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5 N O V E M B R E • A R E A P O S T E R 777. SLOWLY PROGRESSIVE DYSARTHRIA: RARE DISEASE ENTITY OR CHAMALEON E.L. SUSANI, L. TREMOLIZZO, C. FERRARESE, I. APPOLLONIO (Monza) 778. AD BIOMARKERS IN SUBJECTIVE COGNITIVE IMPAIRMENT: VERY EARLY PREDICTORS OR SWORD OF DAMOCLES L. VOLPI, C. PAGNI, C. CARLESI, S. CINTOLI, I. FALORNI, C. RADICCHI, I. GHICOPULOS, G. TOGNONI (Pisa) 779. FRONTOTEMPORAL DEMENTIA ASSOCIATED TO PROGRESSIVE SUPRANUCLEAR PALSY: A FURTHER VARIANT OF THE FRONTOTEMPORAL LOBE DEGENERATION S. BALDINELLI, V. CAFAZZO, E. CURSI, K. FABI, F. GIRELLI, P. PETTINARI, L. PROVINCIALI, S. LUZZI (Ancona) 780. CAN CSF BIOMARKERS PROFILE CHANGE INITIAL CLINICAL DIAGNOSIS AND PREDICT DISEASE PROGRESSION C. CARLESI, L. PETROZZI, C. PAGNI, L. VOLPI, A. NOVELLI, I. GHICOPULOS, G. SICILIANO, U. BONUCCELLI, G. TOGNONI (Pisa) 781. COMBINATION OF PHARMACOLOGICAL AND NON-PHARMACOLOGICAL TREATMENT IN MODERATE ALZHEIMER’S DISEASE: COGNITIVE AND PSYCHO-BEHAVIOURAL EFFECTS A. PARENTE, V. MANFREDI, L. SCHIFANO, S. OLIVERI, F. ALLARIA, A. PUGLIESE, A. GIOVAGNOLI (Milano) 782. EPIDEMIOLOGY OF VASCULAR, BEHAVIOURAL AND THYROID DISEASE COMORBILITY IN PATIENTS WITH MENTAL RETARDATION M. PACE, N. CARLINO (Vasto Marina - CH) 783. TELE-HEALTH-CARE IN THE ELDERLY: A SICILIAN MULTIMODAL APPROACH R. DE LUCA, A. BRAMANTI, G. LAMPONI, S. REITANO, A. LEO, R. CALABRÒ, P. BRAMANTI (Messina) 784. TINER: INTEGRATED TREATMENT NEUROMUSCULAR RELAXING EMOTIONAL MOOD DISORDERS ASSOCIATED WITH ALZHEIMER’S DEMENTIA IN MEMANTINE TREATMENT A. LERA (L’Aquila, Giulianova - TE) 785. POSTERIOR CORTICAL ATROPHY: A CASE REPORT M.G. GARGIULO, M. PROTO, G. CAPALDO, M. MELONE (Napoli) 786. DISCRIMINATION OF ALZHEIMER’S DISEASE AND MILD COGNITIVE IMPAIRMENT BASED ON EEG MEASURES L. BONANNO, S. DE SALVO, A. CAIZZONE, A. BRAMANTI, F. MORABITO, P. BRAMANTI (Messina, Reggio Calabria) 787. CORRELATION BETWEEN CREATIVITY AND COGNITIVE FUNCTIONS IN A PATIENT WITH ALZHEIMER DISEASE: A CASE REPORT M. TULLII, P. SUCAPANE (L’Aquila) NEUROGENETICA CLINICA Moderatori F. MARTINELLI BONESCHI (Milano) - E. PARATI (Milano) 788. KIF5A GENE MUTATIONS IN PATIENTS WITH SPASTIC PARAPLEGIA D. DI BELLA, S. CALDARAZZO, E. SARTO, S. BARATTA, K. SAVIO, G. GALASSI, A. ARIATTI, T. MONGINI, A. CHIÒ, S. AMIDEI, D. LAURIA, L. NANETTI, E. SALSANO, D. PAREYSON, C. MARIOTTI, F. TARONI (Milano, Biella, Modena, Torino) 194
789. A NEW CACNA1A GENE MUTATION PRESENTING ALTERNATIVELY WITH SCA6 AND EA2 PHENOTYPES L. PRADOTTO, M. MENCARELLI, A. MILESI, A. DI BLASIO, A. MAURO (Milano, Torino) 790. SCA19/SCA22 MOLECULAR ANALYSIS IN PATIENTS WITH SPINOCEREBELLAR ATAXIA D. DI BELLA, E. SARTO, S. CALDARAZZO, C. CALLEGARINI, F. LOGULLO, C. GELLERA, F. TARONI (Milano, Ravenna, Ancona) 791. MITOFUSIN-2 GENE SEQUENCE VARIATIONS AND GENOTYPE- PHENOTYPE CORRELATIONS G. PISCOSQUITO, I. MORONI, M. MILANI, P. SAVERI, S. BARATTA, F. TARONI, D. PAREYSON (Milano) 792. TYPE B KUFS DUE TO A NOVEL CTSF MUTATION IN A LARGE ITALIAN PEDIGREE C. DAVASSI, F. MORO, M. MESCHINI, R. DI FABIO, L. PESTILLO, M. SERRAO, C. CASALI, A. SIMONATI, F. SANTORELLI, F. PIERELLI (Latina, Pisa, Fon<strong>di</strong> - LT, Verona, Pozzilli - IS) 793. HOMOZYGOSITY FOR P.CYS183SER MUTATION IN NOTCH3 GENE MAY INFLUENCE THE SEVERITY OF CLINICAL PRESENTATION REPORT OF AN ITALIAN FAMILY S. BIANCHI, A. RUFA, C. VINCIGUERRA, G. GALLUS, M. DOTTI, A. FEDERICO (Siena) 794. POLG1 GENE MUTATIONS IN PATIENTS WITH INTELLECTUAL DISABILITY C. SCUDERI, M. LO GIUDICE, E. BORGIONE, F. CASTELLO, M. SAVIO, F. DI BLASI, G. VITELLO, G. BARBARINO, R. PETTINATO, S. MUSUMECI (Troina - EN) 795. DIGENIC MUTATION INHERITANCE OF INTEGRIN ALPHA 7 AND MYOSIN HEAVY CHAIN 7B GENES CAUSES CONGENITAL MYOPATHY WITH LEFT VENTRICULAR NON COMPACT CARDIOMYOPATHY D. FORMICOLA, T. ESPOSITO, F. NAPOLITANO, F. GIANFRANCESCO, G. LIMONGELLI, O. FARINA, D. DIODATO, F. CIPULLO, S. SAMPAOLO, G. DI IORIO (Napoli) 796. PGRN A POSSIBLE MODIFIER GENE IN FTLD NEURODEGENERATIVE DISORDER E. VITALE, A. IULIANO, A. POLVERINO, A. POSTIGLIONE, P. SORRENTINO, G. MILAN, S. PAPPATÀ, G. SORRENTINO (Pozzuoli - NA, Napoli) 797. A PILOT, RANDOMIZED, PLACEBO-CONTROLLED, TRIAL OF LITHIUM IN SPINOCEREBELLAR ATAXIA TYPE 2 F. SACCÀ (Napoli) 798. C19ORF12 MUTATIONS IN NEURODEGENERATION WITH BRAIN IRON ACCUMULATION (NBIA) G. ANNESI, P. TARANTINO, M. GAGLIARDI, G. LESCA, E. BROUSSOLLE, A. GAMBARDELLA, A. QUATTRONE (Mangone - CS, Lione - F, Germaneto - CZ) 799. REVERSIBLE SUBACUTE ENCEPHALOPATHY INDUCED BY THERAPEUTIC DOSES OF VALPROATE IN AN ADULT WOMAN WITH THE NT. 8393 C>T MITOCHONDRIAL DNA MUTATION P. SORRENTINO, C. NESTI, L. RUGGIERO, A. ANTENORA, A. ROCA, M. QUARANTELLI, L. SANTORO, A. FILLA, F. SANTORELLI, G. DE MICHELE (Napoli, Pisa) 800. RELATIONSHIP BETWEEN CLINICAL AND MRI FINDINGS IN PATIENTS WITH SPG4-RELATED SPASTIC PARAPLEGIA M.A. CARLUCCIO, M.L. STROMILLO, M. BATTAGLINI, A. TESSA, F. M. SANTORELLI, N. DE STEFANO, M.T. DOTTI (Siena, Pisa) 801. OPTIC NEUROPATHY AND BILATERAL BRAINSTEM LESIONS ASSOCIATED WITH THE M.4171C>A/MT-ND1 MTDNA MUTATION C. LA MORGIA, L. CAPORALI, F. TONI, S. NASSETTI, D. BRUNETTO, A. PARMEGGIANI, A. TORRONI, V. CARELLI (Bologna, Pavia) 5 N O V E M B R E • A R E A P O S T E R 195
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