23 N O V E M B R E • A R E A P O S T E R 432. PRELIMINARY PREDICTION OF NON-SYNONYMOUS SINGLE NUCLEOTIDE POLYMORPHISMS IN HUMAN NOTCH GENE BY COMPUTATIONAL METHODS C. D'ERAMO, S. BIANCHI, F. PESCINI, L. PANTONI, D. INZITARI, E. ZICARI, G. SERNI, A. FEDERICO, M. DOTTI (Siena, Firenze) 433. GENOMIC BIOMARKERS OF EARLY PARKINSON’S DISEASE AND WEB- BASED APPLICATION FOR DATA COLLECTING A. GORIAN, L. FERIGO, T. CATTARUZZA, R. CALLIGARIS, M. BANICA, L. ANTONUTTI, S. GUSTINCICH, G. PIZZOLATO (Trieste, Basovizza - TS) 434. CERULOPLASMIN GENE VARIATIONS AND PARKINSON’S DISEASE: AN ASSOCIATION STUDY IN SOUTHERN ITALIAN POPULATION F. E. ROCCA, G. ANNESI, V. GRECO, E. DE MARCO, F. ANNESI, G. PROVENZANO, D. CIVITELLI, P. TARANTINO, V. SCORNAIENCHI, M. SALSONE, G. NICOLETTI, M. MORELLI, F. NOVELLINO, A. QUATTRONE (Piano Lago <strong>di</strong> Mangone - CS, Catanzaro, Messina) 435. MULTIPLEX LIGATION-DEPENDENT PROBE AMPLIFICATION (MLPA) ASSAY IN PARK2 GENE ASSOCIATED WITH EARLY ONSET PARKINSONISM G. GRIECO, A. DAVIN, C. PACCHETTI, I. RICCA, F. BLANDINI, S. CRISTINA, R. ZANGAGLIA, C. CEREDA (Pavia) 436. A COMPREHENSIVE MUTATION ANALYSIS OF PINK GENE IN SOUTH ITALY PATIENTS WITH EARLY AND LATE ONSET PARKINSONISM V. SCORNAIENCHI, G. ANNESI, A. UNCINI, E. DE MARCO, D. CIVITELLI, F. ANNESI, P. TARANTINO, F. ROCCA, V. GRECO, G. PROVENZANO, G. NICOLETTI, G. ARABIA, L. GIOFFRÈ, S. PAGLIONICO, A. QUATTRONE (Piano Lago <strong>di</strong> Mangone - CS, Chieti, Messina, Catanzaro) 437. CLINICAL AND GENETIC CHARACTERISTICS OF LATE ONSET HUNTINGTON DISEASE G. CISLAGHI, L. ROMANO, E. CAPILUPPI, M. SUARDELLI, P. BERTORA, C. LOVATI, C. MARIANI (Milano) 438. MUTATIONAL ANALYSIS OF FLG GENE IN ITALIAN PATIENTS AFFECTED BY ATOPIC DERMATITIS V. FOTI CUZZOLA, R. CASCELLA, C. SINIBALDI, C. PECONI, N. PAOLILLO, E. GALLI, E. GIARDINA, P. BRAMANTI , G. NOVELLI (Messina, Roma, Urbino, Little Rock -USA) 439. CONCURRENCE OF SOD1 AND ANG MUTATIONS IN AN ITALIAN ALS FAMILY C. COLOMBRITA, C. GELLERA, N. TICOZZI, A. RATTI, B. CASTELLOTTI, C. BRAGATO, F. TARONI, V. SILANI (Milano) 440. TARDBP GENE ANALYSIS IN ALS PATIENTS G. SORARÙ, V. ORSETTI, A. PALMIERI, C. D'ASCENZO, E. BURATTI, M. MOSTACCIUOLO, M. VOLPE, G. QUERIN, E. PEGORARO, C. ANGELINI (Padova, Trieste) 441. AUTOSOMAL DOMINANT DISTAL MOTOR NEUROPATHY: AN ITALIAN FAMILY NOT LINKED TO KNOWN LOCI M. MUGLIA, L. CITRIGNO, M. PENNISI, A. PATITUCCI, R. BARONE, M. MAGARIELLO, A. GABRIELE, G. PENNISI, R. MAZZEI, F. CONFORTI, C. UNGARO, A. GAMBARDELLA, A. QUATTRONE, M. ZAPPIA (Piano Lago <strong>di</strong> Mangone - CS, Messina, Catania, Catanzaro) 442. CHARCOT-MARIE-TOOTH DISEASE: A NEW TRUNCATING MUTATION IN MPZ GENE S. PIAZZA, G. RICCI, F. BALDINOTTI, A. FOGLI, E. MOLESTI, M. CONIDI, A. MICHELACCI, L. MIGLIORE, P. SIMI, G. SICILIANO (Pisa) 176
443. PAROXYSMAL NON-KINESIGENIC DYSKINESIA IS CAUSED BY MUTATIONS OF THE MR- MITOCHONDRIAL TARGETING SEQUENCE M. ZEVIANI, D. GHEZZI, C. VISCOMI, A. FERLINI, F. GUALANDI, P. MEREGHETTI, D. DE GRANDIS (Milano, Ferrara, Rovigo) 444. ASSOCIATION STUDY OF CDKN2A POLYMORPHISMS IN ITALIAN ALZHEIMER’S DISEASE I. PIACERI, S. BAGNOLI, A. TEDDE, B. NACMIAS, S. MARINI, E. CELLINI, S. PIACENTINI, L. BRACCO, S. SORBI (Firenze) 445. PROGRANULIN GENETIC VARIATIONS IN FTD ITALIAN PATIENTS S. BAGNOLI, B. NACMIAS, A. TEDDE, I. PIACERI, E. CELLINI, G. CIPRIANI, P. NICHELLI, L. BRACCO, S. SORBI (Firenze, Modena) 446. SCREENING FOR PRICKE MUTATIONS IN ITALIAN PATIENTS WITH AUTOSOMAL RECESSIVE PROGRESSIVE MYOCLONUS EPILEPSY-ATAXIA SYNDROME C. CRISCUOLO, P. SORRENTINO, R. CARBONE, A. MARSILI, A. GUACCI, G. DE MICHELE, A. FILLA (Napoli) 447. A POSSIBLE FOUNDER MUTATION AS THE CAUSE OF ADOA IN THE PROVINCE OF SYRACUSE, SICILY G.N. GALLUS, E. CARDAIOLI, A. RUFA, P. DA POZZO, M. COLLURA, A. FEDERICO (Siena, Siracusa) 448. PROGRESSIVE MUSCLE WEAKNESS ASSOCIATED WITH A NOVEL MUTATION IN THE MITOCHONDRIAL TRNASER(AGY) GENE E. CARDAIOLI, P. DA POZZO, E. MALFATTI, G. N. GALLUS, M. A. CARLUCCIO, A. RUFA, N. VOLPI, M. T. DOTTI, A. FEDERICO (Siena) 177 23 N O V E M B R E • A R E A P O S T E R