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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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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Modelling seasonal variations of natural radionuclides in agricultural soils von Guagliardi, I., Buttafuoco, G., Ricca, N., Cipriani, M. G., Civitelli, D., Froio, R., Gabriele, A. L., Rosa, R. De

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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: 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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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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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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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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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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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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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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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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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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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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Association of tau gene polymorphism with Parkinson's disease von Zappia, M, Annesi, G, Nicoletti, G, Serra, P, Arabia, G, Pugliese, P, Messina, D, Caracciolo, M, Romeo, N, Annesi, F, Pasqua, A A, Spadafora, P, Civitelli, D, Epifanio, A, Morgante, L, Quattrone, A

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Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis von CALABRO, V, MASON, P. J, FILOSA, S, CIVITELLI, D, CITTADELLA, R, TAGARELLI, A, MARTINI, G, BRANCATI, C, LUZZATTO, L

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Clinical and Genetic Findings in 26 Italian Patients with Lafora Disease von Franceschetti, Silvana, Gambardella, Antonio, Canafoglia, Laura, Striano, Pasquale, Lohi, Hannes, Gennaro, Elena, Ianzano, Leonarda, Veggiotti, Pierangelo, Sofia, Vito, Biondi, Roberto, Striano, Salvatore, Gellera, Cinzia, Annesi, Grazia, Madia, Francesca, Civitelli, Donata, Rocca, Francesca E., Quattrone, Aldo, Avanzini, Giuliano, Minassian, Berge, Zara, Federico

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Magnetic resonance enterography, small-intestine contrast US, and capsule endoscopy to evaluate the small bowel in pediatric Crohn’s disease: a prospective, blinded, comparison stu... von Aloi, Marina, MD, PhD, Di Nardo, Giovanni, MD, PhD, Romano, Giusy, MD, Casciani, Emanuele, MD, Civitelli, Fortunata, MD, Oliva, Salvatore, MD, Viola, Franca, MD, Maccioni, Francesca, MD, Gualdi, Gianfranco, MD, Cucchiara, Salvatore, MD, PhD

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