Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophy von Mendell, Jerry R., Goemans, Nathalie, Lowes, Linda P., Alfano, Lindsay N., Berry, Katherine, Shao, James, Kaye, Edward M., Mercuri, Eugenio

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Galactose‐1‐phosphate uridyltransferase deficiency: A literature review of the putative mechanisms of short and long‐term complications and allelic variants von Viggiano, E., Marabotti, A., Politano, L., Burlina, A.

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Comparison of X-chromosome inactivation in Duchenne muscle/myocardium-manifesting carriers, non-manifesting carriers and related daughters von Viggiano, E, Picillo, E, Cirillo, A, Politano, L

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Functional changes in Duchenne muscular dystrophy von Mazzone, E, Vasco, G, Sormani, M P, Torrente, Y, Berardinelli, A, Messina, S, D'Amico, A, Doglio, L, Politano, L, Cavallaro, F, Frosini, S, Bello, L, Bonfiglio, S, Mercuri, E

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The lack of the Celf2a splicing factor converts a Duchenne genotype into a Becker phenotype von Martone, J., Briganti, F., Legnini, I., Morlando, M., Picillo, E., Sthandier, O., Politano, L., Bozzoni, I.

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Prevalence study of muscle channelopathies in Italy von Maggi, L, Lo Monaco, M, Portaro, S, Meola, G, Desaphy, J, Lucchiari, S, Pagliarani, S, Bernasconi, P, Imbrici, P, Comi, G, Mantegazza, R, Trojano, M, D'Amico, A, Pegoraro, E, Politano, L, Mongini, T, Siciliano, G, Conte Camerino, D, Toscano, A, Sansone, V

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Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases von Sansone, V. A., Panzeri, M., Montanari, M., Apolone, G., Gandossini, S., Rose, M. R., Politano, L., Solimene, C., Siciliano, G., Volpi, L., Angelini, C., Palmieri, A., Toscano, A., Musumeci, O., Mongini, T., Vercelli, L., Massa, R., Panico, M. B., Grandi, M., Meola, G.

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G.P.228 von D’Ambrosio, P, Picillo, E, Petillo, R, Taglia, A, Torella, A, Nigro, V, Politano, L

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Muscle MRI in female carriers of emerinopathy von Carboni, N., Mura, M., Politano, L., Cocco, E., Marrosu, G., Marrosu, M. G.

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Eye involvement in patients with myotonic dystrophy von Vitiello, L, Politano, L, De Bernardo, M, Rosa, N

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Risk of arrhythmia in type I myotonic dystrophy: the role of clinical and genetic variables von Cudia, P, Bernasconi, P, Chiodelli, R, Mangiola, F, Bellocci, F, Russo, A Dello, Angelini, C, Romeo, V, Melacini, P, Politano, L, Palladino, A, Nigro, G, Siciliano, G, Falorni, M, Bongiorni, M G, Falcone, C, Mantegazza, R, Morandi, L

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Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes von Piluso, G, Politano, L, Aurino, S, Fanin, M, Ricci, E, Ventriglia, V M, Belsito, A, Totaro, A, Saccone, V, Topaloglu, H, Nascimbeni, A C, Fulizio, L, Broccolini, A, Canki-Klain, N, Comi, L I, Nigro, G, Angelini, C, Nigro, V

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Implicación ocular en pacientes con distrofia miotónica von Vitiello, L., Politano, L., De Bernardo, M., Rosa, N.

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P.6.4 Salbutamol tolerability and efficacy in adult type III SMA patients: Results of a multicentric, molecular and clinical, double-blind, placebo-controlled study von Morandi, L, Abiusi, E, Pasanisi, M.B, Lomastro, R, Fiori, S, Di Pietro, L, Angelini, C, Sorarù, G, Gaiani, A, Mongini, T, Vercelli, L, Vasco, G, Vita, G, Vita, G.L, Messina, S, Politano, L, Passamano, L, Gregorio, G. Di, Tiziano, F.D

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G.P.223 von Scutifero, M, Taglia, A, D’Ambrosio, P, Petillo, R, Passamano, L, Palladino, A, Nigro, V, Nigro, G, Politano, L

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Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols von Biggar, W.D., Politano, L., Harris, V.A., Passamano, L., Vajsar, J., Alman, B., Palladino, A., Comi, L.I., Nigro, G.

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Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes von Vytopil, M, Benedetti, S, Ricci, E, Galluzzi, G, Dello Russo, A, Merlini, L, Boriani, G, Gallina, M, Morandi, L, Politano, L, Moggio, M, Chiveri, L, Hausmanova-Petrusewicz, I, Ricotti, R, Vohanka, S, Toman, J, Toniolo, D

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Large screening of patients diagnosed as limb girdle muscular dystrophy or congenital myopathy using Motorplex von Savarese, M, Di Fruscio, G, Bruno, C, Torella, A, Giugliano, T, Mora, M, Morandi, L, Siciliano, G, Toscano, A, Garofalo, A, Mongini, T, Angelini, C, Santoro, L, Claes, K, Bertini, E, Santorelli, F, Comi, G, Sacconi, S, Politano, L, Nigro, V

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Molecular diagnosis in LGMD2A: Mutation analysis or protein testing? von Fanin, M., Fulizio, L., Nascimbeni, A.C., Spinazzi, M., Piluso, G., Ventriglia, V.M., Ruzza, G., Siciliano, G., Trevisan, C.P., Politano, L., Nigro, V., Angelini, C.

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Evaluation of cardiac and respiratory involvement in sarcoglycanopathies von Politano, L, Nigro, V, Passamano, L, Petretta, V, Comi, L.I, Papparella, S, Nigro, Ge, Rambaldi, P.F, Raia, P, Pini, A, Mora, M, Giugliano, M.A.M, Esposito, M.G, Nigro, G

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