A very late onset AChR and MuSK double positive myasthenia gravis: a case description and literature review
Pugliese, A., Nicocia, G., Messina, S., Toscano, A., Rodolico, C.
Published in Neuromuscular disorders : NMD (01.02.2023)
Published in Neuromuscular disorders : NMD (01.02.2023)
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MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients
Fiorillo, C, Astrea, G, Savarese, M, Cassandrini, D, Brisca, G, Trucco, F, Pedemonte, M, Trovato, R, Ruggiero, L, Vercelli, L, D'Amico, A, Tasca, G, Pane, M, Fanin, M, Bello, L, Broda, P, Musumeci, O, Rodolico, C, Messina, S, Vita, G L, Sframeli, M, Gibertini, S, Morandi, L, Mora, M, Maggi, L, Petrucci, A, Massa, R, Grandis, M, Toscano, A, Pegoraro, E, Mercuri, E, Bertini, E, Mongini, T, Santoro, L, Nigro, V, Minetti, C, Santorelli, F M, Bruno, C
Published in Orphanet journal of rare diseases (07.07.2016)
Published in Orphanet journal of rare diseases (07.07.2016)
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Value of insoluble PABPN1 accumulation in the diagnosis of oculopharyngeal muscular dystrophy
Galimberti, V., Tironi, R., Lerario, A., Scali, M., Del Bo, R., Rodolico, C., Brizzi, T., Gibertini, S., Maggi, L., Mora, M., Toscano, A., Comi, G. P., Sciacco, M., Moggio, M., Peverelli, L.
Published in European journal of neurology (01.04.2020)
Published in European journal of neurology (01.04.2020)
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Clinical and molecular aspects of 30 patients with late-onset Pompe disease (LOPD): unusual features and response to treatment
Montagnese, Federica, Barca, E., Musumeci, O., Mondello, S., Migliorato, A., Ciranni, A., Rodolico, C., De Filippi, P., Danesino, C., Toscano, A.
Published in Journal of neurology (01.04.2015)
Published in Journal of neurology (01.04.2015)
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Phenotypic clustering of lamin A/C mutations in neuromuscular patients
Benedetti, S, Menditto, I, Degano, M, Rodolico, C, Merlini, L, D'Amico, A, Palmucci, L, Berardinelli, A, Pegoraro, E, Trevisan, C P, Morandi, L, Moroni, I, Galluzzi, G, Bertini, E, Toscano, A, Olivè, M, Bonne, G, Mari, F, Caldara, R, Fazio, R, Mammì, I, Carrera, P, Toniolo, D, Comi, G, Quattrini, A, Ferrari, M, Previtali, S C
Published in Neurology (18.09.2007)
Published in Neurology (18.09.2007)
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Expanding the histopathological spectrum of CFL2‐related myopathies
Fattori, F., Fiorillo, C., Rodolico, C., Tasca, G., Verardo, M., Bellacchio, E., Pizzi, S., Ciolfi, A., Fagiolari, G., Lupica, A., Broda, P., Pedemonte, M., Moggio, M., Bruno, C., Tartaglia, M., Bertini, E., D'Amico, A.
Published in Clinical genetics (01.06.2018)
Published in Clinical genetics (01.06.2018)
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Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy
Broccolini, A, Gidaro, T, Tasca, G, Morosetti, R, Rodolico, C, Ricci, E, Mirabella, M
Published in Neurology (20.07.2010)
Published in Neurology (20.07.2010)
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Long-term follow-up in infantile-onset lambert-eaton myasthenic syndrome
Portaro, S, Parisi, D, Polizzi, A, Ruggieri, M, Andreetta, F, Bernasconi, P, Toscano, A, Rodolico, C
Published in Journal of child neurology (01.09.2014)
Published in Journal of child neurology (01.09.2014)
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T.P.34
Toscano, A, Ferlazzo, E, Romeo, S, Montagnese, F, Aguglia, U, Rodolico, C, Musumeci, O
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Blood film examination for vacuolated and PAS-positive lymphocytes as diagnostic screening test for patients with late onset Pompe disease (LOPD)
Toscano, A, Parisi, D, Montagnese, F, Marino, M, Migliorato, A, Ciranni, A, Rodolico, C, Musumeci, O
Published in Neuromuscular disorders : NMD (01.10.2015)
Published in Neuromuscular disorders : NMD (01.10.2015)
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Intracranial arterial abnormalities in patients with late onset Pompe disease
Toscano, A, Montagnese, F, Granata, F, Rodolico, C, Mondello, S, Cucinotta, M, Ciranni, A, Longo, M, Musumeci, O
Published in Neuromuscular disorders : NMD (01.10.2015)
Published in Neuromuscular disorders : NMD (01.10.2015)
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MicroRNA signatures predict dysregulated vitamin D receptor and calcium pathways status in limb girdle muscle dystrophies (LGMD) 2A/2B
Aguennouz, M., Lo Giudice, C., Licata, N., Rodolico, C., Musumeci, O., Fanin, M., Migliorato, A., Ragusa, M., Macaione, V., Di Giorgio, R. M., Angelini, C., Toscano, A.
Published in Cell biochemistry and function (01.08.2016)
Published in Cell biochemistry and function (01.08.2016)
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Italian recommendations for Lambert–Eaton myasthenic syndrome (LEMS) management
Evoli, A., Liguori, R., Romani, A., Mantegazza, R., Di Muzio, A., Giometto, B., Pegoraro, E., Rodolico, C., Vigliani, M. C.
Published in Neurological sciences (01.04.2014)
Published in Neurological sciences (01.04.2014)
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Central and peripheral autonomic failure in cold-induced sweating syndrome type 1
Di Leo, R, Nolano, M, Boman, H, Pierangeli, G, Provitera, V, Knappskog, P M, Cortelli, P, Vita, G, Rodolico, C
Published in Neurology (26.10.2010)
Published in Neurology (26.10.2010)
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ANT1 is reduced in sporadic inclusion body myositis
Barca, E., Aguennouz, M., Mazzeo, A., Messina, S., Toscano, A., Vita, G. L., Portaro, S., Parisi, D., Rodolico, C.
Published in Neurological sciences (01.02.2013)
Published in Neurological sciences (01.02.2013)
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T.P.16
Montagnese, F, Musumeci, O, Barca, E, Romeo, S, Ciranni, A, Aguennouz, M, Rodolico, C, Toscano, A
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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P.17.10 New ETFDH mutations in a group of Italian patients with Riboflavin-Responsive Multiple Acyl-CoA Dehydrogenase Deficiency (RR-MADD)
Toscano, A, Barca, E, Rodolico, C, Romeo, S, Ciranni, A, Aguennouz, M, Vita, G, Musumeci, O
Published in Neuromuscular disorders : NMD (01.10.2013)
Published in Neuromuscular disorders : NMD (01.10.2013)
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RAGE-NF-κB pathway activation in response to oxidative stress in facioscapulohumeral muscular dystrophy
Macaione, V., Aguennouz, M., Rodolico, C., Mazzeo, A., Patti, A., Cannistraci, E., Colantone, L., Di Giorgio, R. M., De Luca, G., Vita, G.
Published in Acta neurologica Scandinavica (01.02.2007)
Published in Acta neurologica Scandinavica (01.02.2007)
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P1.43 Dual-echo dual flip angle gradient-echo MRI technique for quantification of muscle fat fraction in Duchenne muscular dystrophy: A new valuable outcome measure
Messina, S, Vita, G.L, Rodolico, C, Toscano, A, Gaeta, M, Mileto, A
Published in Neuromuscular disorders : NMD (01.10.2011)
Published in Neuromuscular disorders : NMD (01.10.2011)
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