about
Withdrawal of antiepileptic drugs: guidelines of the Italian League Against EpilepsyUnstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1Tubular proteinuria in mice and humans lacking the intrinsic lysosomal protein SCARB2/Limp-2Lateralizing value of the auditory aura in partial seizures.LGI1 microdeletion in autosomal dominant lateral temporal epilepsy.MicroRNA profiles in hippocampal granule cells and plasma of rats with pilocarpine-induced epilepsy--comparison with human epileptic samples.Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases.Sudden falls due to seizure-induced cardiac asystole in drug-resistant focal epilepsy.A PTG variant contributes to a milder phenotype in Lafora diseaseIdentification of miRNAs differentially expressed in human epilepsy with or without granule cell pathology.A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy.The prevention of neural complications in the surgical treatment of scoliosis: the role of the neurophysiological intraoperative monitoring.LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.Lateral temporal lobe epilepsies: clinical and genetic features.Progressive myoclonic epilepsies: definitive and still undetermined causes.Genetics of epilepsy and relevance to current practice.Epilepsy in primary cerebral tumors: the characteristics of epilepsy at the onset (results from the PERNO study--Project of Emilia Romagna Region on Neuro-Oncology).Impact of treatment on the short-term prognosis of status epilepticus in two population-based cohorts.A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.Increased expression of LGI1 gene triggers growth inhibition and apoptosis of neuroblastoma cells.Intraoperative monitoring of somatosensory (SSEPs) and transcranial electric motor-evoked potentials (tce-MEPs) during surgical correction of neuromuscular scoliosis in patients with central or peripheral nervous system diseases.Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1.Effects of levetiracetam on EEG abnormalities in juvenile myoclonic epilepsy.Clinical course and variability of non-Rasmussen, nonstroke motor and sensory epilepsia partialis continua: a European survey and analysis of 65 cases.Seizure outcome of surgical treatment of focal epilepsy associated with low-grade tumors in children.Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation.Telephone-induced seizures: a new type of reflex epilepsy.A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy.Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.Seizure outcome in surgically treated drug-resistant mesial temporal lobe epilepsy based on the recent histopathological classifications.Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families.A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures.Oligodendroglial hamartoma: a potential source of misdiagnosis for oligodendroglioma.BRAF V600E mutation in neocortical posterior temporal epileptogenic gangliogliomas.Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations.Adult-onset Rasmussen's encephalitis: anatomical-electrographic-clinical features of 7 Italian cases.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Roberto Michelucci
@ast
Roberto Michelucci
@en
Roberto Michelucci
@es
Roberto Michelucci
@nl
Roberto Michelucci
@sl
type
label
Roberto Michelucci
@ast
Roberto Michelucci
@en
Roberto Michelucci
@es
Roberto Michelucci
@nl
Roberto Michelucci
@sl
prefLabel
Roberto Michelucci
@ast
Roberto Michelucci
@en
Roberto Michelucci
@es
Roberto Michelucci
@nl
Roberto Michelucci
@sl
P106
P1153
7005403451
P21
P31
P496
0000-0002-9655-7940