Sfoglia per Autore
Evidence of genetic heterogeneity in families with febrile seizures
2000-01-01 Gambardella, A.; Annesi, G.; Foraboschi, P.; Labate, A.; Tomaino, C.; Pasqua, A.
Benign partial epilepsies of adolescence: a report of 37 new cases
2001-01-01 Capovilla, G; Gambardella, A; Romeo, A; Beccaria, F; Montagnini, A; Viri, M; Sgrò, V; Veggiotti, P; Labate, A
Juvenile Huntington's disease presenting as progressive myoclonic epilepsy
2001-01-01 Gambardella, A; Muglia, M.; Labate, A.; Magariello, A.; Gabriele, Al.; Mazzei, R.; Pirritano, D.; Conforti, Fl.; Patitucci, A.; Valentino, P.; Zappia, M.; 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 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
Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH
2001-01-01 Quattrone, A; Bono, F; Oliveri, Rl; Gambardella, A; Pirritano, D; Labate, A; Lucisano, A; Valentino, P; Zappia, M; Aguglia, U; Lavano, A; Fera, F; Pardatscher, K
Silent celiac disease in patients with childhood localization-related epilepsies
2001-01-01 Labate, A; Messina, D; Tammaro, S; LE PIANE, E; Pirritano, D; Cosco, C; Mazzei, R; Oliveri, Rl; Bosco, D; Zappia, M; Aguglia, U; Quattrone, A.; Valentino, Paola; Doldo, P; Gambardella, Antonio
Silent coeliac disease in patients with childhood localization-related epilepsies
2001-01-01 Labate, A; Gambardella, A.; Messina, D.; Tammaro, S.; LE PIANE, E.; Pirritano, D.; Cosco, C.; Doldo, P.; Mazzei, R.; Oliveti, R. L.; Bosco, D.; Zappia, M.; Valentino, P.; Aguglia, U.; 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
Cerebral venous thrombosis and isolated intracrania hypertension without papilledema in CDH
2001-01-01 Quattrone, A; Bono, F; Oliveri, Rl; Gambardella, A; Pirritano, D; Labate, A; Lucisano, A; Valentino, P; Zappia, M; Aguglia, U; Lavano, A; Fera, F; Pardatscher, K
The parkin gene is not involved in late-onset Parkinson’s disease
2001-01-01 Oliveri, Rl; Zappia, M; Annesi, G; Bosco, D; Annesi, F; Spadafora, P; Pasqua, Aa; Tomaino, C; Nicoletti, G; Pirritano, D; Labate, A; Logroscino, G; Manobianca, G; Epifanio, A; Morgante, L; Savettieri, G; Quattrone, A; Gambardella, A
Temporal lobe epilepsy as a unique manifestation of multiple sclerosis
2003-01-01 Gambardella, A; Valentino, P; Labate, A; Sibilia, G; Ruscica, F; Colosimo, E; Nistico, R; Messina, D; Zappia, M; Quattrone, A.
Prodynophin gene promoter polymorphism and temporal lobe epilepsy
2003-01-01 Gambardella, A.; Manna, I.; Labate, A; Chifari, R.; Serra, P.; LA RUSSA, A.; LE PIANE, E.; Cittadella, R.; Andreoli, V.; Sasanelli, F.; Zappia, M.; Aguglia, U.; Quattrone, A.
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy
2003-01-01 Manna, I; Labate, A; Chifari, R; Serra, P; LA RUSSA, A; Lepiane, E; Cittadella, R; Andreoli, V; Sasanelli, F; Zappia, M; Aguglia, U; Quattrone, A; Gambardella, A
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy
2003-01-01 Gambardella, A; Manna, I; Chifari, R; LA RUSSA, A; Serra, P; Cittadella, R; Bonavita, S; Andreoli, V; Lepiane, E; Sasanelli, F; Aguglia, U; A., Gambardella; Labate, A; Gambardella, A
Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus
2003-01-01 Annesi, G; Carrideo, S; Incorpora, G; Pasqua, Aa; Civitelli, D; Polizzi, A; Annesi, F; Spadafora, P; Tarantino, P; CIRO CANDIANO IC, ; Romeo, N; DE MARCO EV, ; Ventura, P; Lepiane, E; Zappia, M; Aguglia, Umberto; Pavone, L; Quattrone, A; Gambardella, A; Labate, A
Startle epilepsy complicating aspartylglucosaminuria
2004-01-01 Labate, A; Barone, R; Gambardella, A; Civitelli, D; Fiumara, A; Annesi, G; Zappia, M; Pavone, L; Quattrone, A.
GENE CONVERSION EVENTS IN ADULT-ONSET SPINAL MUSCOLAR ATROPHY
2004-01-01 Mazzei, M; Gambardella, A; Conforti, Fl; Magariello, A; Patitucci, A; Gabriele, Al; Sprovieri, T; Labate, A; Valentino, P; Bono, F; Bonavita, S; Zappia, M; Muglia, M; Quattrone, A.
Temporal lobe Dysembryoplastic Neuroepithelial Tumour: significance of discordant interictal spikes
2004-01-01 Labate, A; R. S., Briellmann; A. S., Harvey; S. F., Berkovic; P., Federico; R. M., Kalnins; G. C., Fabinyi; G. D., Jackson
ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy
2005-01-01 Gambardella, A; Aguglia, U; Chifari, R; Labate, A; Manna, I; Serra, P; Romeo, N; Sibilia, G; Lepiane, E; Russa, Al; Ventura, P; Cittadella, R; Sasanelli, F; Colosimo, E; Leggio, U; Zappia, M; Quattrone, A
Identification of an Nav1.1 sodium channel (SCN1A) loos-of-function mutation associated with familial simple febrile seizures
2005-01-01 Mantegazza, M.; Gambardella, A.; Rusconi, R.; Schiavon, E.; Annesi, F.; Cassulini, R. R.; Labate, A; Carrideo, S.; Chiari, R.; Canevini, M. P.; Canger, R.; Franceschetti, S.; Annesi, G.; Wanke, E.; Quattrone, A.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Evidence of genetic heterogeneity in families with febrile seizures | 1-gen-2000 | Gambardella, A.; Annesi, G.; Foraboschi, P.; Labate, A.; Tomaino, C.; Pasqua, A. | |
Benign partial epilepsies of adolescence: a report of 37 new cases | 1-gen-2001 | Capovilla, G; Gambardella, A; Romeo, A; Beccaria, F; Montagnini, A; Viri, M; Sgrò, V; Veggiotti, P; Labate, A | |
Juvenile Huntington's disease presenting as progressive myoclonic epilepsy | 1-gen-2001 | Gambardella, A; Muglia, M.; Labate, A.; Magariello, A.; Gabriele, Al.; Mazzei, R.; Pirritano, D.; Conforti, Fl.; Patitucci, A.; Valentino, P.; Zappia, M.; 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 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 | |
Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH | 1-gen-2001 | Quattrone, A; Bono, F; Oliveri, Rl; Gambardella, A; Pirritano, D; Labate, A; Lucisano, A; Valentino, P; Zappia, M; Aguglia, U; Lavano, A; Fera, F; Pardatscher, K | |
Silent celiac disease in patients with childhood localization-related epilepsies | 1-gen-2001 | Labate, A; Messina, D; Tammaro, S; LE PIANE, E; Pirritano, D; Cosco, C; Mazzei, R; Oliveri, Rl; Bosco, D; Zappia, M; Aguglia, U; Quattrone, A.; Valentino, Paola; Doldo, P; Gambardella, Antonio | |
Silent coeliac disease in patients with childhood localization-related epilepsies | 1-gen-2001 | Labate, A; Gambardella, A.; Messina, D.; Tammaro, S.; LE PIANE, E.; Pirritano, D.; Cosco, C.; Doldo, P.; Mazzei, R.; Oliveti, R. L.; Bosco, D.; Zappia, M.; Valentino, P.; Aguglia, U.; 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 | |
Cerebral venous thrombosis and isolated intracrania hypertension without papilledema in CDH | 1-gen-2001 | Quattrone, A; Bono, F; Oliveri, Rl; Gambardella, A; Pirritano, D; Labate, A; Lucisano, A; Valentino, P; Zappia, M; Aguglia, U; Lavano, A; Fera, F; Pardatscher, K | |
The parkin gene is not involved in late-onset Parkinson’s disease | 1-gen-2001 | Oliveri, Rl; Zappia, M; Annesi, G; Bosco, D; Annesi, F; Spadafora, P; Pasqua, Aa; Tomaino, C; Nicoletti, G; Pirritano, D; Labate, A; Logroscino, G; Manobianca, G; Epifanio, A; Morgante, L; Savettieri, G; Quattrone, A; Gambardella, A | |
Temporal lobe epilepsy as a unique manifestation of multiple sclerosis | 1-gen-2003 | Gambardella, A; Valentino, P; Labate, A; Sibilia, G; Ruscica, F; Colosimo, E; Nistico, R; Messina, D; Zappia, M; Quattrone, A. | |
Prodynophin gene promoter polymorphism and temporal lobe epilepsy | 1-gen-2003 | Gambardella, A.; Manna, I.; Labate, A; Chifari, R.; Serra, P.; LA RUSSA, A.; LE PIANE, E.; Cittadella, R.; Andreoli, V.; Sasanelli, F.; Zappia, M.; Aguglia, U.; Quattrone, A. | |
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy | 1-gen-2003 | Manna, I; Labate, A; Chifari, R; Serra, P; LA RUSSA, A; Lepiane, E; Cittadella, R; Andreoli, V; Sasanelli, F; Zappia, M; Aguglia, U; Quattrone, A; Gambardella, A | |
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy | 1-gen-2003 | Gambardella, A; Manna, I; Chifari, R; LA RUSSA, A; Serra, P; Cittadella, R; Bonavita, S; Andreoli, V; Lepiane, E; Sasanelli, F; Aguglia, U; A., Gambardella; Labate, A; Gambardella, A | |
Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus | 1-gen-2003 | Annesi, G; Carrideo, S; Incorpora, G; Pasqua, Aa; Civitelli, D; Polizzi, A; Annesi, F; Spadafora, P; Tarantino, P; CIRO CANDIANO IC, ; Romeo, N; DE MARCO EV, ; Ventura, P; Lepiane, E; Zappia, M; Aguglia, Umberto; Pavone, L; Quattrone, A; Gambardella, A; Labate, A | |
Startle epilepsy complicating aspartylglucosaminuria | 1-gen-2004 | Labate, A; Barone, R; Gambardella, A; Civitelli, D; Fiumara, A; Annesi, G; Zappia, M; Pavone, L; Quattrone, A. | |
GENE CONVERSION EVENTS IN ADULT-ONSET SPINAL MUSCOLAR ATROPHY | 1-gen-2004 | Mazzei, M; Gambardella, A; Conforti, Fl; Magariello, A; Patitucci, A; Gabriele, Al; Sprovieri, T; Labate, A; Valentino, P; Bono, F; Bonavita, S; Zappia, M; Muglia, M; Quattrone, A. | |
Temporal lobe Dysembryoplastic Neuroepithelial Tumour: significance of discordant interictal spikes | 1-gen-2004 | Labate, A; R. S., Briellmann; A. S., Harvey; S. F., Berkovic; P., Federico; R. M., Kalnins; G. C., Fabinyi; G. D., Jackson | |
ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy | 1-gen-2005 | Gambardella, A; Aguglia, U; Chifari, R; Labate, A; Manna, I; Serra, P; Romeo, N; Sibilia, G; Lepiane, E; Russa, Al; Ventura, P; Cittadella, R; Sasanelli, F; Colosimo, E; Leggio, U; Zappia, M; Quattrone, A | |
Identification of an Nav1.1 sodium channel (SCN1A) loos-of-function mutation associated with familial simple febrile seizures | 1-gen-2005 | Mantegazza, M.; Gambardella, A.; Rusconi, R.; Schiavon, E.; Annesi, F.; Cassulini, R. R.; Labate, A; Carrideo, S.; Chiari, R.; Canevini, M. P.; Canger, R.; Franceschetti, S.; Annesi, G.; Wanke, E.; Quattrone, A. |
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