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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: tiberti a. Epilepsy Res. 1999 May;35(1):29-37. doi: 10.1016/s0920-1211(98)00124-7. Epilepsy Res. 1999. PMID: 10232792 Clinical Trial.
Lack of SCN1A mutations in familial febrile seizures.
Malacarne M, Madia F, Gennaro E, Vacca D, Güney AI, Buono S, Bernardina BD, Gaggero R, Gobbi G, Lispi ML, Malamaci D, Melideo G, Roccella M, Sferro C, Tiberti A, Vanadia F, Vigevano F, Viri F, Vitali MR, Bricarelli FD, Bianchi A, Zara F. Malacarne M, et al. Among authors: tiberti a. Epilepsia. 2002 May;43(5):559-62. doi: 10.1046/j.1528-1157.2002.29301.x. Epilepsia. 2002. PMID: 12027919 Free article.
Familial Ohtahara syndrome due to a novel ARX gene mutation.
Giordano L, Sartori S, Russo S, Accorsi P, Galli J, Tiberti A, Bettella E, Marchi M, Vignoli A, Darra F, Murgia A, Bernardina BD. Giordano L, et al. Among authors: tiberti a. Am J Med Genet A. 2010 Dec;152A(12):3133-7. doi: 10.1002/ajmg.a.33701. Am J Med Genet A. 2010. PMID: 21108397 Free article.
56 results