Renato Borgatti
Department of Child Neuropsychiatry
Eugenio Medea Scientific Institute
Bosisio Parini (Lecco)
Italy
Name/email consistency: high
- A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation. Borgatti, R., Zucca, C., Cavallini, A., Ferrario, M., Panzeri, C., Castaldo, P., Soldovieri, M.V., Baschirotto, C., Bresolin, N., Dalla Bernardina, B., Taglialatela, M., Bassi, M.T. Neurology (2004)
- Study of attentional processes in children with idiopathic epilepsy by Conners' Continuous Performance Test. Borgatti, R., Piccinelli, P., Montirosso, R., Donati, G., Rampani, A., Molteni, L., Tofani, A., Nicoli, F., Zucca, C., Bresolin, N., Balottin, U. J. Child Neurol. (2004)
- Peripheral markers of the gamma-aminobutyric acid (GABA)ergic system in Angelman's syndrome. Borgatti, R., Piccinelli, P., Passoni, D., Romeo, A., Viri, M., Musumeci, S.A., Elia, M., Cogliati, T., Valseriati, D., Grasso, R., Raggi, M.E., Ferrarese, C. J. Child Neurol. (2003)
- Pervasive developmental disorders and GABAergic system in patients with inverted duplicated chromosome 15. Borgatti, R., Piccinelli, P., Passoni, D., Raggi, E., Ferrarese, C. J. Child Neurol. (2001)
- Unilateral periventricular nodular heterotopia associated with diffuse areas of cerebral functional abnormalities. Borgatti, R., Zucca, C., Piccinelli, P., Macchi, H.F., Radice, L., Tofani, A., Benti, R., Triulzi, F. J. Child Neurol. (2000)
