ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease von Montecchiani, Celeste, Pedace, Lucia, Lo Giudice, Temistocle, Casella, Antonella, Mearini, Marzia, Gaudiello, Fabrizio, Pedroso, José L, Terracciano, Chiara, Caltagirone, Carlo, Massa, Roberto, St George-Hyslop, Peter H, Barsottini, Orlando G P, Kawarai, Toshitaka, Orlacchio, Antonio

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CLINICAL AND GENETIC STUDY OF A JAPANESE FAMILY WITH COMPLICATED HEREDITARY SPASTIC PARAPLEGIA AND ALZHEIMER'S DISEASE von Montecchiani, Celeste, D'Onofrio, Laura, Mearini, Marzia, Gaudiello, Fabrizio, Miele, Marialuisa, Caltagirone, Carlo, Kawarai, Toshitaka, Orlacchio, Antonio

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HEREDITARY SPASTIC PARAPLEGIA AND ALZHEIMER'S DISEASE: HYPOTHESIS OF A FOUNDER EFFECT OF A SPG4/ SPAST MUTATION von Pedace, Lucia, Mearini, Marzia, Casella, Antonella, Montecchiani, Celeste, Miele, Marialuisa, Caltagirone, Carlo, Kawarai, Toshitaka, Orlacchio, Antonio

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P2‐088: Hereditary Spastic Paraplegia and Alzheimer's Disease: Hypothesis of a Founder Effect of a SPG4/Spast Mutation von Pedace, Lucia, Mearini, Marzia, Casella, Antonella, Montecchiani, Celeste, Miele, Marialuisa, Caltagirone, Carlo, Kawarai, Toshitaka, Orlacchio, Antonio

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Hereditary Spastic Paraplegia Type 4 (SPG4): A Clinico-Genetic Study in a Large Cohort of Patients with Spastic Paraplegia (P5.075) von Mearini, Marzia, Pedace, Lucia, Casella, Antonella, Celeste, Montecchiani, Gaudiello, Fabrizio, Miele, Marialuisa, Pedroso, Jose Luiz, Caltagirone, Carlo, Massa, Roberto, Barsottini, Orlando, Munhoz, Renato, Kawarai, Toshitaka, Orlacchio, Antonio

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P1‐054: Clinical and genetic study of a large spg4 italian family with hereditary spastic paraplegia and early‐onset familial Alzheimer's disease von Lo Giudice, Temistocle, Casella, Antonella, Mearini, Marzia, Montecchiani, Celeste, Miele, Marialuisa, Kawarai, Toshitaka, Orlacchio, Antonio

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Clinical and genetic study of a large spg4 italian family with hereditary spastic paraplegia and early-onset familial Alzheimer’s disease von Lo Giudice, Temistocle, Casella, Antonella, Mearini, Marzia, Montecchiani, Celeste, Miele, Marialuisa, Kawarai, Toshitaka, Orlacchio, Antonio

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Identification of ALS5/SPG11/ KIAA1840 Mutations in Patients with Autosomal Recessive Form of Charcot-Marie-Tooth Disease Type 2 (S44.002) von Montecchiani, Celeste, Pedace, Lucia, Lo Giudice, Temistocle, Casella, Antonella, Mearini, Marzia, Gaudiello, Fabrizio, Pedroso, Jose Luiz, Terracciano, Chiara, Caltagirone, Carlo, Massa, Roberto, St George-Hyslop, Peter, Barsottini, Orlando, Kawarai, Toshitaka, Orlacchio, Antonio

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MIR128-1 mediated lysosomal hydrolases down-regulation in monocytes and lymphocytes from Alzheimer's disease patients von Orlacchio, Antonio, Tiribuzi, Roberto, Crispoltoni, Lucia, Mearini, Marzia, Zampolini, Mauro, Datti, Alessandro, Martino, Sabata, Orlacchio, Aldo

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P4‐339: MIR128–1 mediated lysosomal hydrolases down‐regulation in monocytes and lymphocytes from Alzheimer's disease patients von Orlacchio, Antonio, Tiribuzi, Roberto, Crispoltoni, Lucia, Mearini, Marzia, Zampolini, Mauro, Datti, Alessandro, Martino, Sabata, Orlacchio, Aldo

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P1–122: MiR128 up‐regulation correlates with impaired beta‐amyloid 42 degradation in monocytes of patients with sporadic Alzheimer's disease von Tiribuzi, Roberto, Crispoltoni, Lucia, Porcellati, Serena, Mearini, Marzia, Di Lullo, Martina, Florenzano, F., Pirro, Matteo, Bagaglia, Francesco, Palmerini, Carlo, Miele, Marialuisa, Kawarai, Toshitaka, Zampolini, Mauro, Orlacchio, Aldo, Orlacchio, Antonio

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MiR128 up-regulation correlates with impaired beta-amyloid 42 degradation in monocytes of patients with sporadic Alzheimer's disease von Tiribuzi, Roberto, Crispoltoni, Lucia, Porcellati, Serena, Mearini, Marzia, Di Lullo, Martina, Florenzano, F, Pirro, Matteo, Bagaglia, Francesco, Palmerini, Carlo, Miele, Marialuisa, Kawarai, Toshitaka, Zampolini, Mauro, Orlacchio, Aldo, Orlacchio, Antonio

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