about
Oral-facial-digital syndrome type VI: is C5orf42 really the major gene?Headache in epilepsy: prevalence and clinical featuresUnusual phenotype of glucose transport protein type 1 deficiency syndrome: A case report and literature review.Neuropsychological implications of adjunctive levetiracetam in childhood epilepsyIctal and nonictal paroxysmal events in infantile neuroaxonal dystrophy: polygraphic study of a case.Telogen effluvium caused by magnesium valproate and lamotrigine.Epilepsy and EEG paroxysmal abnormalities in autism spectrum disorders.Sleep-related hypermotor seizures in aspartylglucosaminuria: a case report.Bilateral centrotemporal spikes triggered by blinking: an unusual form of sensory input with related cortical EEG activity.Autism and coeliac disease.Epilepsy in patients with pervasive developmental disorder not otherwise specified.Methyl-CpG-binding protein 2 (MECP2) gene mutations in an Italian sample of patients with pervasive developmental disorder and mental retardation.Breathing instability in Joubert syndromePrognostic factors in patients with mesial temporal lobe epilepsyFamilial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A MutationsNo evidence of GABRG2 mutations in severe myoclonic epilepsy of infancyCarnitine disposition before and during valproate therapy in patients with epilepsy
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Margherita Santucci
@ast
Margherita Santucci
@en
Margherita Santucci
@es
Margherita Santucci
@nl
type
label
Margherita Santucci
@ast
Margherita Santucci
@en
Margherita Santucci
@es
Margherita Santucci
@nl
prefLabel
Margherita Santucci
@ast
Margherita Santucci
@en
Margherita Santucci
@es
Margherita Santucci
@nl
P106
P1153
7102828233
P31
P496
0000-0002-2320-1433