Lack of association between ubiquitin carboxy-terminal hydrolase l1 gene polymorphism and PD von SAVETTIERI, G, DE MARCO, E. V, CIVITELLI, D, SALEMI, G, NICOLETTI, G, ANNESI, G, CANDIANO, I. C, QUATTRONE, A

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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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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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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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LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease von Civitelli, D, Tarantino, P, Nicoletti, G, Cirò Candiano, IC, Annesi, F, De Marco, EV, Carrideo, S, Rocca, FE, Condino, F, Spadafora, P, Pugliese, P, D'Asero, S, Morelli, M, Paglionico, S, Annesi, G, Quattrone, A

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Gene dosage influences the age at onset of SCA2 in a family from southern Italy von Spadafora, P, Annesi, G, Liguori, M, Tarantino, P, Cutuli, N, Carrideo, S, Candiano, IC Cirò, Marco, EV De, Civitelli, D, Annesi, F, Giuffrida, S, Quattrone, A

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The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease von Oliveri, Rosario L., Annesi, Grazia, Zappia, Mario, Civitelli, Donatella, De Marco, Elvira V., Pasqua, Angela A., Annesi, Ferdinanda, Spadafora, Patrizia, Gambardella, Antonio, Nicoletti, Giuseppe, Branca, Damiano, Caracciolo, Manuela, Aguglia, Umberto, Quattrone, Aldo

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Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease von Sidransky, E, Nalls, M.A, Aasly, J.O, Aharon-Peretz, J, Annesi, G, Barbosa, E.R, Bar-Shira, A, Berg, D, Bras, J, Brice, A, Chen, C.-M, Clark, L.N, Condroyer, C, De Marco, E.V, Dürr, A, Eblan, M.J, Fahn, S, Farrer, M.J, Fung, H.-C, Gan-Or, Z, Gasser, T, Gershoni-Baruch, R, Giladi, N, Griffith, A, Gurevich, T, Januario, C, Kropp, P, Lang, A.E, Lee-Chen, G.-J, Lesage, S, Marder, K, Mata, I.F, Mirelman, A, Mitsui, J, Mizuta, I, Nicoletti, G, Oliveira, C, Ottman, R, Orr-Urtreger, A, Pereira, L.V, Quattrone, A, Rogaeva, E, Rolfs, A, Rosenbaum, H, Rozenberg, R, Samii, A, Samaddar, T, Schulte, C, Sharma, M, Singleton, A, Spitz, M, Tan, E.-K, Tayebi, N, Toda, T, Troiano, A.R, Tsuji, S, Wittstock, M, Wolfsberg, T.G, Wu, Y.-R, Zabetian, C.P, Zhao, Y, Ziegler, S.G

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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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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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A Novel Exon 1 Mutation in a Patient with Atypical Lafora Progressive Myoclonus Epilepsy Seen as Childhood‐onset Cognitive Deficit von Annesi, Grazia, Sofia, Vito, Gambardella, Antonio, Candiano, Innocenza C. Cirò, Spadafora, Patrizia, Annesi, Ferdinanda, Cutuli, Nunzio, De Marco, Elvira V., Civitelli, Donatella, Carrideo, Sara, Tarantino, Patrizia, Barone, Rita, Zappia, Mario, Quattrone, Aldo

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Neuronal activity is required for the development of specific cortical interneuron subtypes von De Marco García, Natalia V., Karayannis, Theofanis, Fishell, Gord

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A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension von QUATTRONE, A, GAMBARDELLA, A, DIMINNO, G, CARBONE, A. M, OLIVERI, R. L, LAVANO, A, DE MARCO, E. V, CIVITELLI, D, BONO, F, ZAPPIA, M, PARDATSCHER, K

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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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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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Hyperhomocysteinemia is associated with cognitive impairment in multiple sclerosis von Russo, C., Morabito, F., Luise, F., Piromalli, A., Battaglia, L., Vinci, A., Trapani Lombardo, V., de Marco, V., Morabito, P., Condino, F., Quattrone, A., Aguglia, U.

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Evaluation of the suitability of a partially defatted black soldier fly (Hermetia illucens L.) larvae meal as ingredient for rainbow trout (Oncorhynchus mykiss Walbaum) diets von Renna, M, Schiavone, A, Gai, F, Dabbou, S, Lussiana, C, Malfatto, V, Prearo, M, Capucchio, M T, Biasato, I, Biasibetti, E, De Marco, M, Brugiapaglia, A, Zoccarato, I, Gasco, L

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