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Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution.
Agostinelli, S; Traverso, M; Accorsi, P; Beccaria, F; Belcastro, V; Capovilla, G; Cappanera, S; Coppola, A; Dalla Bernardina, B; Darra, F; Ferretti, M; Elia, M; Galeone, D; Giordano, L; Gobbi, G; Nicita, F; Parisi, P; Pezzella, M; Spalice, A; Striano, S; Tozzi, E; Vignoli, A; Minetti, C; Zara, F; Striano, P; Verrotti, A.
Affiliation
  • Agostinelli S; Department of Pediatrics, University of Chieti, Chieti, Italy. sergio_agostinelli@yahoo.it
Eur J Neurol ; 20(5): 856-9, 2013 May.
Article in En | MEDLINE | ID: mdl-23020086
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy, Absence / Glucose Transporter Type 1 / Anticonvulsants / Mutation Type of study: Observational_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans / Male Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2013 Type: Article Affiliation country: Italy
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy, Absence / Glucose Transporter Type 1 / Anticonvulsants / Mutation Type of study: Observational_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans / Male Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2013 Type: Article Affiliation country: Italy