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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
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
Benign myoclonic epilepsy: long-term follow-up of 11 new cases.
Rossi PG, Parmeggiani A, Posar A, Santi A, Santucci M. Rossi PG, et al. Among authors: parmeggiani a. Brain Dev. 1997 Nov;19(7):473-9. doi: 10.1016/s0387-7604(97)00060-0. Brain Dev. 1997. PMID: 9408594 Clinical Trial.
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.
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
EEG features and epilepsy in patients with autism.
Rossi PG, Parmeggiani A, Bach V, Santucci M, Visconti P. Rossi PG, et al. Among authors: parmeggiani a. Brain Dev. 1995 May-Jun;17(3):169-74. doi: 10.1016/0387-7604(95)00019-8. Brain Dev. 1995. PMID: 7573755
374 results