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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.
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. |
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Opzioni
Scopri
Tipologia
- 1 Contributo su Rivista 473
- 1 Contributo su Rivista::1.1 Arti... 473
Data di pubblicazione
- In corso di stampa 1
- 2020 - 2024 99
- 2010 - 2019 203
- 2000 - 2009 104
- 1990 - 1999 65
- 1989 - 1989 1
Rivista
- EPILEPSIA 79
- NEUROLOGY 51
- EPILEPSY & BEHAVIOR 17
- EPILEPSY RESEARCH 17
- NEUROLOGICAL SCIENCES 17
- SEIZURE 15
- BRAIN 14
- ANNALS OF NEUROLOGY 11
- MOVEMENT DISORDERS 10
- EUROPEAN JOURNAL OF NEUROLOGY 9
Keyword
- Humans 14
- Epilepsy 13
- epilepsy 13
- temporal lobe epilepsy 11
- Temporal lobe epilepsy 10
- Adult 9
- Female 9
- MRI 9
- Male 8
- Middle Aged 6
Lingua
- eng 446
- ita 1
- scc 1
Accesso al fulltext
- no fulltext 473