programma definitivo - Società italiana di neurologia
programma definitivo - Società italiana di neurologia
programma definitivo - Società italiana di neurologia
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
3<br />
N<br />
O<br />
V<br />
E<br />
M<br />
B<br />
R<br />
E<br />
•<br />
A<br />
R<br />
E<br />
A<br />
P<br />
O<br />
S<br />
T<br />
E<br />
R<br />
229. IMATINIB AS A POSSIBLE CAUSE OF MYOPATHY<br />
A. CARNEVALE, E. DI SCIPIO, L. CONTI, G. ACIERNO, M. GARIBALDI, E. PENNISI,<br />
G. ANTONINI (Roma)<br />
230. SERIOUS GAMES AND TECHNOLOGY-ENHANCED LEARNING APPLIED<br />
TO STROKE PREVENTION<br />
T. TASSINARI, G. VERCELLI, L. LAGOMARSINO, A. SUGO, S. BONISSONI, F. CENTANARO,<br />
P. L ANTERI, E. COCO, S. TONINI, M. TRUCCO, M. BANDETTINI DI POGGIO (Pietra<br />
Ligure - SV, Savona)<br />
231. EPIDEMIOLOGY AND POTENTIAL PROGNOSTIC FACTORS IN GUILLAIN<br />
BARRÈ SYNDROME: TEN YEARS’ EXPERIENCE OF POLICLINICO TOR<br />
VERGATA<br />
G. MATALUNI, S. ROSSI, A. MARTINI, C. ROCCHI, M. MANGIARDI, M. RAINONE, G.<br />
MARFIA (Roma)<br />
232. EARLY BRAINSTEM INVOLVEMENT IN MYOTONIC DYSTROPHY TYPE-1<br />
M. TRIMBOLI, M. MORELLI, D. SALVINO, A. CHERUBINI, M. CURCIO, S. NIGRO, M.<br />
R. MAZZA, P. PERROTTA, A. QUATTRONE, F. BONO (Catanzaro)<br />
233. NEW MUTATION IN ND2 GENE ASSOCIATED WITH EXERCISE<br />
INTOLERANCE<br />
C. LAMPERTI, A. POTIC, F. CARRARA, D. DIODATO, F. BLASEVIC, M. MORA, L. MORANDI,<br />
M. ZEVIANI (Milano, Belgrado - SRB, Cambridge - UK)<br />
234. FUNCTIONAL CHARACTERIZATION OF NOVEL CLC-1 MUTATIONS<br />
IDENTIFIED IN MYOTONIA CONGENITA PATIENTS<br />
C. ALTAMURA, S. PORTARO, N. LICATA, C. RODOLICO, O. MUSUMECI, M. DINARDO,<br />
P. IMBRICI, A. TOSCANO, J. DESAPHY, D. CONTE CAMERINO (Bari, Messina)<br />
235. OPA 1 GENE MUTATION IN ITALIAN FAMILY WITH OPTIC ATROPHY,<br />
SENSORI-NEURAL DEAFNESS AND MYOPATHY<br />
O. FARINA, F. CIPULLO, D. FORMICOLA, T. ESPOSITO, G. FRANZESE, G. PANELLA, S.<br />
SAMPAOLO, F. SANTORELLI, G. DI IORIO (Napoli, Pisa)<br />
236. X-LINKED CHARCOT-MARIE-TOOTH TYPE 1 (CMTX1): TRANSIENT<br />
CENTRAL NERVOUS SYSTEM INVOLVEMENT AS INITIAL “STROKE-<br />
LIKE” PRESENTATION OF A NOVEL GJB1 MUTATION<br />
A. SAGNELLI, G. PISCOSQUITO, L. CHIAPPARINI, C. CIANO, M. MILANI, F. TARONI,<br />
D. PAREYSON (Milano)<br />
237. CPEO PHENOTYPE AND HUNTINGTON DISEASE WITH REDUCED<br />
PENETRANCE: DOUBLE TROUBLE OR SINGLE DISEASE<br />
F. RINALDI, E. MARCHINA, A. TODESCHINI, V. VIELMI, S. ROTA, M. COTELLI, A.<br />
PADOVANI, M. FILOSTO (Brescia)<br />
238. NEUROMYOTONIA ASSOCIATED WITH MYASTHENIA GRAVIS AND<br />
THYMOMA<br />
A. DE ROSA, R. RICCIARDI, L. KIFERLE (Pisa)<br />
239. COEXISTENCE OF ANTI-ACHR AND ANTI-MUSK ANTIBODIES IN<br />
PATIENTS AFFECTED BY MYASTHENIA GRAVIS AND THYMOMA<br />
R. RICCIARDI, A. DE ROSA, L. KIFERLE (Pisa)<br />
240. CAMPTOCORMIA AND DROPPED HEAD SYNDROME AS A PRESENTING<br />
SIGN OF MYOFIBRILLAR MYOPATHY<br />
F. NALDI, M. VALENTINO, M. COLUMBARO, P. AVONI, F. BISULLI, F. CATANI, V. CARELLI,<br />
R. LIGUORI (Bologna, Modena)<br />
146
Change language