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Human Molecular Genetics|September 11, 2021
Epilepsy-causing Reelin mutations result in impaired secretion and intracellular degradation of mutant proteinsEmanuela Dazzo, Carlo NobileEpilepsia Open|April 24, 2024
A de novo pathogenic variant in MICAL-1 causes epilepsy with auditory featuresPaolo Bonanni, Roberto Giorda, Roberto Michelucci, et al.Current Neurology and Neuroscience Reports|May 24, 2012
Genetics of epilepsy and relevance to current practiceRoberto Michelucci, Elena Pasini, Patrizia Riguzzi, et al.Clinical Neurology and Neurosurgery|May 4, 2018
LGI1 tumor tissue expression and serum autoantibodies in patients with primary malignant gliomaEmanuela Dazzo, Elena Pasini, Sandra Furlan, et al.Plos Genetics|October 21, 2016
Secretion-Positive LGI1 Mutations Linked to Lateral Temporal Epilepsy Impair Binding to ADAM22 and ADAM23 ReceptorsEmanuela Dazzo, Emanuela Leonardi, Elisa Belluzzi, et al.Epilepsy Research|December 10, 2013
Suggestive linkage of familial mesial temporal lobe epilepsy to chromosome 3q26Manuela Fanciulli, Carlo Di Bonaventura, Gabriella Egeo, et al.Epilepsy Research|November 28, 2017
CNTNAP2 mutations and autosomal dominant epilepsy with auditory featuresEmanuela Leonardi, Emanuela Dazzo, Maria Cristina Aspromonte, et al.Epilepsia|July 29, 2015
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsyPasquale Striano, Elena Serioli, Lia Santulli, et al.Annals of Neurology|February 3, 2018
Mutations in MICAL-1cause autosomal-dominant lateral temporal epilepsyEmanuela Dazzo, Kati Rehberg, Roberto Michelucci, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|July 30, 2020
Autosomal dominant lateral temporal lobe epilepsy associated with a novel reelin mutationRoberto Michelucci, Emanuela Dazzo, Lilia Volpi, et al.Pageof 3