25ebd493395be18477fcad997
Autor:
Silvia Bonanno, Paola Cavalcante, Erika Salvi, Eleonora Giagnorio, Claudia Malacarne, Marco Cattaneo, Francesca Andreetta, Anna Venerando, Viviana Pensato, Cinzia Gellera, Riccardo Zanin, Maria Teresa Arnoldi, Claudia Dosi, Renato Mantegazza, Riccardo Masson, Lorenzo Maggi, Stefania Marcuzzo
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 16 (2022)
Background and objectivesMultisystem involvement in spinal muscular atrophy (SMA) is gaining prominence since different therapeutic options are emerging, making the way for new SMA phenotypes and consequent challenges in clinical care. Defective immu
Externí odkaz:
https://doaj.org/article/2c3d2def91f54c2e9bdb62f8366a15f0
Autor:
Eleonora Giagnorio, Claudia Malacarne, Paola Cavalcante, Letizia Scandiffio, Marco Cattaneo, Viviana Pensato, Cinzia Gellera, Nilo Riva, Angelo Quattrini, Eleonora Dalla Bella, Giuseppe Lauria, Renato Mantegazza, Silvia Bonanno, Stefania Marcuzzo
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 5, p 4610 (2023)
Amyotrophic lateral sclerosis (ALS) is characterized by the progressive, irreversible loss of upper and lower motor neurons (UMNs, LMNs). MN axonal dysfunctions are emerging as relevant pathogenic events since the early ALS stages. However, the exact
Externí odkaz:
https://doaj.org/article/b8e0f57026df4579a4525a3b24ba198f
Autor:
Nicola Iacomino, Letizia Scandiffio, Fabio Conforti, Erika Salvi, Maria Cristina Tarasco, Federica Bortone, Stefania Marcuzzo, Ornella Simoncini, Francesca Andreetta, Daniela Pistillo, Emanuele Voulaz, Marco Alloisio, Carlo Antozzi, Renato Mantegazza, Tommaso Martino De Pas, Paola Cavalcante
Publikováno v:
Biomedicines, Vol 11, Iss 3, p 732 (2023)
The thymus is widely recognized as an immunological niche where autoimmunity against the acetylcholine receptor (AChR) develops in myasthenia gravis (MG) patients, who mostly present thymic hyperplasia and thymoma. Thymoma-associated MG is frequently
Externí odkaz:
https://doaj.org/article/fcd0925d934041828e69ee71fe439a29
Autor:
Federica Bortone, Letizia Scandiffio, Stefania Marcuzzo, Silvia Bonanno, Rita Frangiamore, Teresio Motta, Carlo Antozzi, Renato Mantegazza, Paola Cavalcante, Pia Bernasconi
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Toll-like receptor (TLR)-mediated innate immune responses are critically involved in the pathogenesis of myasthenia gravis (MG), an autoimmune disorder affecting neuromuscular junction mainly mediated by antiacetylcholine receptor antibodies. Conside
Externí odkaz:
https://doaj.org/article/7ec59aeab16a48b0a1f55b188fc798fc
Autor:
Federica Rey, Stefania Marcuzzo, Silvia Bonanno, Matteo Bordoni, Toniella Giallongo, Claudia Malacarne, Cristina Cereda, Gian Vincenzo Zuccotti, Stephana Carelli
Publikováno v:
Biomedicines, Vol 9, Iss 7, p 809 (2021)
Amyotrophic Lateral Sclerosis (ALS) is a devastating neurodegenerative disease caused in 10% of cases by inherited mutations considered “familial”. An ever-increasing amount of evidence is showing a fundamental role for RNA metabolism in ALS path
Externí odkaz:
https://doaj.org/article/7c2cf1cb136a4afeba7938f6a87cdf50
Autor:
Claudia Malacarne, Mariarita Galbiati, Eleonora Giagnorio, Paola Cavalcante, Franco Salerno, Francesca Andreetta, Cinza Cagnoli, Michela Taiana, Monica Nizzardo, Stefania Corti, Viviana Pensato, Anna Venerando, Cinzia Gellera, Silvia Fenu, Davide Pareyson, Riccardo Masson, Lorenzo Maggi, Eleonora Dalla Bella, Giuseppe Lauria, Renato Mantegazza, Pia Bernasconi, Angelo Poletti, Silvia Bonanno, Stefania Marcuzzo
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 11, p 5673 (2021)
Motor neuron diseases (MNDs) are neurodegenerative disorders characterized by upper and/or lower MN loss. MNDs include amyotrophic lateral sclerosis (ALS), spinal muscular atrophy (SMA), and spinal and bulbar muscular atrophy (SBMA). Despite variabil
Externí odkaz:
https://doaj.org/article/b7c9e05555d94d17af21404c5367ccb5
Autor:
Silvia Bonanno, Stefania Marcuzzo, Claudia Malacarne, Eleonora Giagnorio, Riccardo Masson, Riccardo Zanin, Maria Teresa Arnoldi, Francesca Andreetta, Ornella Simoncini, Anna Venerando, Cinzia Gellera, Chiara Pantaleoni, Renato Mantegazza, Pia Bernasconi, Giovanni Baranello, Lorenzo Maggi
Publikováno v:
Biomedicines, Vol 8, Iss 2, p 21 (2020)
Spinal muscular atrophy (SMA) is an autosomal recessive disorder caused by mutations in survival motor neuron (SMN) 1 gene, resulting in a truncated SMN protein responsible for degeneration of brain stem and spinal motor neurons. The paralogous SMN2
Externí odkaz:
https://doaj.org/article/338fd9188e6942ff9207ee02ff1fb865