Search Results - Giovanni Meola

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  1. 1

    Editorial: Myopathology of inherited myopathies by Chiara Fiorillo, Edoardo Malfatti, Edoardo Malfatti, Giovanni Meola, Giovanni Meola

    Published in Frontiers in Neurology (2022-08-01)
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  2. 2

    Case report: Sodium and chloride muscle channelopathy coexistence: A complicated phenotype and a challenging diagnosis by Serena Pagliarani, Giovanni Meola, Giovanni Meola, Melania Filareti, Giacomo Pietro Comi, Sabrina Lucchiari

    Published in Frontiers in Neurology (2022-08-01)
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  3. 3

    Rare Disease: Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1 by Marco Alì, Marco Alì, Caterina Beatrice Monti, Luca Melazzini, Rosanna Cardani, Barbara Fossati, Barbara Fossati, Michele Cavalli, Kelvin Chow, Francesco Secchi, Francesco Secchi, Giovanni Meola, Giovanni Meola, Giovanni Meola, Francesco Sardanelli, Francesco Sardanelli

    Published in Frontiers in Neurology (2020-03-01)
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  4. 4

    Case report: Dihydropyridine receptor (CACNA1S) congenital myopathy, a novel phenotype with early onset periodic paralysis by Samah K. Aburahma, Liqa A. Rousan, Mohammad Shboul, Fabio Biella, Sabrina Lucchiari, Giacomo Pietro Comi, Giacomo Pietro Comi, Giovanni Meola, Giovanni Meola, Serena Pagliarani

    Published in Frontiers in Neurology (2024-02-01)
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  5. 5

    TNNT2 Missplicing in Skeletal Muscle as a Cardiac Biomarker in Myotonic Dystrophy Type 1 but Not in Myotonic Dystrophy Type 2 by Francesca Bosè, Laura Valentina Renna, Barbara Fossati, Barbara Fossati, Giovanni Arpa, Valentina Labate, Valentina Milani, Annalisa Botta, Emanuele Micaglio, Giovanni Meola, Giovanni Meola, Rosanna Cardani

    Published in Frontiers in Neurology (2019-09-01)
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  6. 6

    Cardiac risk and myocardial fibrosis assessment with cardiac magnetic resonance in patients with myotonic dystrophy by Elena Abati, Elena Abati, Claudia Alberti, Valentina Tambè, Anastasia Esseridou, Giacomo Pietro Comi, Giacomo Pietro Comi, Stefania Corti, Stefania Corti, Giovanni Meola, Giovanni Meola, Francesco Secchi, Francesco Secchi

    Published in Frontiers in Neurology (2024-11-01)
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  7. 7

    Aberrant insulin receptor expression is associated with insulin resistance and skeletal muscle atrophy in myotonic dystrophies. by Laura Valentina Renna, Francesca Bosè, Elisa Brigonzi, Barbara Fossati, Giovanni Meola, Rosanna Cardani

    Published in PLoS ONE (2019-01-01)
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  8. 8

    Circulating Irisin Is Reduced in Male Patients with Type 1 and Type 2 Myotonic Dystrophies by Elena Dozio, Elena Passeri, Rosanna Cardani, Stefano Benedini, Carmen Aresta, Rea Valaperta, Massimiliano Corsi Romanelli, Massimiliano Corsi Romanelli, Giovanni Meola, Giovanni Meola, Valeria Sansone, Valeria Sansone, Sabrina Corbetta, Sabrina Corbetta

    Published in Frontiers in Endocrinology (2017-11-01)
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  9. 9

    Transcranial brain parenchyma sonographic findings in patients with myotonic dystrophy type 1 and 2 by Milija Mijajlovic, Ivo Bozovic, Aleksandra Pavlovic, Vidosava Rakocevic-Stojanovic, Sanja Gluscevic, Amalija Stojanovic, Ivana Basta, Giovanni Meola, Stojan Peric

    Published in Heliyon (2024-03-01)
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  10. 10

    Overexpression of CUGBP1 in skeletal muscle from adult classic myotonic dystrophy type 1 but not from myotonic dystrophy type 2. by Rosanna Cardani, Enrico Bugiardini, Laura V Renna, Giulia Rossi, Graziano Colombo, Rea Valaperta, Giuseppe Novelli, Annalisa Botta, Giovanni Meola

    Published in PLoS ONE (2013-01-01)
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  11. 11

    Evaluation of Sleep-Disordered Breathing and Respiratory Dysfunction in Children with Myotonic Dystrophy Type 1—A Retrospective Cross-Sectional Study by Mihail Basa, Jovan Pesovic, Dusanka Savic-Pavicevic, Stojan Peric, Giovanni Meola, Alessandro Amaddeo, Gordana Kovacevic, Slavica Ostojic, Aleksandar Sovtic

    Published in Biomedicines (2025-04-01)
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  12. 12

    Understanding the Impact of Non-Dystrophic Myotonia on Patients and Caregivers: Results from a Burden of Disease Healthcare Survey by Jordi Diaz-Manera, Channa Hewamadduma, Giovanni Meola, Federica Montagnese, Sabrina Sacconi, Philipp von Gallwitz, Ulrike Nowak, Robert Pleticha, Alla Zozulya Weidenfeller

    Published in European Medical Journal (2021-06-01)
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  13. 13

    Case report: Multiple approach analysis in a case of clinically assessed myotonia congenita by Sabrina Lucchiari, Francesco Fortunato, Giovanni Meola, Andrea Mignarri, Serena Pagliarani, Stefania Corti, Stefania Corti, Giacomo P. Comi, Giacomo P. Comi, Dario Ronchi, Dario Ronchi

    Published in Frontiers in Genetics (2024-12-01)
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  14. 14

    Brain Connectomics’ Modification to Clarify Motor and Nonmotor Features of Myotonic Dystrophy Type 1 by Laura Serra, Matteo Mancini, Gabriella Silvestri, Antonio Petrucci, Marcella Masciullo, Barbara Spanò, Mario Torso, Chiara Mastropasqua, Manlio Giacanelli, Carlo Caltagirone, Mara Cercignani, Giovanni Meola, Marco Bozzali

    Published in Neural Plasticity (2016-01-01)
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  15. 15

    RBFOX1 cooperates with MBNL1 to control splicing in muscle, including events altered in myotonic dystrophy type 1. by Roscoe Klinck, Angélique Fourrier, Philippe Thibault, Johanne Toutant, Mathieu Durand, Elvy Lapointe, Marie-Laure Caillet-Boudin, Nicolas Sergeant, Geneviève Gourdon, Giovanni Meola, Denis Furling, Jack Puymirat, Benoit Chabot

    Published in PLoS ONE (2014-01-01)
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  16. 16

    circARHGAP10 as a candidate biomarker and therapeutic target in myotonic dystrophy type 1 by Denisa Baci, Spyros Tastsoglou, Claudia Provenzano, Alessandra Perfetti, Mariapaola Izzo, Mario Lisanti, Svetlana Frolova, Christine Voellenkle, Anna Sofia Tascini, Rosanna Cardani, Beatrice Cardinali, Giovanni Meola, Germana Falcone, Fabio Martelli

    Published in Molecular Therapy: Nucleic Acids (2025-09-01)
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