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Prospective study of first-line vigabatrin monotherapy in childhood partial epilepsies.
Gobbi G, Pini A, Bertani G, Menegati E, Tiberti A, Valseriati D, Besana D, Rasmini P, Guerrini R, Belmonte A, Veggiotti P, Resi C, Lanzi G, Capovilla G, Galeone D, Milani S. Gobbi G, et al. Among authors: veggiotti p. Epilepsy Res. 1999 May;35(1):29-37. doi: 10.1016/s0920-1211(98)00124-7. Epilepsy Res. 1999. PMID: 10232792 Clinical Trial.
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1.
Gennaro E, Malacarne M, Carbone I, Riggio MC, Bianchi A, Bonanni P, Boniver C, Dalla Bernardina B, De Marco P, Giordano L, Guerrini R, Santorum E, Sebastianelli R, Vecchi M, Veggiotti P, Vigevano F, Bricarelli FD, Zara F. Gennaro E, et al. Among authors: veggiotti p. Epilepsia. 1999 Dec;40(12):1799-803. doi: 10.1111/j.1528-1157.1999.tb01601.x. Epilepsia. 1999. PMID: 10612347 Free article.
The costs of childhood epilepsy in Italy: comparative findings from three health care settings.
Guerrini R, Battini R, Ferrari AR, Veggiotti P, Besana D, Gobbi G, Pezzani M, Berta E, Tetto A, Beghi E, Monticelli ML, Tediosi F, Garattini L, Russo S, Rasmini P, Amadi A, Quarti P, Fabrizzi R; Epilepsy Collaborative Study Group. Guerrini R, et al. Among authors: veggiotti p. Epilepsia. 2001 May;42(5):641-6. doi: 10.1046/j.1528-1157.2001.27300.x. Epilepsia. 2001. PMID: 11380572 Free article.
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.
Nabbout R, Gennaro E, Dalla Bernardina B, Dulac O, Madia F, Bertini E, Capovilla G, Chiron C, Cristofori G, Elia M, Fontana E, Gaggero R, Granata T, Guerrini R, Loi M, La Selva L, Lispi ML, Matricardi A, Romeo A, Tzolas V, Valseriati D, Veggiotti P, Vigevano F, Vallée L, Dagna Bricarelli F, Bianchi A, Zara F. Nabbout R, et al. Among authors: veggiotti p. Neurology. 2003 Jun 24;60(12):1961-7. doi: 10.1212/01.wnl.0000069463.41870.2f. Neurology. 2003. PMID: 12821740
232 results