Development of bioactive electrospun scaffolds suitable to support skin fibroblasts and release Lucilia sericata maggot excretion/secretion von Giacaman, Annesi G., Styliari, Ioanna D., Taresco, Vincenzo, Pritchard, David, Alexander, Cameron, Rose, Felicity R. A. J.

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Met158 variant of the catechol-O-methyltransferase genotype is associated with thicker cortex in adult brain von Cerasa, A, Cherubini, A, Quattrone, A, Gioia, M.C, Tarantino, P, Annesi, G, Assogna, F, Caltagirone, C, Spalletta, G

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A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 von GAMBARDELLA, A, ANNESI, G, ZAPPIA, M, BALLABIO, A, CASARI, G, QUATTRONE, A, DE FUSCO, M, PATRIGNANI, A, AGUGLIA, U, ANNESI, F, PASQUA, A. A, SPADAFORA, P, OLIVERI, R. L, VALENTINE, P

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Association study between the LINGO1 gene and Parkinson’s disease in the Italian population von Annesi, F, De Marco, E.V, Rocca, F.E, Nicoletti, A, Pugliese, P, Nicoletti, G, Arabia, G, Tarantino, P, De Mari, M, Lamberti, P, Gallerini, S, Marconi, R, Epifanio, A, Morgante, L, Cozzolino, A, Barone, P, Torchia, G, Zappia, M, Annesi, G, Quattrone, A

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DJ-1 is a Parkinson's disease susceptibility gene in southern Italy von De Marco, EV, Annesi, G, Tarantino, P, Nicoletti, G, Civitelli, D, Messina, D, Annesi, F, Arabia, G, Salsone, M, Condino, F, Novellino, F, Provenzano, G, Rocca, FE, Colica, C, Morelli, M, Scornaienchi, V, Greco, V, Giofrè, L, Quattrone, A

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The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individuals von Cerasa, A., Gioia, M. C., Tarantino, P., Labate, A., Arabia, G., Annesi, G., Lanza, P., Di Palma, G., Blasi, V., Quattrone, A.

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Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson disease von Tarantino, P, Annesi, F, Scornaienchi, V, Rocca, F E, De Marco, E V, Civitelli, D, Provenzano, G, Sproviero, W, Greco, V, Annesi, G

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Novel human pathological mutations. Gene symbol: PINK1. Disease: Parkinson disease von Scornaienchi, V, Nicoletti, G, Annesi, F, Civitelli, D, De Marco, E V, Provenzano, G, Greco, V, Tarantino, P, Rocca, F E, Annesi, G

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Alpha-synuclein promoter haplotypes and dementia in Parkinson's Disease von De Marco, E.V., Tarantino, P., Rocca, F.E., Provenzano, G., Civitelli, D., De Luca, V., Annesi, F., Carrideo, S., Cirò Candiano, I.C., Romeo, N., Nicoletti, G., Marconi, R., Novellino, F., Morelli, M., Quattrone, A., Annesi, G.

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SIL1 and SARA2 mutations in Marinesco-Sjögren and chylomicron retention diseases von Annesi, G, Aguglia, U, Tarantino, P, Annesi, F, De Marco, EV, Civitelli, D, Torroni, A, Quattrone, A

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Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy von Provenzano, Giovanni, Mannarino, E, Annesi, F, De Marco, E V, Rocca, F E, Greco, V, Scornaienchi, V, Tarantino, P, Civitelli, D, Quattrone, A, Tortorella, G, Annesi, G

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Early-onset SCA17 with 43 TBP repeats: expanding the phenotype? von Tremolizzo, L., Curtò, N. A., Marzorati, L., Lanzani, F., Tarantino, P., Annesi, G., Ferrarese, C.

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Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD von OLIVERI, R. L, ANNESI, G, ANDREOLI, V, GAMBARDELLA, A, AGUGLIA, U, QUATTRONE, A, ZAPPIA, M, CIVITELLI, D, MONTESANTI, R, BRANCA, D, NICOLETTI, G, SPADAFORA, P, PASQUA, A. A, CITTADELLA, R

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Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism von Quadri, Marialuisa, Fang, Mingyan, Picillo, Marina, Olgiati, Simone, Breedveld, Guido J., Graafland, Josja, Wu, Bin, Xu, Fengping, Erro, Roberto, Amboni, Marianna, Pappatà, Sabina, Quarantelli, Mario, Annesi, Grazia, Quattrone, Aldo, Chien, Hsin F., Barbosa, Egberto R., Oostra, Ben A., Barone, Paolo, Wang, Jun, Bonifati, Vincenzo

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DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex von Annesi, Grazia, Savettieri, Giovanni, Pugliese, Pierfrancesco, D'Amelio, Marco, Tarantino, Patrizia, Ragonese, Paolo, La Bella, Vincenzo, Piccoli, Tommaso, Civitelli, Donatella, Annesi, Ferdinanda, Fierro, Brigida, Piccoli, Federico, Arabia, Gennarina, Caracciolo, Manuela, Cirò Candiano, Innocenza Claudia, Quattrone, Aldo

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NACP-REP1 polymorphism is not involved in Parkinson's disease: a case-control study in a population sample from southern Italy von Spadafora, P., Annesi, G., Pasqua, A.A., Serra, P., Cirò Candiano, I.C., Carrideo, S., Tarantino, P., Civitelli, D., De Marco, E.V., Nicoletti, G., Annesi, F., Quattrone, A.

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The fragile X premutation presenting as postprandial hypotension von PUGLIESE, P, ANNESI, G, QUATTRONE, A, CUTULI, N, ARABIA, G, NICOLETTI, G, ANNESI, F, TARANTINO, P, GAMBARDELLA, A, VALENTINO, P, ZAPPIA, M

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Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease von Tarantino, Patrizia, Cirò Candiano, I C, Annesi, F, Rocca, F E, Carrideo, S, Provenzano, G, Civitelli, D, De Marco, E V, Quattrone, A, Annesi, G

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Dopamine D 2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD von Oliveri, R.L., Annesi, G., Zappia, M., Civitelli, D., Montesanti, R., Branca, D., Nicoletti, G., Spadafora, P., Pasqua, A.A., Cittadella, R., Andreoli, V., Gambardella, A., Aguglia, U., Quattrone, A.

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Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease von Cirò Candiano, Innocenza Claudia, Annesi, F, Rocca, E F, Carrideo, S, Tarantino, P, Provenzano, G, Civitelli, D, De Marco, E V, Quattrone, A, Annesi, G

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