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3 N O V E M B R E • A R E A P O S T E R 229. IMATINIB AS A POSSIBLE CAUSE OF MYOPATHY A. CARNEVALE, E. DI SCIPIO, L. CONTI, G. ACIERNO, M. GARIBALDI, E. PENNISI, G. ANTONINI (Roma) 230. SERIOUS GAMES AND TECHNOLOGY-ENHANCED LEARNING APPLIED TO STROKE PREVENTION T. TASSINARI, G. VERCELLI, L. LAGOMARSINO, A. SUGO, S. BONISSONI, F. CENTANARO, P. L ANTERI, E. COCO, S. TONINI, M. TRUCCO, M. BANDETTINI DI POGGIO (Pietra Ligure - SV, Savona) 231. EPIDEMIOLOGY AND POTENTIAL PROGNOSTIC FACTORS IN GUILLAIN BARRÈ SYNDROME: TEN YEARS’ EXPERIENCE OF POLICLINICO TOR VERGATA G. MATALUNI, S. ROSSI, A. MARTINI, C. ROCCHI, M. MANGIARDI, M. RAINONE, G. MARFIA (Roma) 232. EARLY BRAINSTEM INVOLVEMENT IN MYOTONIC DYSTROPHY TYPE-1 M. TRIMBOLI, M. MORELLI, D. SALVINO, A. CHERUBINI, M. CURCIO, S. NIGRO, M. R. MAZZA, P. PERROTTA, A. QUATTRONE, F. BONO (Catanzaro) 233. NEW MUTATION IN ND2 GENE ASSOCIATED WITH EXERCISE INTOLERANCE C. LAMPERTI, A. POTIC, F. CARRARA, D. DIODATO, F. BLASEVIC, M. MORA, L. MORANDI, M. ZEVIANI (Milano, Belgrado - SRB, Cambridge - UK) 234. FUNCTIONAL CHARACTERIZATION OF NOVEL CLC-1 MUTATIONS IDENTIFIED IN MYOTONIA CONGENITA PATIENTS C. ALTAMURA, S. PORTARO, N. LICATA, C. RODOLICO, O. MUSUMECI, M. DINARDO, P. IMBRICI, A. TOSCANO, J. DESAPHY, D. CONTE CAMERINO (Bari, Messina) 235. OPA 1 GENE MUTATION IN ITALIAN FAMILY WITH OPTIC ATROPHY, SENSORI-NEURAL DEAFNESS AND MYOPATHY O. FARINA, F. CIPULLO, D. FORMICOLA, T. ESPOSITO, G. FRANZESE, G. PANELLA, S. SAMPAOLO, F. SANTORELLI, G. DI IORIO (Napoli, Pisa) 236. X-LINKED CHARCOT-MARIE-TOOTH TYPE 1 (CMTX1): TRANSIENT CENTRAL NERVOUS SYSTEM INVOLVEMENT AS INITIAL “STROKE- LIKE” PRESENTATION OF A NOVEL GJB1 MUTATION A. SAGNELLI, G. PISCOSQUITO, L. CHIAPPARINI, C. CIANO, M. MILANI, F. TARONI, D. PAREYSON (Milano) 237. CPEO PHENOTYPE AND HUNTINGTON DISEASE WITH REDUCED PENETRANCE: DOUBLE TROUBLE OR SINGLE DISEASE F. RINALDI, E. MARCHINA, A. TODESCHINI, V. VIELMI, S. ROTA, M. COTELLI, A. PADOVANI, M. FILOSTO (Brescia) 238. NEUROMYOTONIA ASSOCIATED WITH MYASTHENIA GRAVIS AND THYMOMA A. DE ROSA, R. RICCIARDI, L. KIFERLE (Pisa) 239. COEXISTENCE OF ANTI-ACHR AND ANTI-MUSK ANTIBODIES IN PATIENTS AFFECTED BY MYASTHENIA GRAVIS AND THYMOMA R. RICCIARDI, A. DE ROSA, L. KIFERLE (Pisa) 240. CAMPTOCORMIA AND DROPPED HEAD SYNDROME AS A PRESENTING SIGN OF MYOFIBRILLAR MYOPATHY F. NALDI, M. VALENTINO, M. COLUMBARO, P. AVONI, F. BISULLI, F. CATANI, V. CARELLI, R. LIGUORI (Bologna, Modena) 146
241. D4Z4 REDUCED ALLELE IN MYOPATHIC SUBJECTS WITH NO FSHD PHENOTYPE: WHY INCONSISTENCY BETWEEN MOLECULAR AND CLINICAL DATA SHOULD PROMPT US TO FURTHER INVESTIGATIONS J. DAOLIO, A. NIKOLIC, G. RICCI, M. GOVI, F. MELE, S. CARRA, M. FILOSTO, L. VERCELLI, G. ANTONINI, A. BERARDINELLI, T. MONGINI, M. SERVIDA, L. RUGGIERO, C. ANGELINI, M. CAO, G. D’ANGELO, A. DI MUZIO, M. MOGGIO, L. MORANDI, E. RICCI, C. RODOLICO, L. SANTORO, G. SICILIANO, G. TOMELLERI, R. TUPLER (Modena, Pisa, Brescia, Torino, Roma, Pavia, Milano, Napoli, Padova, Bosisio Parini - LC, Chieti, Messina, Verona) 242. DUAL ACTIVATION AND SUPPRESSION OF ERK1/2 IN INFLAMMATORY MYOPATHIES AND SPORADIC INCLUSION BODY MYOSITIS F. GIROLAMO, A. LIA, A. AMATI, T. DRAGONE, C. COPPOLA, V. LAVOLPE, S. ZOCCOLELLA, F. LAPENNA, A. TOSCANO, L. SERLENGA, M. TROJANO (Bari, Messina, Andria - BAT) 243. RESTLESS LEG SYNDROME IN DIFFERENT TYPES OF DEMYELINATING NEUROPATHIES: A SINGLE-CENTRE EXPERIENCE M. LUIGETTI, A. DEL GRANDE, A. CONTE, E. TESTANI, G. BISOGNI, A. LOSURDO, A. ROMANO, G. DELLA MARCA, M. SABATELLI (Roma) 244. C.1277 G>A MUTATION IN TWINKLE GENE IN A PEO PLUS SYNDROME L. TIRELLI, A. MALANDRINI, A. RUBEGNI, A. RUFA, A. PICCOLOMO, E. CARDAIOLI, P. DA POZZO, A. FEDERICO (Siena) 245. BREATHING PATTERN AND CENTRAL VENTILATORY DRIVE IN LATE- ONSET POMPE DISEASE (LOPD) F. MONTAGNESE, O. MUSUMECI, P. RUGGERI, E. BARCA, G. GIRBINO, A. TOSCANO (Messina) 246. INCIDENTAL ELECTRICAL MYOTONIA (“LATENT MYOTONIA”) IN CHLORIDE CHANNELOPATHY F. LUPIDI, C. PEROZZI, P. DI BELLA, L. PROVINCIALI, F. LOGULLO (Ancona) 247. MITOCHONDRIAL ABNORMALITIES IN NECK EXTENSOR MYOPATHY: HISTOLOGICAL AND MOLECULAR STUDIES OF SIX PATIENTS A. RUBEGNI, A. MALANDRINI, L. TIRELLI, M. GEORGANTZINOU, I. TAGLIA, P. DA POZZO, E. CARDAIOLI, A. FEDERICO (Siena) NEUROPSICOLOGIA CLINICA Moderatori S. CAPPA (Milano) - E. CATRICALÀ (Milano) 3 N O V E M B R E • A R E A P O S T E R 248. STRIATAL DOPAMINERGIC DYSFUNCTION CONTRIBUTES TO APRAXIA IN CORTICO-BASAL DEGENERATION: A 123-IOFLUPANE SPET STUDY V. ISELLA, M. MUSARRA, G. GELOSA, F. FERRI, C. MESSA, I. APPOLLONIO (Monza) 249. THE APPLAUSE SIGN IN FRONTO-TEMPORAL LOBAR DE GENERATION: WHY AND WHEN INSIGHTS ON ITS NATURE K. FABI, S. BALDINELLI, V. CAFAZZO, P. PETTINARI, F. GIRELLI, E. CURSI, L. PROVINCIALI, S. LUZZI (Ancona) 250. THE 16 ITEM-PRINTED WORD VERSION OF THE FREE AND CUED SELECTIVE REMINDING TEST (FCSRT): NORMAL VALUES IN AN ITALIAN POPULATION N. GIRTLER, C. BRUZZANITI, F. DE CARLI, A. BRUGNOLO, M. AMORE, L. BOSIA, L. COCITO, L. GHIO, M. PARDINI, E. MAGI, G. MANCARDI, R. RISSOTTO, C. SERRATI, G. COLAZZO, S. CAPPA, F. NOBILI (Genova, Menton - F, Milano) 147
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