Secondary hypokalemic periodic paralysis as a rare clinical presentation of Conn syndrome by Nicoletti, T., Modoni, A., Silvestri, G.

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DJ‐1 modulates mitochondrial response to oxidative stress: clues from a novel diagnosis of PARK7 by Di Nottia, M., Masciullo, M., Verrigni, D., Petrillo, S., Modoni, A., Rizzo, V., Di Giuda, D., Rizza, T., Niceta, M., Torraco, A., Bianchi, M., Santoro, M., Bentivoglio, A.R., Bertini, E., Piemonte, F., Carrozzo, R., Silvestri, G.

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Cognitive impairment in myotonic dystrophy type 1 (DM1): A longitudinal follow-up study by Modoni, A., Silvestri, G., Vita, M. Gabriella, Quaranta, D., Tonali, P. A., Marra, C.

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Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study by Masciullo, M, Iannaccone, E, Bianchi, M.L.E, Santoro, M, Conte, G, Modoni, A, Monforte, M, Tasca, G, Laschena, F, Ricci, E, Silvestri, G

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Do not jump to easy conclusions! Lessons from pitfall in the molecular diagnosis of ARSACS by Masciullo, M., Silvestri, G., Modoni, A., Tessa, A., Bianchi, M.L.E., Santorelli, F.M.

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P10.4 Analysis of ryanodine receptor 1 (RyR1) and voltage-gated Ca2+ channel (VGCC) α1s subunit (Cav 1.1) pre-mRNA splicing and correlation with intracellular calcium signals in my... by Santoro, M, Piacentini, R, Masciullo, M, Grassi, C, Modoni, A, Ricci, E, Silvestri, G

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A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia by Luigetti, M, Modoni, A, Renna, R, Silvestri, G, Ricci, E, Montano, N, Tasca, G, Papacci, M, Monforte, M, Conte, A, Pomponi, M.G, Sabatelli, M

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A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy by Tessa, A., Silvestri, G., de Leva, M. F., Modoni, A., Denora, P. S., Masciullo, M., Dotti, M. T., Casali, C., Melone, M. A. B., Federico, A., Filla, A., Santorelli, F. M.

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Neuropsychiatric lupus erythematosus by Vadacca, M, Buzzulini, F, Rigon, A, Coppolino, G, Palma Modoni, A, Massa, R, Afeltra, A

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G.P.100 Biophysical characterization of hClC-1 chloride channel mutations associated with myotonia congenita by Desaphy, J.F, Gramegna, G, Dinardo, M.M, Modoni, A, Lo Monaco, M, Conte Camerino, D

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P10.5 New mutations in muscle voltage-gated sodium channel and their biophysical properties by Modoni, A, Pagliarani, S, Silvestri, G, D'Amico, A, Redaelli, E, Wanke, E, Comi, G.P, Lo Monaco, M

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A novel mutation in the SACS gene associated with a complicated form of spastic ataxia by Masciullo, M., Modoni, A., Fattori, F., Santoro, M., Denora, P. S., Tonali, P., Santorelli, F. M., Silvestri, G.

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Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression by Pescatori, Mario, Broccolini, Aldobrando, Minetti, Carlo, Bertini, Enrico, Bruno, Claudio, D'amico, Adele, Bernardini, Camilla, Mirabella, Massimiliano, Silvestri, Gabriella, Giglio, Vincenzo, Modoni, Anna, Pedemonte, Marina, Tasca, Giorgio, Galluzzi, Giuliana, Mercuri, Eugenio, Tonali, Pietro A, Ricci, Enzo

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Promoting healthy teenage behaviour across three European countries through the use of a novel smartphone technology platform, PEGASO fit for future: study protocol of a quasi-expe... by Puigdomenech, Elisa, Martin, Anne, Lang, Alexandra, Adorni, Fulvio, Gomez, Santiago Felipe, McKinstry, Brian, Prinelli, Federica, Condon, Laura, Rashid, Rajeeb, Caon, Maurizio, Atkinson, Sarah, Lafortuna, Claudio L, Ciociola, Valentina, Hanley, Janet, McCloughan, Lucy, Castell, Conxa, Espallargues, Mireia

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Cognitive impairment in myotonic dystrophy type 1 (DM1) by Modoni, A, Silvestri, G, Vita, MGabriella, Quaranta, D, Tonali, P A, Marra, C

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Alternative splicing alterations of Ca2+ handling genes are associated with Ca2+ signal dysregulation in myotonic dystrophy type 1 (DM1) and type 2 (DM2) myotubes by Santoro, Massimo, Piacentini, Roberto, Masciullo, Marcella, Bianchi, Maria Laura Ester, Modoni, Anna, Podda, Maria Vittoria, Ricci, Enzo, Silvestri, Gabriella, Grassi, Claudio

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Multiple Skeletal Muscle Metastases from Colon Carcinoma Preceded by Paraneoplastic Dermatomyositis by Landriscina, Matteo, Gerardi, Assunta Maria Teresa, Fersini, Alberto, Modoni, Sergio, Stoppino, Luca Pio, Macarini, Luca, Sanguedolce, Francesca, Bufo, Pantaleo, Neri, Vincenzo

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526 POSTER Acute oxaliplatin neurotoxicity may be related to SK3 polyglutamine tract polymorphism: a translational study by Spada, D, Basso, M, Modoni, A, Inno, A, Cassano, A, Pozzo, C, Schinzari, G, Bagal´, C, Tonali, P.A, Barone, C

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P10.4 Analysis of ryanodine receptor 1 (RyR1) and voltage-gated Ca 2+ channel (VGCC) α1s subunit (Ca v1.1) pre-mRNA splicing and correlation with intracellular calcium signals in m... by Santoro, M., Piacentini, R., Masciullo, M., Grassi, C., Modoni, A., Ricci, E., Silvestri, G.

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A case of CMT 1 B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia by LUIGETTI, M, MODONI, A, POMPONI, M. G, SABATELLI, M, RENNA, R, SILVESTRI, G, RICCI, E, MONTANO, N, TASCA, G, PAPACCI, M, MONFORTE, M, CONTE, A

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