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Programma - Società italiana di neurologia

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785. LAMBERT–EATON MYASTENIC SYNDROME (LEMS) REVEALING<br />

INTRAVENOUS MULTIPLE UTERINE LEIOMYOMAS: CAUSAL OR<br />

INCIDENTAL<br />

G. GALASSI, E. CANALI, G. GALASSI, V. AGNOLETTO, A. ARIATTI, F. RIVASI (Modena)<br />

786. SOMATIC AND AUTONOMIC SMALL FIBRES NEUROPATHY INDUCED<br />

BY BORTEZOMIB THERAPY: AN IMMUNOFLUORESCENCE STUDY<br />

M.P. GIANNOCCARO, V. DONADIO, C. GOMIS PÈREZ, W. BORSINI, V. DI STASI, R.<br />

LIGUORI (Bologna, Firenze)<br />

787. ABNORMAL VASCULAR SMOOTH MUSCLE CELLS PROLIFERATION<br />

IN SURAL NERVE BIOPSY<br />

M. LUIGETTI, A. CONTE, F. MADIA, A. MODONI, N. MONTANO, A. DEL GRANDE,<br />

P. TONALI, M. SABATELLI (Roma)<br />

788. MULTIFOCAL ACQUIRED DEMYELINATING SENSORY AND MOTOR<br />

NEUROPATHY HERALDING POEMS SYNDROME ASSOCIATED WITH<br />

CASTLEMAN DISEASE<br />

F. LUPIDI, P. DI BELLA, S. RUPOLI, G. GOTERI, F. LOGULLO (Ancona)<br />

789. CO-OCCURRENCE OF AMYOTROPHIC LATERAL SCLEROSIS AND<br />

CHARCOT-MARIE-TOOTH DISEASE TYPE 2A IN A PATIENT WITH A<br />

NOVEL MUTATION IN THE MITOFUSIN-2 GENE<br />

C. MARCHESI, C. CIANO, E. SALSANO, L. NANETTI, M. MILANI, C. GELLERA, F.<br />

TARONI, G. FABRIZI, A. UNCINI, D. PAREYSON (Milano, Verona, Chieti - Pescara)<br />

790. ATYPICAL CASE OF SMA4 MIMICKING A MIOPATHY<br />

D. MARINO, A. MIGNARRI, F. SICURELLI, A. MALANDRINI, C. RICCI, S. BATTISTINI,<br />

A. FEDERICO, M. DOTTI, S. PALMERI (Siena)<br />

791. NOVEL HLA CLASS II ASSOCIATIONS IN MYASTHENIA GRAVIS<br />

R. MASSA, M. ANDREANI, C. TERRACCIANO, G. MARFIA, G. BERNARDI, M. TESTI (Roma)<br />

792. UNUSUAL ANTI-GAD ANTIBODIES - RELATED PHENOTYPE: A CASE REPORT<br />

S. PIAZZA, L. PETRUCCI, E. CALDARAZZO IENCO, R. CALABRESE, M. MANCUSO, G.<br />

SICILIANO (Pisa)<br />

793. RIBOFLAVIN RESPONSIVE TYPE III MULTIPLE ACYL-COA DEFICIENCY<br />

PRESENTING WITH MULTISYSTEM NEUROLOGICAL INVOLVEMENT<br />

AND DRUG-RESISTANT EPILEPSY CAUSED BY FOCAL CORTICAL<br />

DYSPLASIA<br />

G. PICCOLO, I. SARTORI, M. COSSU, C. GALIMBERTI, M. TERZAGHI, A. BERARDINELLI<br />

(Pavia, Milano)<br />

794. ABERRANT SPLICING IN LMNA GENE CAUSED BY A NOVEL MUTATION<br />

ON THE POLYPYRIMIDINE TRACT OF THE INTRON 5<br />

R. PIRAS, G. MARROSU, N. CARBONI, A. MATTEDDU, E. SOLLA, M. MAIOLI, M.<br />

FLORIS, G. COGHE, J. FRAU, G. FENU, L. LOREFICE, M. MARROSU (Cagliari, Pula -<br />

CA)<br />

795. AMYLOIDOGENIC TTR VARIANTS ACTIVATE APOPTOTIC PATHWAYS<br />

BY OXIDATIVE STRESS<br />

L. PRADOTTO, L. VIGNA, G. WALKER, A. MAURO (Piancavallo - VB, Novara, Torino)<br />

796. A CASE OF CMT 1B DUE TO VAL 102/FS NULL MUTATION OF THE MPZ<br />

GENE PRESENTING AS HYPERCKEMIA<br />

R. RENNA, M. LUIGETTI, G. SILVESTRI, E. RICCI, M. SABATELLI (Roma)<br />

797. FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY PRESENTING WITH<br />

MORPHOLOGICAL FEATURES OF INFLAMMATORY MYOPATHY WITH<br />

RIMMED VACUOLES<br />

G. RICCI, V. IACOPETTI, L. VOLPI, F. BERTOLUCCI, D. ORSUCCI, G. ALÌ, L.<br />

POLLINA, R. TUPLER, R. NERI, G. SICILIANO (Pisa, Modena)<br />

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