MEOLA, GIOVANNI
MEOLA, GIOVANNI
Dipartimento di Scienze Biomediche per la Salute
Myotonic dystrophies: an update on clinical features, molecular mechanisms, management, and gene therapy
2025 M. Rimoldi, S. Lucchiari, S. Pagliarani, G. Meola, G.P. Comi, E. Abati
circARHGAP10 as a candidate biomarker and therapeutic target in myotonic dystrophy type 1
2025 D. Baci, S. Tastsoglou, C. Provenzano, A. Perfetti, M. Izzo, M. Lisanti, S. Frolova, C. Voellenkle, A.S. Tascini, R. Cardani, B. Cardinali, G. Meola, G. Falcone, F. Martelli
Case report: Multiple approach analysis in a case of clinically assessed myotonia congenita
2024 S. Lucchiari, F. Fortunato, G. Meola, A. Mignarri, S. Pagliarani, S. Corti, G.P. Comi, D. Ronchi
Cardiac risk and myocardial fibrosis assessment with cardiac magnetic resonance in patients with myotonic dystrophy
2024 E. Abati, C. Alberti, V. Tambè, A. Esseridou, G.P. Comi, S. Corti, G. Meola, F. Secchi
Case report: Dihydropyridine receptor (CACNA1S) congenital myopathy, a novel phenotype with early onset periodic paralysis
2024 S.K. Aburahma, L.A. Rousan, M. Shboul, F. Biella, S. Lucchiari, G.P. Comi, G. Meola, S. Pagliarani
Case report: Sodium and chloride muscle channelopathy coexistence: A complicated phenotype and a challenging diagnosis
2022 S. Pagliarani, G. Meola, M. Filareti, G.P. Comi, S. Lucchiari
Co-occurrence of DMPK expansion and CLCN1 mutation in a patient with myotonia
2021 S. Locci, R. Cardani, P. Brunori, S. Lucchiari, G.P. Comi, A. Federico, N. De Stefano, G. Meola, A. Mignarri
Rare Disease : Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1
2020 M. Ali, C.B. Monti, L. Melazzini, R. Cardani, B. Fossati, M. Cavalli, K. Chow, F. Secchi, G. Meola, F. Sardanelli
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4
2020 S. Pagliarani, S. Lucchiari, M. Scarlato, E. Redaelli, A. Modoni, F. Magri, B. Fossati, S.C. Previtali, V.A. Sansone, M. Lecchi, M. Lo Monaco, G. Meola, G.P. Comi
Fragility fractures and bone mineral density in male patients affected by type 1 and type 2 myotonic dystrophy
2020 E. Passeri, V. Sansone, M. Sconfienza, C. Messina, G. Meola, S. Corbetta
Guidelines on clinical presentation and management of nondystrophic myotonias
2020 B.C. Stunnenberg, S. Lo Russo, W. David Arnold, R.J. Barohn, S.C. Cannon, B. Fontaine, R.C. Griggs, M.G. Hanna, E. Matthews, G. Meola, V.A. Sansone, J.R. Trivedi, B.G.M. van Engelen, S. Vicart, J.M. Statland
Report of the third outcome measures in myotonic dystrophy type 1 (OMMYD-3) international workshop Paris, France, June 8, 2015
2018 C. Gagnon, C. Heatwole, L. Hébert, J. Hogrel, L. Laberge, M. Leone, G. Meola, L. Richer, V. Sansone, M. Kierkegaard
Consensus-based care recommendations for adults with myotonic dystrophy type 1.
2018 A.T. 3., C. Gagnon, W. Groh, L. Gutmann, N. Johnson, G. Meola, R.3. Moxley, S. Pandya, M. Rogers, E. Simpson, N. Angeard, G. Bassez, K. Berggren, D. Bhakta, M. Bozzali, A. Broderick, J. Byrne, C. Campbell, E. Cup, J. Day, E. De Mattia, D. Duboc, T. Duong, K. Eichinger, A. Ekstrom, B. van Engelen, B. Esparis, B. Eymard, M. Ferschl, S. Gadalla, B. Gallais, T. Goodglick, C. Heatwole, J. Hilbert, V. Holland, M. Kierkegaard, W. Koopman, K. Lane, D. Maas, A. Mankodi, K. Mathews, D. Monckton, D. Moser, S. Nazarian, L. Nguyen, P. Nopoulos, R. Petty, J. Phetteplace, J. Puymirat, S. Raman, L. Richer, E. Roma, J. Sampson, V. Sansone, B. Schoser, L. Sterling, J. Statland, S. Subramony, C. Tian, C. Trujillo, G. Tomaselli, C. Turner, S. Venance, A. Verma, M. White, S. Winblad
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel
2018 C. Altamura, S. Lucchiari, D. Sahbani, G. Ulzi, G.P. Comi, P. D'Ambrosio, R. Petillo, L. Politano, L. Vercelli, T. Mongini, M.T. Dotti, R. Cardani, G. Meola, M. Lo Monaco, E. Matthews, M.G. Hanna, M.R. Carratù, D. Conte, P. Imbrici, J. Desaphy
Neuropsychological and psychological functioning aspects in myotonic dystrophy type 1 patients in Italy
2018 E. Callus, E.G. Bertoldo, M. Beretta, S. Boveri, R. Cardani, B. Fossati, E. Brigonzi, G. Meola
The role of clinical and neuroimaging features in the diagnosis of CADASIL
2018 A. Bersano, G. Bedini, H.S. Markus, P. Vitali, E. Colli-Tibaldi, F. Taroni, C. Gellera, S. Baratta, L. Mosca, P. Carrera, M. Ferrari, C. Cereda, G. Grieco, S. Lanfranconi, F. Mazucchelli, D. Zarcone, M.L. De Lodovici, G. Bono, G.B. Boncoraglio, E.A. Parati, M.V. Calloni, P. Perrone, B.M. Bordo, C. Motto, E. Agostoni, A. Pezzini, A. Padovani, G. Micieli, A. Cavallini, G. Molini, F. Sasanelli, M. Sessa, G. Comi, N. Checcarelli, M. Carmerlingo, M. Corato, S. Marcheselli, L. Fusi, G. Grampa, D. Uccellini, S. Beretta, C. Ferrarese, B. Incorvaia, C.S. Tadeo, L. Adobbati, V. Silani, G. Faragò, N. Trobia, C. Grond-Ginsbach, L. Candelise, F. Mazzucchelli, M. Guidotti, M. Riva, S. Iurlaro, B.B. Maria, M. Braga, G. Meola, M. Carpo, M. Camerlingo, G. Borutti, M. Delodovici, E.P. Verrengia, L. Tancredi, A. Terruzzi, M. Magoni, E. Del Zotto, P. Bassi, P. Lattuada, E. Ballabio, P. Gambaro, A. Bersano, S. Lanfranconi, B. Corrà, I. Canavero, E. Arbustini, M. Grasso, G.P. Comi, S. Corti, D. Ronchi, G. Merlini, L. Obici, M.T. Bassi, F. Tagliavini, C.G. Ginsbach
Slowly progressing varicella zoster brainstem encephalitis complicating Ramsay Hunt syndrome in an immunocompetent patient : case report and review of the literature
2017 V.A.G. Ricigliano, L. Saraceno, M. Cavalli, M. Rodegher, G. Meola
Myotonic dystrophies : state of the art of new therapeutic developments for the CNS
2017 G. Gourdon, G. Meola
Posterior reversible encephalopathy syndrome after long-term treatment with low-dose sunitinib : a case report
2017 L. Saraceno, V.A..G. Ricigliano, M. Cavalli, G. Meola
Myotonic dystrophy type 2 and modifier genes : an update on clinical and pathomolecular aspects
2017 G. Meola, R. Cardani