Michela Ripolone (M Ripolone)

Scopus Author ID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 19

Top Venues

International journal of molecular sciences

Journal of personalized medicine

Brain sciences

Neuropathology and applied neurobiology

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico Jun 15 2009

Italy

Biologo PhD :: UOD Malattie Neuromuscolari e Rare

Publications

Daniela Piga, Simona Zanotti, Michela Ripolone, Laura Napoli, Patrizia Ciscato, Sara Gibertini, Lorenzo Maggi, Francesco Fortunato, Rigamonti Andrea, Dario Ronchi, Giacomo Pietro Comi, Stefania P Corti, Monica Sciacco
Association between ZASP/LDB3 Pro26Ser and Inclusion Body Myopathy. International journal of molecular sciences 25 (12) (2024)
Daniela Piga, Simona Zanotti, Michela Ripolone, Laura Napoli, Patrizia Ciscato, Sara Gibertini, Lorenzo Maggi, Francesco Fortunato, Rigamonti Andrea, Dario Ronchi, Giacomo Pietro Comi, Stefania P Corti, Monica Sciacco
Association between ZASP/LDB3 Pro26Ser and Inclusion Body Myopathy. International journal of molecular sciences 25 (12) (2024)
Daniela Piga, Simona Zanotti, Michela Ripolone, Laura Napoli, Patrizia Ciscato, Sara Gibertini, Lorenzo Maggi, Francesco Fortunato, Rigamonti Andrea, Dario Ronchi, Giacomo Pietro Comi, Stefania P Corti, Monica Sciacco
Association between ZASP/LDB3 Pro26Ser and Inclusion Body Myopathy. International journal of molecular sciences 25 (12) (2024)
Simona Zanotti, Francesca Magri, Sabrina Salani, Laura Napoli, Michela Ripolone, Dario Ronchi, Francesco Fortunato, Patrizia Ciscato, Daniele Velardo, Maria Grazia D'Angelo, Francesca Gualandi, Vincenzo Nigro, Monica Sciacco, Stefania Corti, Giacomo Pietro Comi, Daniela Piga
Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes. International journal of molecular sciences 24 (6) (2023)
Dario Ronchi, Manuela Garbellini, Francesca Magri, Francesca Menni, Megi Meneri, Maria Francesca Bedeschi, Robertino Dilena, Valeria Cecchetti, Irene Picciolli, Francesca Furlan, Valentina Polimeni, Sabrina Salani, Laura Pezzoli, Francesco Fortunato, Matteo Bellini, Daniela Piga, Michela Ripolone, Simona Zanotti, Laura Napoli, Patrizia Ciscato, Monica Sciacco, Giovanna Mangili, Fabio Mosca, Stefania Corti, Maria Iascone, Giacomo Pietro Comi
A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy. European journal of human genetics : EJHG (2023)
Francesca Magri, Laura Napoli, Michela Ripolone, Patrizia Ciscato, Maurizio Moggio, Stefania P Corti, Giacomo Pietro Comi, Monica Sciacco, Simona Zanotti
The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls. International journal of molecular sciences 24 (24) (2023)
Michela Ripolone, Simona Zanotti, Laura Napoli, Dario Ronchi, Patrizia Ciscato, Giacomo Pietro Comi, Maurizio Moggio, Monica Sciacco
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization. Journal of personalized medicine 13 (1) (2023)
Michela Ripolone, Simona Zanotti, Laura Napoli, Dario Ronchi, Patrizia Ciscato, Giacomo Pietro Comi, Maurizio Moggio, Monica Sciacco
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization. Journal of personalized medicine 13 (1) (2023)
Francesca Magri, Laura Napoli, Michela Ripolone, Patrizia Ciscato, Maurizio Moggio, Stefania P Corti, Giacomo Pietro Comi, Monica Sciacco, Simona Zanotti
The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls. International journal of molecular sciences 24 (24) (2023)
Simona Zanotti, Michela Ripolone, Laura Napoli, Daniele Velardo, Sabrina Salani, Patrizia Ciscato, Silvia Giuliana Priori, Deni Kukavica, Andrea Mazzanti, Luca Diamanti, Elisa Vegezzi, Maurizio Moggio, Stefania Corti, Giacomo Comi, Monica Sciacco
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in Phospholamban Gene. Cells 12 (10) (2023)
Simona Zanotti, Francesca Magri, Sabrina Salani, Laura Napoli, Michela Ripolone, Dario Ronchi, Francesco Fortunato, Patrizia Ciscato, Daniele Velardo, Maria Grazia D'Angelo, Francesca Gualandi, Vincenzo Nigro, Monica Sciacco, Stefania Corti, Giacomo Pietro Comi, Daniela Piga
Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes. International journal of molecular sciences 24 (6) (2023)
Carola Rita Ferrari Aggradi, Martina Rimoldi, Gloria Romagnoli, Daniele Velardo, Megi Meneri, Davide Iacobucci, Michela Ripolone, Laura Napoli, Patrizia Ciscato, Maurizio Moggio, Giacomo Pietro Comi, Dario Ronchi, Stefania P Corti, Elena Abati
Lafora Disease: A Case Report and Evolving Treatment Advancements. Brain sciences 13 (12) (2023)
Simona Zanotti, Francesca Magri, Sabrina Salani, Laura Napoli, Michela Ripolone, Dario Ronchi, Francesco Fortunato, Patrizia Ciscato, Daniele Velardo, Maria Grazia D'Angelo, Francesca Gualandi, Vincenzo Nigro, Monica Sciacco, Stefania Corti, Giacomo Pietro Comi, Daniela Piga
Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes. International journal of molecular sciences 24 (6) (2023)
Michela Ripolone, Simona Zanotti, Laura Napoli, Dario Ronchi, Patrizia Ciscato, Giacomo Pietro Comi, Maurizio Moggio, Monica Sciacco
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization. Journal of personalized medicine 13 (1) (2023)
Carola Rita Ferrari Aggradi, Martina Rimoldi, Gloria Romagnoli, Daniele Velardo, Megi Meneri, Davide Iacobucci, Michela Ripolone, Laura Napoli, Patrizia Ciscato, Maurizio Moggio, Giacomo Pietro Comi, Dario Ronchi, Stefania P Corti, Elena Abati
Lafora Disease: A Case Report and Evolving Treatment Advancements. Brain sciences 13 (12) (2023)
Michela Ripolone, Simona Zanotti, Laura Napoli, Dario Ronchi, Patrizia Ciscato, Giacomo Pietro Comi, Maurizio Moggio, Monica Sciacco
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization. Journal of personalized medicine 13 (1) (2023)
Michela Ripolone, Daniele Velardo, Stefania Mondello, Simona Zanotti, Francesca Magri, Elisa Minuti, Sara Cazzaniga, Francesco Fortunato, Patrizia Ciscato, Francesca Tiberio, Monica Sciacco, Maurizio Moggio, Paolo Bettica, Giacomo P Comi
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy. Acta neuropathologica communications 10 (1) (2022)
Michela Ripolone, Valeria Lucchini, Dario Ronchi, Gigliola Fagiolari, Andreina Bordoni, Francesco Fortunato, Stefania Mondello, Sara Bonato, Mirella Meregalli, Yvan Torrente, Stefania Corti, Giacomo P Comi, Maurizio Moggio, Monica Sciacco
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1. Journal of neuroscience research 96 (9) (2019)
Michela Ripolone, R Violano, D Ronchi, S Mondello, A Nascimbeni, I Colombo, G Fagiolari, A Bordoni, F Fortunato, V Lucchini, S Saredi, M Filosto, O Musumeci, P Tonin, T Mongini, S Previtali, L Morandi, C Angelini, M Mora, M Sandri, M Sciacco, A Toscano, G P Comi, M Moggio
Effects of short-to-long term enzyme replacement therapy (ERT) on skeletal muscle tissue in late onset Pompe disease (LOPD). Neuropathology and applied neurobiology 44 (5) (2017)

Michela Ripolone.css-eqlu8i{font-size:small;padding-left:4px;} (M Ripolone)

Publication Activity (10 Years)

Top Topics

Top Venues

Michela Ripolone (M Ripolone)