A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset von TEDDE, A, FORLEO, P, NACMIAS, B, PICCINI, C, BRACCO, L, PIACENTINI, S, SORBI, S

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Clinical and genetic analysis of hereditary and sporadic ataxia in central Italy von CELLINI, E, FORIEO, P, NACMIAS, B, TEDDE, A, LATORRACA, S, PIACENTINI, S, PARNETTI, L, GALLAI, V, SORBI, S

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Technical limits in transcranial doppler recording : Inadequate acoustic windows von MARINONI, M, GINANNESCHI, A, FORLEO, P, AMADUCCI, L

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Alzheimer's Disease and Apolipoprotein E in Italy von SORBI, S., NACMIAS, B., FORLEO, P., PIACENTINI, S., AMADUCCI, L.

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Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer's disease von NACMIAS, Benedetta, TEDDE, Andrea, SORBI, Sandro, FORLEO, Paolo, PIACENTINI, Silvia, GUARNIERI, Bianca Maria, BARTOLI, Antonella, ORTENZI, Luigi, PETRUZZI, Concetta, SERIO, Antonio, MARCON, Gabriella

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ApoE as a prognostic factor for post-traumatic coma von Sorbi, Sandro, Nacmias, Benedetta, Piacentini, Silvia, Repice, Anna, Latorraca, Stefania, Forleo, Paolo, Amaducci, Luigi

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Nail Psoriasis: Combined Therapy with Systemic Cyclosporin and Topical Calcipotriol von Feliciani, Claudio, Zampetti, Anna, Forleo, Pietro, Cerritelli, Luca, Amerio, Paolo, Proietto, Gianluca, Tulli, Antonio, Amerio, Pierluigi

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Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease von Sorbi, Sandro, Nacmias, Benedetta, Forleo, Paolo, Piacentini, Silvia, Latorraca, Stefania, Amaducci, Luigi

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Psychosis, serotonin receptor polymorphism and Alzheimer's disease von Nacmias, B., Tedde, A., Forleo, P., Piacentini, S., Latorraca, S., Guarnieri, B.M., Ortenzi, L., Bartoli, A., Petruzzi, C., Serio, A., Sorbi, S.

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P160 An unusual case of tinea capitis von Rotoli, V., Forleo, P., Cerritelli, L., Andreassi, M., Masci, S., Amerio, P.

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ApoE allele frequencies in Italian sporadic and familial Alzheimer's disease von Sorbi, Sandro, Nacmias, Benedetta, Forleo, Paolo, Latorraca, Stefania, Gobbini, Ida, Bracco, Laura, Piacentini, Silvia, Amaducci, Luigi

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Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia von Cellini, Elena, Forleo, Paolo, Nacmias, Benedetta, Tedde, Andrea, Bagnoli, Silvia, Piacentini, Silvia, Sorbi, Sandro

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Genetic risk factors in familial Alzheimer's disease von Sorbi, Sandro, Forleo, Paolo, Tedde, Andrea, Cellini, Elena, Ciantelli, Monica, Bagnoli, Silvia, Nacmias, Benedetta

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Double-blind, crossover, placebo-controlled clinical trial with L-acetylcarnitine in patients with degenerative cerebellar ataxia von SORBI, S, FORLEO, P, FANI, C, PIACENTINI, S

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Missense mutation of S182 gene in Italian families with early-onset Alzheimer's disease von Sorbi, S, Nacmias, B, Forleo, P, Piacentini, S, Sherrington, R, Rogaev, E, St George Hyslop, P, Amaducci, L

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Absence of APP717 mutation in Italian FAD families von Sorbi, S., Tesco, G., Nacmias, B., Mortilla, M., Forleo, P., Latorraca, S., Piersanti, P., Piacentini, S., Amaducci, L.

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alpha 2-Macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease von Nacmias, B, Tedde, A, Cellini, E, leo, P, Orlacchio, A, Guarnieri, B M, Petruzzi, C, D'Andrea, F, Serio, A, Sorbi, S

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Clinical and genetic analysis of an Italian family with machado-joseph disease von FORLEO, Paolo, CELLINI, Elena, PARNETTI, Lucilla, MURASECCO, Donatella, GALLAI, Virgilio, NACMIAS, Benedetta, SORBI, Sandro

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Association between 5-HT(2A) receptor polymorphism and psychotic symptoms in Alzheimer's disease von Nacmias, B, Tedde, A, Forleo, P, Piacentini, S, Guarnieri, B M, Bartoli, A, Ortenzi, L, Petruzzi, C, Serio, A, Marcon, G, Sorbi, S

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APP717 and Alzheimer's disease in Italy von Sorbi, Sandro, Nacmias, Benedetta, Forleo, Paolo, Piacentini, Silvia, Amaducci, Luigi, Provinciali, Leandro

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