Publications by authors named "Simona Binelli"

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Correction: Sciacca, F. L., et al. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome. Int. J. Mol. Sci. 2018, 19, 3675.
Francesca Luisa Sciacca, Ambra Rizzo, Gloria Bedini, Fioravante Capone, Vincenzo Di Lazzaro, Simona Binelli

Int J Mol Sci· December 2019

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GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease-study protocol and preliminary results.
Anna Bersano, Gloria Bedini, Sara Nava, Francesco Acerbi, Davide Rossi Sebastiano, Simona Binelli

Neurol Sci· March 2019

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Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome.
Sciacca Francesca Luisa, Ambra Rizzo, Gloria Bedini, Fioravante Capone, Vincenzo Di Lazzaro, Simona Binelli

Int J Mol Sci· November 2018

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Pediatric NMDAR encephalitis: A single center observation study with a closer look at movement disorders.
Tiziana Granata, Sara Matricardi, Francesca Ragona, Elena Freri, Federica Zibordi, Simona Binelli

Eur J Paediatr Neurol· March 2018

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The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations.
Roberto Michelucci, Patrizia Pulitano, Carlo Di Bonaventura, Simona Binelli, Concetta Luisi

Epilepsy Behav· March 2017

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Movement-activated cortical myoclonus in Dravet syndrome.
Laura Canafoglia, Francesca Ragona, Ferruccio Panzica, Elena Piazza, Elena Freri, Simona Binelli

Epilepsy Res· February 2017

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PARADISE 24 instrument: An observational study on psychosocial difficulties, quality of life, and disability levels in patients with epilepsy.
Rui Quintas, Milda Cerniauskaite, Ambra Mara Giovannetti, Silvia Schiavolin, Alberto Raggi, Simona Binelli

Epilepsy Behav· November 2016

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Electroencephalographic (EEG) Photoparoxysmal Responses Under 5 Years of Age: Diagnostic Implications and Peculiarities.
Simona Binelli, Francesca Ragona, Laura Canafoglia, Elena Freri, Veronica Saletti

J Child Neurol· November 2015

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Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutations.
Laura Canafoglia, Isabella Gilioli, Federica Invernizzi, Vito Sofia, Valeria Fugnanesi, Simona Binelli

Neurology· July 2015

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Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.
Emanuela Dazzo, Manuela Fanciulli, Elena Serioli, Giovanni Minervini, Patrizia Pulitano, Simona Binelli

Am J Hum Genet· June 2015

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Focal seizure, focal dyskinesia, or both? A complex motor phenomenon reveals anti-NMDAR encephalitis.
Elena Freri, Sara Matricardi, Mara Patrini, Simona Binelli, Francesca Andreetta

Seizure· April 2015

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Seizures and EEG features in 74 patients with genetic-dysmorphic syndromes.
Enrico Alfei, Federico Raviglione, Silvana Franceschetti, Stefano D'Arrigo, Donatella Milani, Simona Binelli

Am J Med Genet A· December 2014

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Refractory absence epilepsy and glut1 deficiency syndrome: a new case report and literature review.
Francesca Ragona, Sara Matricardi, Barbara Castellotti, Mara Patrini, Elena Freri, Simona Binelli

Neuropediatrics· October 2014

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Comprehensive educational plan for patients with epilepsy and comorbidity (EDU-COM): a pragmatic randomised trial.
Simone Beretta, Ettore Beghi, Paolo Messina, Francesca Gerardi, Francesca Pescini, Simona Binelli

J Neurol Neurosurg Psychiatry· August 2014

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Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.
Roberto Michelucci, Elena Pasini, Sandro Malacrida, Pasquale Striano, Carlo Di Bonaventura, Simona Binelli

Epilepsia· July 2013

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ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy.
Laura Rigon, Andrea Vettori, Giorgia Busolin, Gabriella Egeo, Patrizia Pulitano, Simona Binelli

Epilepsy Res Treat· August 2012

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Paroxysmal non-epileptic motor events in childhood: a clinical and video-EEG-polymyographic study.
Carlotta Canavese, Laura Canafoglia, Caterina Costa, Federica Zibordi, Giovanna Zorzi, Simona Binelli

Dev Med Child Neurol· April 2012

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Focal epilepsies in adult patients attending two epilepsy centers: classification of drug-resistance, assessment of risk factors, and usefulness of "new" antiepileptic drugs.
Isabella Gilioli, Aglaia Vignoli, Elisa Visani, Marina Casazza, Laura Canafoglia, Simona Binelli

Epilepsia· April 2012

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Immunotherapy responsive startle with antibodies to voltage gated potassium channels.
Carlo Antozzi, Simona Binelli, Carolina Frassoni, Claudia Ciano, Angela Vincent

BMJ Case Rep· November 2011

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A novel phenotype of sporadic Creutzfeldt-Jakob disease.
G Giaccone, Giuseppe Di Fede, Michela Mangieri, Lucia Limido, Raffaella Capobianco, Simona Binelli

BMJ Case Rep· November 2011

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Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy.
Giorgia Busolin, Sandro Malacrida, Francesca Bisulli, Pasquale Striano, Carlo Di Bonaventura, Simona Binelli

Epilepsy Res· March 2011

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Myoclonus in Creutzfeldt-Jakob disease: polygraphic and video-electroencephalography assessment of 109 patients.
Simona Binelli, Pamela Agazzi, Laura Canafoglia, Vidmer Scaioli, Ferruccio Panzica

Mov Disord· December 2010

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Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients.
Francesca Ragona, Daniela Brazzo, Ilaria De Giorgi, Monica Morbi, Elena Freri, Simona Binelli

Brain Dev· January 2010

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Sleep-related tongue biting may not be a sign of epilepsy: a case of sleep-related faciomandibular myoclonus.
Suela Dylgjeri, Alessandro Pincherle, Claudia Ciano, Simona Binelli, Flavio Villani

Epilepsia· January 2009

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Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins.
Erica Diani, Carlo Di Bonaventura, Oriano Mecarelli, Antonio Gambardella, Maurizio Elia, Simona Binelli

Epilepsy Res· July 2008

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