about
The Revolution in Migraine Genetics: From Aching Channels Disorders to a Next-Generation MedicineTemporal lobe connects regression and macrocephaly to autism spectrum disordersGain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy.Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish.Autism-epilepsy phenotype with macrocephaly suggests PTEN, but not GLIALCAM, genetic screening.Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations.Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy.Somatic overgrowth predisposes to seizures in autism spectrum disordersOn the application of quantitative EEG for characterizing autistic brain: a systematic reviewMECP2 duplication phenotype in symptomatic females: report of three further cases.Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations.Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype.Targeted Gene Resequencing (Astrochip) to Explore the Tripartite Synapse in Autism-Epilepsy Phenotype with Macrocephaly.Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.Focal cortical dysplasia, microcephaly and epilepsy in a boy with 1q21.1-q21.3 duplication.An integrated EEG and eye-tracking approach for the study of responding and initiating joint attention in Autism Spectrum DisordersSelf-induced multiple comas with recreational baclofen overdoses in an adolescent girl.Fusiform gyrus responses to neutral and emotional faces in children with autism spectrum disorders: a high density ERP study.Internalizing and externalizing symptoms in preschool and school-aged children with epilepsy: Focus on clinical and EEG features.Mosaic mutations of the LIS1 gene cause subcortical band heterotopia.Classification of autism spectrum disorder using supervised learning of brain connectivity measures extracted from synchrostates.Understanding Spreading Depression from Headache to Sudden Unexpected Death.Benign infantile seizures followed by autistic regression in a boy with 16p11.2 deletion.Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1.Late-onset epileptic spasms: clinical evidence and outcome in 34 patients.Mitochondrial respiratory chain defects in skin fibroblasts from patients with Dravet syndrome.Subcortical band heterotopia with simplified gyral pattern and syndactyly.Transient Cognitive Impairment in Epilepsyencephalopathy: A distinctive generalized developmental and epileptic encephalopathyWest syndrome associated with 14q12 duplications harboring FOXG1Phenytoin administration in the newborn and infantEmotional and behavioral problems after pediatric liver transplantation: a quantitative assessmentClinical and electroencephalographic correlates of psychiatric features in children with frontal lobe epilepsyEvolution of Epileptiform Activity in Zebrafish by Statistical-Based Integration of Electrophysiology and 2-Photon Ca2+ ImagingDefining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Federico Sicca
@ast
Federico Sicca
@en
Federico Sicca
@es
Federico Sicca
@nl
Federico Sicca
@sl
type
label
Federico Sicca
@ast
Federico Sicca
@en
Federico Sicca
@es
Federico Sicca
@nl
Federico Sicca
@sl
prefLabel
Federico Sicca
@ast
Federico Sicca
@en
Federico Sicca
@es
Federico Sicca
@nl
Federico Sicca
@sl
P1053
J-7768-2016
P106
P1153
7801420531
P21
P2798
P31
P3829
P496
0000-0002-4917-5253