MEOLA, GIOVANNI
MEOLA, GIOVANNI
Dipartimento di Scienze Biomediche per la Salute
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: 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
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
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
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
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
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
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
Myotonic dystrophies : state of the art of new therapeutic developments for the CNS
2017 G. Gourdon, G. Meola
Clinical Reasoning : a 35-year-old woman with hyperstartling, stiffness, and accidental falls : a startling diagnosis
2017 S.P. Russo, B. Fossati, M. Toffetti, J. Lanzone, R. Cardani, G. Meola
Biomolecular diagnosis of myotonic dystrophy type 2 : a challenging approach
2017 G. Meola, F. Biasini, R. Valaperta, E. Costa, R. Cardani
Receptor and post-receptor abnormalities contribute to insulin resistance in myotonic dystrophy type 1 and type 2 skeletal muscle
2017 L.V. Renna, F. Bose', S. Iachettini, B. Fossati, L. Saraceno, V. Milani, R. Colombo, G. Meola, R. Cardani
Circulating irisn is reduced in male patients with type 1 and type 2 Myotonic Dystrophies
2017 E. Dozio, E. Passeri, R. Cardani, S. Benedini, C. Aresta, R. Valaperta, M. Corsi Romanelli, G. Meola, V. Sansone, S. Corbetta
Myotonic dystrophy type 2 and modifier genes : an update on clinical and pathomolecular aspects
2017 G. Meola, R. Cardani