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Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment.
Guerreiro MM, Andermann E, Guerrini R, Dobyns WB, Kuzniecky R, Silver K, Van Bogaert P, Gillain C, David P, Ambrosetto G, Rosati A, Bartolomei F, Parmeggiani A, Paetau R, Salonen O, Ignatius J, Borgatti R, Zucca C, Bastos AC, Palmini A, Fernandes W, Montenegro MA, Cendes F, Andermann F. Guerreiro MM, et al. Among authors: parmeggiani a. Ann Neurol. 2000 Jul;48(1):39-48. Ann Neurol. 2000. PMID: 10894214
Cortical reflex myoclonus in Rett syndrome.
Guerrini R, Bonanni P, Parmeggiani L, Santucci M, Parmeggiani A, Sartucci F. Guerrini R, et al. Among authors: parmeggiani l, parmeggiani a. Ann Neurol. 1998 Apr;43(4):472-9. doi: 10.1002/ana.410430410. Ann Neurol. 1998. PMID: 9546328
The syndrome of polymicrogyria, thalamic hypoplasia, and epilepsy with CSWS.
Bartolini E, Falchi M, Zellini F, Parrini E, Grisotto L, Cosottini M, Posar A, Parmeggiani A, Ambrosetto G, Ferrari AR, Santucci M, Salas-Puig J, Barba C, Guerrini R. Bartolini E, et al. Among authors: parmeggiani a. Neurology. 2016 Mar 29;86(13):1250-9. doi: 10.1212/WNL.0000000000002526. Epub 2016 Mar 4. Neurology. 2016. PMID: 26944271
Autism, macrocrania and epilepsy: how are they linked?
Parmeggiani A, Posar A, Giovanardi-Rossi P, Andermann F, Zifkin B. Parmeggiani A, et al. Brain Dev. 2002 Aug;24(5):296-9. doi: 10.1016/s0387-7604(02)00063-3. Brain Dev. 2002. PMID: 12142067
Co-occurring malformations of cortical development and SCN1A gene mutations.
Barba C, Parrini E, Coras R, Galuppi A, Craiu D, Kluger G, Parmeggiani A, Pieper T, Schmitt-Mechelke T, Striano P, Giordano F, Blumcke I, Guerrini R. Barba C, et al. Among authors: parmeggiani a. Epilepsia. 2014 Jul;55(7):1009-19. doi: 10.1111/epi.12658. Epub 2014 Jun 5. Epilepsia. 2014. PMID: 24902755 Free article.
Posterior fossa malformations and epilepsy.
Parmeggiani A, Posar A, Scaduto MC, Chiodo S, Santucci M, Rossi PG. Parmeggiani A, et al. J Child Neurol. 1999 Feb;14(2):113-7. doi: 10.1177/088307389901400209. J Child Neurol. 1999. PMID: 10073433 Review.
366 results