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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1984 1
1985 1
1987 1
1990 1
1992 2
1993 3
1994 1
1995 2
1998 1
1999 2
2000 1
2002 1
2003 2
2005 1
2006 1
2007 3
2008 2
2009 4
2010 4
2011 2
2012 2
2013 1
2014 3
2015 4
2016 1
2017 2
2018 2
2019 2
2024 0

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51 results

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Page 1
Movement-activated cortical myoclonus in Dravet syndrome.
Canafoglia L, Ragona F, Panzica F, Piazza E, Freri E, Binelli S, Scaioli V, Avanzini G, Granata T, Franceschetti S. Canafoglia L, et al. Among authors: binelli s. Epilepsy Res. 2017 Feb;130:47-52. doi: 10.1016/j.eplepsyres.2017.01.007. Epub 2017 Jan 19. Epilepsy Res. 2017. PMID: 28126647
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: binelli 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.
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.
Adult onset myoclonic Huntington's disease.
Carella F, Scaioli V, Ciano C, Binelli S, Oliva D, Girotti F. Carella F, et al. Among authors: binelli s. Mov Disord. 1993 Apr;8(2):201-5. doi: 10.1002/mds.870080216. Mov Disord. 1993. PMID: 8474490
A novel phenotype of sporadic Creutzfeldt-Jakob disease.
Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, Grisoli M, Binelli S, Fociani P, Bugiani O, Tagliavini F. Giaccone G, et al. Among authors: binelli s. J Neurol Neurosurg Psychiatry. 2007 Dec;78(12):1379-82. doi: 10.1136/jnnp.2007.115444. J Neurol Neurosurg Psychiatry. 2007. PMID: 18024694 Free PMC article.
Intrauterine growth in the offspring of epileptic mothers.
Battino D, Granata T, Binelli S, Caccamo ML, Canevini MP, Canger R, Croci D, Fumarola C, Mai R, Molteni F, et al. Battino D, et al. Among authors: binelli s. Acta Neurol Scand. 1992 Dec;86(6):555-7. doi: 10.1111/j.1600-0404.1992.tb05485.x. Acta Neurol Scand. 1992. PMID: 1481639
Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy.
Busolin G, Malacrida S, Bisulli F, Striano P, Di Bonaventura C, Egeo G, Pasini E, Cianci V, Ferlazzo E, Bianchi A, Coppola G, Elia M, Mecarelli O, Gobbi G, Casellato S, Marchini M, Binelli S, Freri E, Granata T, Posar A, Parmeggiani A, Vigliano P, Boniver C, Aguglia U, Striano S, Tinuper P, Giallonardo AT, Michelucci R, Nobile C. Busolin G, et al. Among authors: binelli s. Epilepsy Res. 2011 Mar;94(1-2):110-6. doi: 10.1016/j.eplepsyres.2011.01.010. Epub 2011 Feb 18. Epilepsy Res. 2011. PMID: 21333500
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
51 results