GAMBARDELLA, ANTONIO
GAMBARDELLA, ANTONIO
Dipartimento di Scienze Mediche e Chirurgiche
3-T magnetic resonance imaging simultaneous automated multimodal approach improves detection of ambiguous visual hippocampal sclerosis.
2015-01-01 Vasta, R; Caligiuri, Me; Labate, A; Cherubini, A; Mumoli, L; Ferlazzo, E; Perrotta, P; Lanza, Pl; Augimeri, A; Aguglia, U; Quattrone, A; Gambardella, A
A brainstem hypermetabolism in a patient with essential palatal tremor: A simultaneous 18F-FDG-PET/3 T-MRI study
2021-01-01 Marsico, Oreste; Sammarra, Ilaria; Viola, Pasquale; Pisani, Davide; Trimboli, Michele; Chiarella, Giuseppe; Cascini, Giuseppe Lucio; Labate, Angelo; Gambardella, Antonio
A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video-polygraphic study
2001-01-01 Capovilla, G; Rubboli, G; Beccaria, F; Lorenzetti, Me; Montagnini, A; Resi, C; Gardella, E; Gambardella, A; Romeo, A; Tassinari, Ca
A familial t(4;8) translocation segregates with epilepsy and migraine with aura
2020-01-01 Crippa, M.; Malatesta, P.; Bonati, M. T.; Trapasso, F.; Fortunato, F.; Annesi, G.; Larizza, L.; Labate, A.; Finelli, P.; Perrotti, N.; Gambardella, A.
A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies
2020-01-01 Musumeci, O.; Ferlazzo, E.; Rodolico, C.; Gambardella, A.; Gagliardi, M.; Aguglia, U.; Toscano, A.
A Functional Genetic Variation of the 5-HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy
2012-01-01 Manna, I; Mumoli, L; Palamara, G; Aguglia, U; Quattrone, A; Ferlazzo, E; Labate, A; Gambardella, A
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy
2011-01-01 Manna, I; Gambardella, A; Bianchi, A; Striano, P; Tozzi, R; Aguglia, U; Beccaria, F; Benna, P; Campostrini, R; Canevini, Mp; Condino, F; Durisotti, C; Elia, M; Giallonardo, At; Iudice, A; Labate, A; LA NEVE, A; Michelucci, R; Muscas, Gc; Paravidino, R; Zaccara, G; Zucca, C; Zara, F; Perucca, E
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.
2019-01-01 Berghuis, B; Stapleton, C; Sonsma, Acm; Hulst, J; de Haan, Gj; Lindhout, D; Demurtas, R; Gambardella, A; as member of EpiPGX, Consortium; Krause, R; Depondt, C; Kunz, Ws; Zara, F; Striano, P; Craig, J; Auce, P; Marson, Ag; Stefansson, H; O'Brien, Tj; Johnson, Mr; Sills, Gj; Wolking, S; Lerche, H; Sisodiya, Sm; Sander, Jw; Cavalleri, Gl; Koeleman, Bpc; Mccormack, M.
A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension
1999-01-01 Quattrone, A; Carbone, Am; Oliveri, Rl; Lavano, A; DE MARCO, Ev; Civitelli, D; Bono, F; Zappia, M; Pardatscher, K; Dimimmo, G; Gambardella, A
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3
2002-01-01 M, Muglia; A, Magariello; Nicoletti, G; Patitucci, A; Gabriele, Al; Conforti, Fl; Mazzei, R; Caracciolo, M; Casari, G; Ardito, B; Lastilla, M; Gambardella, A; Quattrone, A.
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability
2018-01-01 Campostrini, G; Di Francesco, Jc; Castellotti, B; Raffaella Milanesi, R; Gnecchi-Ruscone, T; Bonzanni, M; Bucchi, A; Baruscotti, M; Ferrarese, C; Franceschetti, S; Canafoglia, L; Ragona, F; Freri, E; Gambardella, A; Costa, C; Gellera, C; Granata, T; Barbuti, A; Di, Francesco; Labate, A
A new Italian instrument for the assessment of irritability in patients with epilepsy.
2011-01-01 Piazzini, A; Turner, K; Edefonti, V; Bravi, F; Canevini, Mp; LICE Irritability, Group; Ferraroni, M; Chifari, R; Romeo, A; Viri, M; La Neve, A; Francavilla, T; Lamberti, P; Mecarelli, O; Magaudda, A; Gugliotta, C; Gambardella, A; Labate, A; Ferlazzo, E; Rocchi, R; Pucci, B; Vatti, G; Sicilia, I; Iudice, A; Pelliccia, V.
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chomosome 1
2000-01-01 Gambardella, A; Annesi, G; DE FUSCO, M; Patrignani, A; Aguglia, U; Annesi, F; Spadafora, P; Oliveri, Rl; Valentino, P; Zappia, M; Ballabio, A; Et, Al
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1
2000-01-01 Gambardella, A; Annesi, G; DE FUSCO, M; Patrignani, A; Aguglia, U; Annesi, F; Pasqua, Aa; Spadafora, P; Oliveri, Rl; Valentino, P; Zappia, M; Ballabio, A; Casari, G; Quattrone, A.
A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification.
2015-01-01 Gagliardi, M; Annesi, G; Nicoletti, G; Perrotta, P; Pustorino, G; Iannello, G; Tarantino, P; Gambardella, A; Quattrone, A; Morelli, M
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability
2018-01-01 Bonzanni, M; Difrancesco, Jc; Milanesi, R; Campostrini, G; Castellotti, B; Bucchi, A; Baruscotti, M; Ferrarese, C; Franceschetti, S; Canafoglia, L; Ragona, F; Freri, E; Labate, A; Gambardella, A; Costa, C; Rivolta, I; Gellera, C; Granata, T; Barbuti, A; Difrancesco, D
A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit
2004-01-01 Annesi, G; Sofia, V; Gambardella, A; Candiano, Ic; Spadafora, P; Annesi, F; Cutuli, N; DE MARCO, Ev; Civitelli, D; Carrideo, S; Tarantino, P; Barone, R; Zappia, M; Quattrone, A.
A novel ICA-based hardware system for reconfigurable and portable BCI
2009-01-01 Palumbo, A.; Calabrese, B.; Cocorullo, G.; Lanuzza, M.; Veltri, Pierangelo; Vizza, P.; Sturniolo, M.; Gambardella, A
A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings
2001-01-01 Oliveri, Rl; Muglia, M; De Stefano, N; Mazzei, R; Labate, A; Conforti, Fl; Patitucci, A; Gabriele, Al; Tagarelli, G; Magariello, A; Zappia, M; Gambardella, A; Federico, A; Quattrone, A
A novel mutation in the notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and MRI spectroscopic analyses
2001-01-01 Oliveri, R. L.; Muglia, M; DE STEFANO, N; Mazzei, R; Labate, A; Conforti, F. L.; Patitucci, A; Gabriele, A. L.; Magariello, A; Zappia, M; Gambardella, A; Federico, A; Quattrone, A
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 3-T magnetic resonance imaging simultaneous automated multimodal approach improves detection of ambiguous visual hippocampal sclerosis. | 1-gen-2015 | Vasta, R; Caligiuri, Me; Labate, A; Cherubini, A; Mumoli, L; Ferlazzo, E; Perrotta, P; Lanza, Pl; Augimeri, A; Aguglia, U; Quattrone, A; Gambardella, A | |
| A brainstem hypermetabolism in a patient with essential palatal tremor: A simultaneous 18F-FDG-PET/3 T-MRI study | 1-gen-2021 | Marsico, Oreste; Sammarra, Ilaria; Viola, Pasquale; Pisani, Davide; Trimboli, Michele; Chiarella, Giuseppe; Cascini, Giuseppe Lucio; Labate, Angelo; Gambardella, Antonio | |
| A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video-polygraphic study | 1-gen-2001 | Capovilla, G; Rubboli, G; Beccaria, F; Lorenzetti, Me; Montagnini, A; Resi, C; Gardella, E; Gambardella, A; Romeo, A; Tassinari, Ca | |
| A familial t(4;8) translocation segregates with epilepsy and migraine with aura | 1-gen-2020 | Crippa, M.; Malatesta, P.; Bonati, M. T.; Trapasso, F.; Fortunato, F.; Annesi, G.; Larizza, L.; Labate, A.; Finelli, P.; Perrotti, N.; Gambardella, A. | |
| A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies | 1-gen-2020 | Musumeci, O.; Ferlazzo, E.; Rodolico, C.; Gambardella, A.; Gagliardi, M.; Aguglia, U.; Toscano, A. | |
| A Functional Genetic Variation of the 5-HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy | 1-gen-2012 | Manna, I; Mumoli, L; Palamara, G; Aguglia, U; Quattrone, A; Ferlazzo, E; Labate, A; Gambardella, A | |
| A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy | 1-gen-2011 | Manna, I; Gambardella, A; Bianchi, A; Striano, P; Tozzi, R; Aguglia, U; Beccaria, F; Benna, P; Campostrini, R; Canevini, Mp; Condino, F; Durisotti, C; Elia, M; Giallonardo, At; Iudice, A; Labate, A; LA NEVE, A; Michelucci, R; Muscas, Gc; Paravidino, R; Zaccara, G; Zucca, C; Zara, F; Perucca, E | |
| A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. | 1-gen-2019 | Berghuis, B; Stapleton, C; Sonsma, Acm; Hulst, J; de Haan, Gj; Lindhout, D; Demurtas, R; Gambardella, A; as member of EpiPGX, Consortium; Krause, R; Depondt, C; Kunz, Ws; Zara, F; Striano, P; Craig, J; Auce, P; Marson, Ag; Stefansson, H; O'Brien, Tj; Johnson, Mr; Sills, Gj; Wolking, S; Lerche, H; Sisodiya, Sm; Sander, Jw; Cavalleri, Gl; Koeleman, Bpc; Mccormack, M. | |
| A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension | 1-gen-1999 | Quattrone, A; Carbone, Am; Oliveri, Rl; Lavano, A; DE MARCO, Ev; Civitelli, D; Bono, F; Zappia, M; Pardatscher, K; Dimimmo, G; Gambardella, A | |
| A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3 | 1-gen-2002 | M, Muglia; A, Magariello; Nicoletti, G; Patitucci, A; Gabriele, Al; Conforti, Fl; Mazzei, R; Caracciolo, M; Casari, G; Ardito, B; Lastilla, M; Gambardella, A; Quattrone, A. | |
| A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability | 1-gen-2018 | Campostrini, G; Di Francesco, Jc; Castellotti, B; Raffaella Milanesi, R; Gnecchi-Ruscone, T; Bonzanni, M; Bucchi, A; Baruscotti, M; Ferrarese, C; Franceschetti, S; Canafoglia, L; Ragona, F; Freri, E; Gambardella, A; Costa, C; Gellera, C; Granata, T; Barbuti, A; Di, Francesco; Labate, A | |
| A new Italian instrument for the assessment of irritability in patients with epilepsy. | 1-gen-2011 | Piazzini, A; Turner, K; Edefonti, V; Bravi, F; Canevini, Mp; LICE Irritability, Group; Ferraroni, M; Chifari, R; Romeo, A; Viri, M; La Neve, A; Francavilla, T; Lamberti, P; Mecarelli, O; Magaudda, A; Gugliotta, C; Gambardella, A; Labate, A; Ferlazzo, E; Rocchi, R; Pucci, B; Vatti, G; Sicilia, I; Iudice, A; Pelliccia, V. | |
| A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chomosome 1 | 1-gen-2000 | Gambardella, A; Annesi, G; DE FUSCO, M; Patrignani, A; Aguglia, U; Annesi, F; Spadafora, P; Oliveri, Rl; Valentino, P; Zappia, M; Ballabio, A; Et, Al | |
| A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 | 1-gen-2000 | Gambardella, A; Annesi, G; DE FUSCO, M; Patrignani, A; Aguglia, U; Annesi, F; Pasqua, Aa; Spadafora, P; Oliveri, Rl; Valentino, P; Zappia, M; Ballabio, A; Casari, G; Quattrone, A. | |
| A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification. | 1-gen-2015 | Gagliardi, M; Annesi, G; Nicoletti, G; Perrotta, P; Pustorino, G; Iannello, G; Tarantino, P; Gambardella, A; Quattrone, A; Morelli, M | |
| A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability | 1-gen-2018 | Bonzanni, M; Difrancesco, Jc; Milanesi, R; Campostrini, G; Castellotti, B; Bucchi, A; Baruscotti, M; Ferrarese, C; Franceschetti, S; Canafoglia, L; Ragona, F; Freri, E; Labate, A; Gambardella, A; Costa, C; Rivolta, I; Gellera, C; Granata, T; Barbuti, A; Difrancesco, D | |
| A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit | 1-gen-2004 | Annesi, G; Sofia, V; Gambardella, A; Candiano, Ic; Spadafora, P; Annesi, F; Cutuli, N; DE MARCO, Ev; Civitelli, D; Carrideo, S; Tarantino, P; Barone, R; Zappia, M; Quattrone, A. | |
| A novel ICA-based hardware system for reconfigurable and portable BCI | 1-gen-2009 | Palumbo, A.; Calabrese, B.; Cocorullo, G.; Lanuzza, M.; Veltri, Pierangelo; Vizza, P.; Sturniolo, M.; Gambardella, A | |
| A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings | 1-gen-2001 | Oliveri, Rl; Muglia, M; De Stefano, N; Mazzei, R; Labate, A; Conforti, Fl; Patitucci, A; Gabriele, Al; Tagarelli, G; Magariello, A; Zappia, M; Gambardella, A; Federico, A; Quattrone, A | |
| A novel mutation in the notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and MRI spectroscopic analyses | 1-gen-2001 | Oliveri, R. L.; Muglia, M; DE STEFANO, N; Mazzei, R; Labate, A; Conforti, F. L.; Patitucci, A; Gabriele, A. L.; Magariello, A; Zappia, M; Gambardella, A; Federico, A; Quattrone, A |