TARANTINO, PATRIZIA
TARANTINO, PATRIZIA
Istituto di Bioimmagini e Fisiologia Molecolare - IBFM
An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolate
2015 Quadri, Marialuisa; Yang, Xu; Cossu, Giovanni; Olgiati, Simone; M Saddi, Valeria; J Breedveld, Guido; Ouyang, Limei; Hu, Jingchu; Xu, Na; Graafland, Josja; Ricchi, Valeria; Murgia, Daniela; Correia Guedes, Leonor; Mariani, Claudio; J Marti, Maria; Tarantino, Patrizia; Asselta, Rosanna; Valldeoriola, Francesc; Gagliardi, Monica; Pezzoli, Gianni; Ezquerra, Mario; Quattrone, Aldo; Ferreira, Joaquim; Annesi, Grazia; Goldwurm, Stefano; Tolosa, Eduardo; A Oostra, Ben; Melis, Maurizio; Wang, Jun; Bonifati, Vincenzo
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.
2015 Mumoli, Laura; Tarantino, Patrizia; Michelucci, Roberto; Bianchi, Amedeo; Labate, Angelo; Franceschetti, Silvana; Marini, Carla; Striano, Pasquale; Gagliardi, Monica; Edoardoferlazzo, ; Sofia, Vito; Pennese, Loredana; Annesi, Grazia; Aguglia, Umberto; Guerrini, Renzo; Zara, Federico; Gambardella, Antonio; behalf of the Genetic Commission, On; League Against Epilepsy, Italian
Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia.
2014 Brighina, Laura; Saracchi, Enrico; Ferri, Francesca; Gagliardi, Monica; Tarantino, Patrizia; Morzenti, Sabrina; Musarra, Monica; Patassini, Mirko; Annesi, Grazia; Ferrarese, Carlo
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP.
2013 Labate, A; Tarantino, P; Palamara, G; Gagliardi, M; Cavalcanti, F; Ferlazzo, E; Sturniolo, M; Incorpora, G; Annesi, G; Aguglia, U; Gambardella, A
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP.
2013 Labate A; Tarantino P; Palamara G; Gagliardi M; Cavalcanti F; Ferlazzo E; Sturniolo M; Incorpora G; Annesi G; Aguglia U; Gambardella A.
Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy.
2013 Dibilio, V; Cavalcanti, F; Nicoletti, A; Mostile, G; Bruno, E; Annesi, G; Tarantino, P; Gagliardi, M; Gambardella, A; Quattrone, A; Zappia, M
Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy.
2013 Dibilio V; Cavalcanti F; Nicoletti A; Mostile G; Bruno E; Annesi G; Tarantino P; Gagliardi M; Gambardella A; Quattrone A; Zappia M.
Dentatorubral-pallidoluysian atrophy: haplotype of Asian origin in 2 Italian families
2012 Aridon, P; Tarantino, P; Ragonese, P; D'Amelio, M; Cinturino, A; Salemi, G; Gagliardi, M; Lo Re, V; Scarpitta, A; Gambardella, A; Quattrone, A; Annesi, G; Savettieri, G
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences.
2012 Labate A; Tarantino P; Viri M; Mumoli L; Gagliardi M; Romeo A; Zara F; Annesi G; Gambardella A.
Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism.
2012 Scornaienchi, V; Civitelli, D; De Marco, Ev; Annesi, G; Tarantino, P; Rocca, Fe; Greco, V; Provenzano, G; Annesi, F; Nicoletti, G; Colica, C; Uncini, A; Salsone, M; Novellino, F; Morelli, M; Arabia, G; Gambardella, A; Quattrone, A
Spinocerebellar ataxia type 7: report of a new Italian family.
2012 Italiano, D; Tarantino, P; De Marco, Ev; Calabrò, Rs; Bramanti, P; Quattrone, A; Annesi, G
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy.
2011 Greco, V; De Marco, Ev; Rocca, Fe; Annesi, F; Civitelli, D; Provenzano, G; Tarantino, P; Scornaienchi, V; Pucci, F; Salsone, M; Novellino, F; Morelli, M; Paglionico, S; Gambardella, A; Quattrone, A; Annesi, G
Association study between the LINGO1 gene and Parkinson s disease in the Italian population
2011 Annesi F; De Marco EV; Rocca FE; 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.
Early-onset SCA17 with 43 TBP repeats: expanding the phenotype?
2011 Tremolizzo L; Curtò NA; Marzorati L; Lanzani F; Tarantino P; Annesi G; Ferrarese C.
Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease
2011 Tarantino, P; V De Marco, E; E Rocca, F; Annesi, F; Civitelli, D; Provenzano, G; Scornaienchi, V; Greco, V; Colica, C; Nicoletti, G; Quattrone, A; Annesi, G
Author's reply to the comment of Sironi et al. on "Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism"
2010 Tarantino, Patrizia; Civitelli, Donatella; Annesi, Ferdinanda; De Marco Elvira, V; Rocca Francesca, E; Pugliese, Pierfrancesco; Nicoletti, Giuseppe; Carrideo, Sara; Provenzano, Giovanni; Annesi, Grazia; Quattrone, Aldo
DJ-1 is a Parkinson's disease susceptibility gene in southern Italy.
2010 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
Dysbindin C-A-T haplotype is associated with thicker medial orbitofrontal cortex in healthy population
2010 Cerasa, A; Quattrone, A; Gioia, Mc; Tarantino, P; Annesi, G; Assogna, F; Caltagirone, C; De Luca, V; Spalletta, G
Met 158 variant of the COMT genotype is associated with thicker cortex in adult brain
2010 Cerasa, A; Cherubini, A; Quattrone, A; Gioia, Mc; Tarantino, P; Annesi, G; Assogna, F; Caltagirone, C; Spalletta, G
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism.
2009 Tarantino, P; Civitelli, D; Annesi, F; DE MARCO, ELVIRA VALERIA; Rocca, Fe; Pugliese, P; Nicoletti, G; Carrideo, S; Provenzano, G; Annesi, G; Quattrone, A
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolate | 1-gen-2015 | Quadri, Marialuisa; Yang, Xu; Cossu, Giovanni; Olgiati, Simone; M Saddi, Valeria; J Breedveld, Guido; Ouyang, Limei; Hu, Jingchu; Xu, Na; Graafland, Josja; Ricchi, Valeria; Murgia, Daniela; Correia Guedes, Leonor; Mariani, Claudio; J Marti, Maria; Tarantino, Patrizia; Asselta, Rosanna; Valldeoriola, Francesc; Gagliardi, Monica; Pezzoli, Gianni; Ezquerra, Mario; Quattrone, Aldo; Ferreira, Joaquim; Annesi, Grazia; Goldwurm, Stefano; Tolosa, Eduardo; A Oostra, Ben; Melis, Maurizio; Wang, Jun; Bonifati, Vincenzo | |
| No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy. | 1-gen-2015 | Mumoli, Laura; Tarantino, Patrizia; Michelucci, Roberto; Bianchi, Amedeo; Labate, Angelo; Franceschetti, Silvana; Marini, Carla; Striano, Pasquale; Gagliardi, Monica; Edoardoferlazzo, ; Sofia, Vito; Pennese, Loredana; Annesi, Grazia; Aguglia, Umberto; Guerrini, Renzo; Zara, Federico; Gambardella, Antonio; behalf of the Genetic Commission, On; League Against Epilepsy, Italian | |
| Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia. | 1-gen-2014 | Brighina, Laura; Saracchi, Enrico; Ferri, Francesca; Gagliardi, Monica; Tarantino, Patrizia; Morzenti, Sabrina; Musarra, Monica; Patassini, Mirko; Annesi, Grazia; Ferrarese, Carlo | |
| Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. | 1-gen-2013 | Labate, A; Tarantino, P; Palamara, G; Gagliardi, M; Cavalcanti, F; Ferlazzo, E; Sturniolo, M; Incorpora, G; Annesi, G; Aguglia, U; Gambardella, A | |
| Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. | 1-gen-2013 | Labate A; Tarantino P; Palamara G; Gagliardi M; Cavalcanti F; Ferlazzo E; Sturniolo M; Incorpora G; Annesi G; Aguglia U; Gambardella A. | |
| Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy. | 1-gen-2013 | Dibilio, V; Cavalcanti, F; Nicoletti, A; Mostile, G; Bruno, E; Annesi, G; Tarantino, P; Gagliardi, M; Gambardella, A; Quattrone, A; Zappia, M | |
| Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy. | 1-gen-2013 | Dibilio V; Cavalcanti F; Nicoletti A; Mostile G; Bruno E; Annesi G; Tarantino P; Gagliardi M; Gambardella A; Quattrone A; Zappia M. | |
| Dentatorubral-pallidoluysian atrophy: haplotype of Asian origin in 2 Italian families | 1-gen-2012 | Aridon, P; Tarantino, P; Ragonese, P; D'Amelio, M; Cinturino, A; Salemi, G; Gagliardi, M; Lo Re, V; Scarpitta, A; Gambardella, A; Quattrone, A; Annesi, G; Savettieri, G | |
| Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences. | 1-gen-2012 | Labate A; Tarantino P; Viri M; Mumoli L; Gagliardi M; Romeo A; Zara F; Annesi G; Gambardella A. | |
| Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. | 1-gen-2012 | Scornaienchi, V; Civitelli, D; De Marco, Ev; Annesi, G; Tarantino, P; Rocca, Fe; Greco, V; Provenzano, G; Annesi, F; Nicoletti, G; Colica, C; Uncini, A; Salsone, M; Novellino, F; Morelli, M; Arabia, G; Gambardella, A; Quattrone, A | |
| Spinocerebellar ataxia type 7: report of a new Italian family. | 1-gen-2012 | Italiano, D; Tarantino, P; De Marco, Ev; Calabrò, Rs; Bramanti, P; Quattrone, A; Annesi, G | |
| Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. | 1-gen-2011 | Greco, V; De Marco, Ev; Rocca, Fe; Annesi, F; Civitelli, D; Provenzano, G; Tarantino, P; Scornaienchi, V; Pucci, F; Salsone, M; Novellino, F; Morelli, M; Paglionico, S; Gambardella, A; Quattrone, A; Annesi, G | |
| Association study between the LINGO1 gene and Parkinson s disease in the Italian population | 1-gen-2011 | Annesi F; De Marco EV; Rocca FE; 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. | |
| Early-onset SCA17 with 43 TBP repeats: expanding the phenotype? | 1-gen-2011 | Tremolizzo L; Curtò NA; Marzorati L; Lanzani F; Tarantino P; Annesi G; Ferrarese C. | |
| Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease | 1-gen-2011 | Tarantino, P; V De Marco, E; E Rocca, F; Annesi, F; Civitelli, D; Provenzano, G; Scornaienchi, V; Greco, V; Colica, C; Nicoletti, G; Quattrone, A; Annesi, G | |
| Author's reply to the comment of Sironi et al. on "Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism" | 1-gen-2010 | Tarantino, Patrizia; Civitelli, Donatella; Annesi, Ferdinanda; De Marco Elvira, V; Rocca Francesca, E; Pugliese, Pierfrancesco; Nicoletti, Giuseppe; Carrideo, Sara; Provenzano, Giovanni; Annesi, Grazia; Quattrone, Aldo | |
| DJ-1 is a Parkinson's disease susceptibility gene in southern Italy. | 1-gen-2010 | 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 | |
| Dysbindin C-A-T haplotype is associated with thicker medial orbitofrontal cortex in healthy population | 1-gen-2010 | Cerasa, A; Quattrone, A; Gioia, Mc; Tarantino, P; Annesi, G; Assogna, F; Caltagirone, C; De Luca, V; Spalletta, G | |
| Met 158 variant of the COMT genotype is associated with thicker cortex in adult brain | 1-gen-2010 | Cerasa, A; Cherubini, A; Quattrone, A; Gioia, Mc; Tarantino, P; Annesi, G; Assogna, F; Caltagirone, C; Spalletta, G | |
| Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism. | 1-gen-2009 | Tarantino, P; Civitelli, D; Annesi, F; DE MARCO, ELVIRA VALERIA; Rocca, Fe; Pugliese, P; Nicoletti, G; Carrideo, S; Provenzano, G; Annesi, G; Quattrone, A |