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Federico Sicca
Federico Sicca
Child and Adolescent Epilepsy Unit - USL Toscana Centro
Bestätigte E-Mail-Adresse bei uslcentro.toscana.it
Titel
Zitiert von
Zitiert von
Jahr
Idiopathic Epilepsies with Seizures Precipitated by Fever and SCN1A Abnormalities
C Marini, D Mei, T Temudo, AR Ferrari, D Buti, C Dravet, AI Dias, ...
Epilepsia 48 (9), 1678-1685, 2007
2332007
SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy
DRM Vlaskamp, BJ Shaw, R Burgess, D Mei, M Montomoli, H Xie, ...
Neurology 92 (2), e96-e107, 2019
1522019
Germline and mosaic mutations of FLN1 in men with periventricular heterotopia
R Guerrini, D Mei, S Sisodiya, F Sicca, B Harding, Y Takahashi, T Dorn, ...
Neurology 63 (1), 51-56, 2004
1522004
Epilepsy and malformations of the cerebral cortex
R Guerrini, F Sicca, L Parmeggiani
Epileptic disorders 5, S9-S26, 2003
1522003
On the application of quantitative EEG for characterizing autistic brain: a systematic review
L Billeci, F Sicca, K Maharatna, F Apicella, A Narzisi, G Campatelli, ...
Frontiers in human neuroscience 7, 442, 2013
1462013
Mosaic mutations of the LIS1 gene cause subcortical band heterotopia
F Sicca, A Kelemen, P Genton, S Das, D Mei, F Moro, WB Dobyns, ...
Neurology 61 (8), 1042-1046, 2003
1302003
Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations
V Cetica, S Chiari, D Mei, E Parrini, L Grisotto, C Marini, D Pucatti, ...
Neurology 88 (11), 1037-1044, 2017
1212017
Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4. 1
F Sicca, P Imbrici, MC D'Adamo, F Moro, F Bonatti, P Brovedani, ...
Neurobiology of disease 43 (1), 239-247, 2011
1212011
Classification of autism spectrum disorder using supervised learning of brain connectivity measures extracted from synchrostates
W Jamal, S Das, IA Oprescu, K Maharatna, F Apicella, F Sicca
Journal of neural engineering 11 (4), 046019, 2014
1182014
Epilepsy, behavioral abnormalities, and physiological comorbidities in syntaxin-binding protein 1 (STXBP1) mutant zebrafish
BP Grone, M Marchese, KR Hamling, MG Kumar, CS Krasniak, F Sicca, ...
PLoS one 11 (3), e0151148, 2016
1062016
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations
N Specchio, C Marini, A Terracciano, D Mei, M Trivisano, F Sicca, L Fusco, ...
Epilepsia 52 (7), 1251-1257, 2011
1042011
Focal seizures with affective symptoms are a major feature of PCDH19 gene–related epilepsy
C Marini, F Darra, N Specchio, D Mei, A Terracciano, L Parmeggiani, ...
Epilepsia 53 (12), 2111-2119, 2012
992012
Fusiform gyrus responses to neutral and emotional faces in children with autism spectrum disorders: a high density ERP study
F Apicella, F Sicca, RR Federico, G Campatelli, F Muratori
Behavioural brain research 251, 155-162, 2013
812013
Genetically induced dysfunctions of Kir2. 1 channels: implications for short QT3 syndrome and autism–epilepsy phenotype
E Ambrosini, F Sicca, MS Brignone, MC D'adamo, C Napolitano, ...
Human Molecular Genetics 23 (18), 4875-4886, 2014
782014
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy
F Sicca, E Ambrosini, M Marchese, L Sforna, I Servettini, G Valvo, ...
Scientific Reports 6 (1), 34325, 2016
712016
Autism-epilepsy phenotype with macrocephaly suggests PTEN, but not GLIALCAM, genetic screening
M Marchese, V Conti, G Valvo, F Moro, F Muratori, R Tancredi, ...
BMC medical genetics 15, 1-7, 2014
682014
An integrated EEG and eye-tracking approach for the study of responding and initiating joint attention in Autism Spectrum Disorders
L Billeci, A Narzisi, A Tonacci, B Sbriscia-Fioretti, L Serasini, F Fulceri, ...
Scientific Reports 7 (1), 13560, 2017
672017
Understanding spreading depression from headache to sudden unexpected death
O Cozzolino, M Marchese, F Trovato, E Pracucci, GM Ratto, MG Buzzi, ...
Frontiers in neurology 9, 333507, 2018
662018
West syndrome associated with 14q12 duplications harboring FOXG1
P Striano, R Paravidino, F Sicca, P Chiurazzi, S Gimelli, A Coppola, ...
Neurology 76 (18), 1600-1602, 2011
632011
Defining the electroclinical phenotype and outcome of PCDH19‐related epilepsy: A multicenter study
M Trivisano, N Pietrafusa, A Terracciano, C Marini, D Mei, F Darra, ...
Epilepsia 59 (12), 2260-2271, 2018
522018
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