| Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome) M Tristani-Firouzi, JL Jensen, MR Donaldson, V Sansone, G Meola, ... The Journal of clinical investigation 110 (3), 381-388, 2002 | 672 | 2002 |
| Myotonic dystrophies: an update on clinical aspects, genetic, pathology, and molecular pathomechanisms G Meola, R Cardani Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1852 (4), 594-606, 2015 | 370 | 2015 |
| In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria A Chomyn, G Meola, N Bresolin, ST Lai, G Scarlato, G Attardi Molecular and cellular biology 11 (4), 2236-2244, 1991 | 357 | 1991 |
| Common micro‐RNA signature in skeletal muscle damage and regeneration induced by Duchenne muscular dystrophy and acute ischemia S Greco, M De Simone, C Colussi, G Zaccagnini, P Fasanaro, M Pescatori, ... The FASEB Journal 23 (10), 3335-3346, 2009 | 301 | 2009 |
| Cerebral involvement in myotonic dystrophies G Meola, V Sansone Muscle & Nerve: Official Journal of the American Association of …, 2007 | 288 | 2007 |
| Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2) G Meola, V Sansone, D Perani, S Scarone, S Cappa, C Dragoni, ... Neuromuscular Disorders 13 (10), 813-821, 2003 | 279 | 2003 |
| Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis E Matthews, R Labrum, MG Sweeney, R Sud, A Haworth, PF Chinnery, ... Neurology 72 (18), 1544-1547, 2009 | 228 | 2009 |
| Andersen's syndrome: a distinct periodic paralysis V Sansone, RC Griggs, G Meola, LJ Ptacek, R Barohn, S Iannaccone, ... Annals of Neurology: Official Journal of the American Neurological …, 1997 | 228 | 1997 |
| Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2 A Vihola, G Bassez, G Meola, S Zhang, H Haapasalo, A Paetau, ... Neurology 60 (11), 1854-1857, 2003 | 205 | 2003 |
| Mexiletine for symptoms and signs of myotonia in nondystrophic myotonia: a randomized controlled trial JM Statland, BN Bundy, Y Wang, DR Rayan, JR Trivedi, VA Sansone, ... Jama 308 (13), 1357-1365, 2012 | 192 | 2012 |
| Second asymptomatic carotid surgery trial (ACST-2): a randomised comparison of carotid artery stenting versus carotid endarterectomy A Halliday, R Bulbulia, LH Bonati, J Chester, A Cradduck-Bamford, R Peto, ... The Lancet 398 (10305), 1065-1073, 2021 | 180 | 2021 |
| Sodium channel mutations in acetazolamide‐responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis LJ Ptacek, R Tawil, RC Griggs, G Meola, P McManis, RJ Barohn, ... Neurology 44 (8), 1500-1500, 1994 | 178 | 1994 |
| Consensus-based care recommendations for adults with myotonic dystrophy type 1 T Ashizawa, C Gagnon, WJ Groh, L Gutmann, NE Johnson, G Meola, ... Neurology: Clinical Practice 8 (6), 507-520, 2018 | 164 | 2018 |
| Confirmation of the type 2 myotonic dystrophy (CCTG) n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins … LL Bachinski, B Udd, G Meola, V Sansone, G Bassez, B Eymard, ... The American Journal of Human Genetics 73 (4), 835-848, 2003 | 161 | 2003 |
| Reduced cerebral blood flow and impaired visual–spatial function in proximal myotonic myopathy G Meola, V Sansone, D Perani, A Colleluori, S Cappa, M Cotelli, F Fazio, ... Neurology 53 (5), 1042-1042, 1999 | 153 | 1999 |
| Dysregulation and cellular mislocalization of specific miRNAs in myotonic dystrophy type 1 R Perbellini, S Greco, G Sarra-Ferraris, R Cardani, MC Capogrossi, ... Neuromuscular Disorders 21 (2), 81-88, 2011 | 144 | 2011 |
| Clinical variability in Becker muscular dystrophy Genetic, biochemical and immunohistochemical correlates GP Comi, A Prelle, N Bresolin, M Moggio, A Bardoni, A Gallanti, G Vita, ... Brain 117 (1), 1-14, 1994 | 141 | 1994 |
| GSK3β mediates muscle pathology in myotonic dystrophy K Jones, C Wei, P Iakova, E Bugiardini, C Schneider-Gold, G Meola, ... The Journal of clinical investigation 122 (12), 4461-4472, 2012 | 136 | 2012 |
| 140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management B Udd, G Meola, R Krahe, C Thornton, LPW Ranum, G Bassez, W Kress, ... Neuromuscular Disorders 16 (6), 403-413, 2006 | 130 | 2006 |
| Increased apoptosis, Huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjects A Ciammola, J Sassone, L Alberti, G Meola, E Mancinelli, MA Russo, ... Cell Death & Differentiation 13 (12), 2068-2078, 2006 | 122 | 2006 |
