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Page 1
Seizures and EEG features in 74 patients with genetic-dysmorphic syndromes.
Alfei E, Raviglione F, Franceschetti S, D'Arrigo S, Milani D, Selicorni A, Riva D, Zuffardi O, Pantaleoni C, Binelli S. Alfei E, et al. Among authors: binelli s. Am J Med Genet A. 2014 Dec;164A(12):3154-61. doi: 10.1002/ajmg.a.36746. Epub 2014 Sep 24. Am J Med Genet A. 2014. PMID: 25257908
ICTAL EEG fast activity in West syndrome: from onset to outcome.
Panzica F, Binelli S, Canafoglia L, Casazza M, Freri E, Granata T, Avanzini G, Franceschetti S. Panzica F, et al. Among authors: binelli s. Epilepsia. 2007 Nov;48(11):2101-10. doi: 10.1111/j.1528-1167.2007.01264.x. Epub 2007 Sep 6. Epilepsia. 2007. PMID: 17825076 Free article.
GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease-study protocol and preliminary results.
Bersano A, Bedini G, Nava S, Acerbi F, Sebastiano DR, Binelli S, Franceschetti S, Faragò G, Grisoli M, Gioppo A, Ferroli P, Bruzzone MG, Riva D, Ciceri E, Pantaleoni C, Saletti V, Esposito S, Nardocci N, Zibordi F, Caputi L, Marzoli SB, Zedde ML, Pavanello M, Raso A, Capra V, Pantoni L, Sarti C, Pezzini A, Caria F, Dell' Acqua ML, Zini A, Baracchini C, Farina F, Sanguigni S, De Lodovici ML, Bono G, Capone F, Di Lazzaro V, Lanfranconi S, Toscano M, Di Piero V, Sacco S, Carolei A, Toni D, Paciaroni M, Caso V, Perrone P, Calloni MV, Romani A, Cenzato M, Fratianni A, Ciusani E, Prontera P, Lasserve ET, Blecharz K, Vajkoczy P, Parati EA; GEN-O-MA study group. Bersano A, et al. Among authors: binelli s. Neurol Sci. 2019 Mar;40(3):561-570. doi: 10.1007/s10072-018-3664-z. Epub 2019 Jan 3. Neurol Sci. 2019. PMID: 30604336
Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutations.
Canafoglia L, Gilioli I, Invernizzi F, Sofia V, Fugnanesi V, Morbin M, Chiapparini L, Granata T, Binelli S, Scaioli V, Garavaglia B, Nardocci N, Berkovic SF, Franceschetti S. Canafoglia L, et al. Among authors: binelli s. Neurology. 2015 Jul 28;85(4):316-24. doi: 10.1212/WNL.0000000000001784. Epub 2015 Jun 26. Neurology. 2015. PMID: 26115733 Free PMC article.
Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome.
Luisa SF, Rizzo A, Bedini G, Capone F, Di Lazzaro V, Nava S, Acerbi F, Rossi DS, Binelli S, Faragò G, Gioppo A, Grisoli M, Bruzzone MG, Ferroli P, Pantaleoni C, Caputi L, Gomez JV, Parati EA, Bersano A. Luisa SF, et al. Among authors: binelli s. Int J Mol Sci. 2018 Nov 20;19(11):3675. doi: 10.3390/ijms19113675. Int J Mol Sci. 2018. PMID: 30463371 Free PMC article.
51 results