Advances in spinal muscular atrophy therapeutics by Valeria Parente, Stefania Corti

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Adeno-Associated Virus (AAV)-Mediated Gene Therapy for Duchenne Muscular Dystrophy: The Issue of Transgene Persistence by Arianna Manini, Elena Abati, Andi Nuredini, Stefania Corti, Stefania Corti, Giacomo Pietro Comi, Giacomo Pietro Comi

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Advancing Drug Discovery for Neurological Disorders Using iPSC-Derived Neural Organoids by Gianluca Costamagna, Giacomo Pietro Comi, Stefania Corti

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Advancing Stroke Research on Cerebral Thrombi with Omic Technologies by Gianluca Costamagna, Sara Bonato, Stefania Corti, Megi Meneri

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Case report: Clinical and molecular characterization of two siblings affected by Brody myopathy by Daniele Velardo, Sara Antognozzi, Martina Rimoldi, Serena Pagliarani, Filippo Cogiamanian, Sergio Barbieri, Stefania Corti, Stefania Corti, Giacomo Pietro Comi, Giacomo Pietro Comi, Dario Ronchi

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Glial cells involvement in spinal muscular atrophy: Could SMA be a neuroinflammatory disease? by Elena Abati, Gaia Citterio, Nereo Bresolin, Giacomo P. Comi, Stefania Corti

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Perspectives on hiPSC-Derived Muscle Cells as Drug Discovery Models for Muscular Dystrophies by Elena Abati, Emanuele Sclarandi, Giacomo Pietro Comi, Valeria Parente, Stefania Corti

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New Insights into Cerebral Vessel Disease Landscapes at Single-Cell Resolution: Pathogenetic and Therapeutic Perspectives by Megi Meneri, Sara Bonato, Delia Gagliardi, Giacomo P. Comi, Stefania Corti

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Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature by Delia Gagliardi, Eleonora Mauri, Francesca Magri, Daniele Velardo, Megi Meneri, Elena Abati, Roberta Brusa, Irene Faravelli, Daniela Piga, Dario Ronchi, Fabio Triulzi, Lorenzo Peverelli, Monica Sciacco, Nereo Bresolin, Nereo Bresolin, Giacomo Pietro Comi, Giacomo Pietro Comi, Stefania Corti, Stefania Corti, Stefania Corti, Alessandra Govoni, Alessandra Govoni

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Growing Evidence about the Relationship between Vessel Dissection and Scuba Diving by Simona Brajkovic, Giulietta Riboldi, Alessandra Govoni, Stefania Corti, Nereo Bresolin, Giacomo Pietro Comi

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Newly Diagnosed Hepatic Encephalopathy Presenting as Non-convulsive Status Epilepticus: A Case Report and Literature Review by Marco Olivero, Delia Gagliardi, Delia Gagliardi, Gianluca Costamagna, Daniele Velardo, Francesca Magri, Fabio Triulzi, Giorgio Conte, Giacomo P. Comi, Giacomo P. Comi, Stefania Corti, Stefania Corti, Megi Meneri, Megi Meneri

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Case report: A novel patient presenting TRIM32-related limb-girdle muscular dystrophy by Martina Rimoldi, Gloria Romagnoli, Francesca Magri, Sara Antognozzi, Claudia Cinnante, Elena Saccani, Patrizia Ciscato, Simona Zanotti, Daniele Velardo, Stefania Corti, Stefania Corti, Giacomo Pietro Comi, Giacomo Pietro Comi, Dario Ronchi, Dario Ronchi

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Direct Reprogramming of Adult Somatic Cells into other Lineages: Past Evidence and Future Perspectives by Monica Nizzardo, Chiara Simone, Marianna Falcone, Giulietta Riboldi, Giacomo P. Comi, Nereo Bresolin, Stefania Corti

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Stormorken Syndrome Caused by a p.R304W STIM1 Mutation: The First Italian Patient and a Review of the Literature by Oscar Borsani, Daniela Piga, Stefania Costa, Alessandra Govoni, Francesca Magri, Andrea Artoni, Claudia M. Cinnante, Gigliola Fagiolari, Patrizia Ciscato, Maurizio Moggio, Nereo Bresolin, Nereo Bresolin, Giacomo P. Comi, Giacomo P. Comi, Stefania Corti, Stefania Corti

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Targeting PTB for Glia-to-Neuron Reprogramming In Vitro and In Vivo for Therapeutic Development in Neurological Diseases by Matilde Contardo, Roberta De Gioia, Delia Gagliardi, Giacomo Pietro Comi, Linda Ottoboni, Monica Nizzardo, Stefania Corti

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Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant by Martina Rimoldi, Francesca Magri, Sara Antognozzi, Michela Ripolone, Sabrina Salani, Daniela Piga, Letizia Bertolasi, Simona Zanotti, Patrizia Ciscato, Francesco Fortunato, Maurizio Moggio, Stefania Corti, Stefania Corti, Giacomo Pietro Comi, Giacomo Pietro Comi, Dario Ronchi, Dario Ronchi

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Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions by Arianna Manini, Leonardo Caporali, Megi Meneri, Megi Meneri, Simona Zanotti, Daniela Piga, Ignazio Giuseppe Arena, Stefania Corti, Stefania Corti, Antonio Toscano, Giacomo Pietro Comi, Giacomo Pietro Comi, Olimpia Musumeci, Valerio Carelli, Valerio Carelli, Dario Ronchi, Dario Ronchi

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Early Findings in Neonatal Cases of RYR1–Related Congenital Myopathies by Eleonora Mauri, Daniela Piga, Alessandra Govoni, Roberta Brusa, Serena Pagliarani, Michela Ripolone, Robertino Dilena, Claudia Cinnante, Monica Sciacco, Denise Cassandrini, Vincenzo Nigro, Nereo Bresolin, Nereo Bresolin, Stefania Corti, Stefania Corti, Giacomo P. Comi, Giacomo P. Comi, Francesca Magri

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Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort Study by Delia Gagliardi, Delia Gagliardi, Irene Faravelli, Manuel Alfredo Podestà, Roberta Brusa, Eleonora Mauri, Domenica Saccomanno, Alessio Di Fonzo, Sara Bonato, Elio Scarpini, Elio Scarpini, Nereo Bresolin, Nereo Bresolin, Giacomo Pietro Comi, Giacomo Pietro Comi, Stefania Corti, Stefania Corti

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Case report: A novel ACTA1 variant in a patient with nemaline rods and increased glycogen deposition by Daniela Piga, Martina Rimoldi, Martina Rimoldi, Francesca Magri, Simona Zanotti, Laura Napoli, Michela Ripolone, Serena Pagliarani, Patrizia Ciscato, Daniele Velardo, Adele D’Amico, Enrico Bertini, Giacomo Pietro Comi, Giacomo Pietro Comi, Dario Ronchi, Dario Ronchi, Stefania Corti, Stefania Corti

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