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Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.
Dazzo E, Fanciulli M, Serioli E, Minervini G, Pulitano P, Binelli S, Di Bonaventura C, Luisi C, Pasini E, Striano S, Striano P, Coppola G, Chiavegato A, Radovic S, Spadotto A, Uzzau S, La Neve A, Giallonardo AT, Mecarelli O, Tosatto SC, Ottman R, Michelucci R, Nobile C. Dazzo E, et al. Among authors: striano p, striano s. Am J Hum Genet. 2015 Jun 4;96(6):992-1000. doi: 10.1016/j.ajhg.2015.04.020. Am J Hum Genet. 2015. PMID: 26046367 Free PMC article.
Tiagabine in glial tumors.
Striano S, Striano P, Boccella P, Nocerino C, Bilo L. Striano S, et al. Among authors: striano p. Epilepsy Res. 2002 Mar;49(1):81-5. doi: 10.1016/s0920-1211(02)00005-0. Epilepsy Res. 2002. PMID: 11948010
Eyelid myoclonia with absences: an overlooked epileptic syndrome?
Striano S, Striano P, Nocerino C, Boccella P, Bilo L, Meo R, Ruosi P. Striano S, et al. Among authors: striano p. Neurophysiol Clin. 2002 Nov;32(5):287-96. doi: 10.1016/s0987-7053(02)00343-x. Neurophysiol Clin. 2002. PMID: 12490326
Suppression of myoclonus in SCA2 by piracetam.
De Rosa A, Striano P, Barbieri F, de Falco A, Rinaldi C, Tucci T, Striano S, Filla A, De Michele G. De Rosa A, et al. Among authors: striano p, striano s. Mov Disord. 2006 Jan;21(1):116-8. doi: 10.1002/mds.20683. Mov Disord. 2006. PMID: 16149096
850 results