Authors: Borgatti, R Piccinelli, P Passoni, D Dalpra, L Miozzo, M Micheli, R Gagliardi, C Balottin, U

Citation: R. Borgatti et al., Relationship between clinical and genetic features in "inverted duplicatedchromosome 15" patients, PED NEUROL, 24(2), 2001, pp. 111-116

Authors: Capovilla, G Montagnini, A Borgatti, R Piccinelli, P Giordano, L Accorsi, P Caudana, R

Citation: G. Capovilla et al., Seckel's syndrome and malformations of cortical development: Report of three new cases and review of the literature, J CHILD NEU, 16(5), 2001, pp. 382-386

Authors: Borgatti, R Zucca, C Piccinelli, P Macchi, HF Radice, L Tofani, A Benti, R Triulzi, F

Citation: R. Borgatti et al., Unilateral periventricular nodular heterotopia associated with diffuse areas of cerebral functional abnormalities, J CHILD NEU, 15(9), 2000, pp. 622-626

Authors: Piccinelli, P Borgatti, R Perucca, E Tofani, A Donati, G Balottin, U

Citation: P. Piccinelli et al., Frontal nonconvulsive status epilepticus associated with high-dose tiagabine therapy in a child with familial bilateral perisylvian polymicrogyria, EPILEPSIA, 41(11), 2000, pp. 1485-1488

Authors: Borgatti, R Triulzi, F Zucca, C Piccinelli, P Balottin, U Carrozzo, R Guerrini, R

Citation: R. Borgatti et al., Bilateral perisylvian polymicrogyria in three generations, NEUROLOGY, 52(9), 1999, pp. 1910-1913