Programma - Società italiana di neurologia
Programma - Società italiana di neurologia
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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