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Author Details

Maurizio Viri
"Fatebenefratelli e Oftalmico" Hospital
1992
43
21
PMIDPaper TitleJournal TitlePublished Year
38007340Corrigendum to "Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation" [Brain Dev. 38(1) (2016) 128-131].Brain Dev2024
38088023Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing.Epilepsia2024
34768201A nationwide study on Sydenham's chorea: Clinical features, treatment and prognostic factors.Eur J Paediatr Neurol2022
36142909Randomized Double-Blind Crossover Study for Evaluating a Probiotic Mixture on Gastrointestinal and Behavioral Symptoms of Autistic Children.J Clin Med2022
36035117The Usefulness of a Targeted Next Generation Sequencing Gene Panel in Providing Molecular Diagnosis to Patients With a Broad Spectrum of Neurodevelopmental Disorders.Front Genet2022
36030575EEG at onset and MRI predict long-term clinical outcome in Aicardi syndrome.Clin Neurophysiol2022
34806981Video game-induced reflex seizures via a smartphone.Epileptic Disord2022
33506622Anakinra usage in febrile infection related epilepsy syndrome: an international cohort.Ann Clin Transl Neurol2020
26212315Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation.Brain Dev2016
26865513STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy.Neurology2016
26552563Eating epilepsy characterised by late-onset epileptic spasms in a case of Cri du chat syndrome.Seizure2015
24405698Vaccination and occurrence of seizures in SCN1A mutation-positive patients: a multicenter Italian study.Pediatr Neurol2014
25270369Mild Lafora disease: clinical, neurophysiologic, and genetic findings.Epilepsia2014
24630288Does the co-occurrence of FGFR3 gene mutation in hypochondroplasia, medial temporal lobe dysgenesis, and focal epilepsy suggest a syndrome?Pediatr Neurol2014
23298605Lacosamide in pediatric and adult patients: comparison of efficacy and safety.Seizure2013
23360469Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.Epilepsia2013
22623405PRRT2 mutations are the major cause of benign familial infantile seizures.Hum Mutat2012
23205931Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.Epilepsia2012
23126439Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences.Epilepsia2012
22464827Seizures and EEG patterns in Pallister-Killian syndrome: 13 new Italian patients.Eur J Paediatr Neurol2012
20061104Seizures and EEG pattern in Kabuki syndrome.Brain Dev2010
20732824Neuropsychological and behavioural aspects in children and adolescents with idiopathic epilepsy at diagnosis and after 12 months of treatment.Seizure2010
20117916Short and long interval cortical inhibition in patients with Unverricht-Lundborg and Lafora body disease.Epilepsy Res2010
18313902Ictal impending danger--"sixth sense seizures"--in patients with benign focal epileptic seizures of adolescence.Epilepsy Res2008
18248445A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome).Epilepsia2008
17559570Impact of idiopathic epilepsy on mothers and fathers: strain, burden of care, worries and perception of vulnerability.Epilepsia2007
17636062An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy.Neurology2007
16386759Congenital muscular dystrophy with muscle inflammation alpha dystroglycan glycosylation defect and no mutation in FKRP gene.J Neurol Sci2006
16822249Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.Epilepsia2006
15668422Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome.Neurology2005
16118044Inter-rater reliability of the EEG reading in patients with childhood idiopathic epilepsy.Epilepsy Res2005
12684722Diagnostic imaging in 13 cases of Rasmussen's encephalitis: can early MRI suggest the diagnosis?Neuroradiology2003
12661944Early-onset occipital idiopathic epilepsy: a syndrome to be treated?J Child Neurol2003
12661934Peripheral markers of the gamma-aminobutyric acid (GABA)ergic system in Angelman's syndrome.J Child Neurol2003
12694927No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy.Epilepsy Res2003
11879387Prevalence of anti-cardiolipin, anti-beta2 glycoprotein I, and anti-prothrombin antibodies in young patients with epilepsy.Epilepsia2002
11948006Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial.Epilepsy Res2002
11879365Benign partial epilepsies of adolescence: a report of 37 new cases.Epilepsia2001
10737998Novel mutations of ubiquitin protein ligase 3A gene in Italian patients with Angelman syndrome.Hum Mutat2000
8576558Seizure and EEG patterns in Angelman's syndrome.J Child Neurol1995
7721549Infantile spasms combined with partial seizures: electroclinical study of eleven cases.Ital J Neurol Sci1994
8124672Concurrent nocturnal and diurnal paroxysmal dystonia.Childs Nerv Syst1993
1406542Electrical status epilepticus on eye closure: a case report.Neurophysiol Clin1992
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Collaborators

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Co-authored papers 4
Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico
Co-authored papers 4
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Co-authored papers 2
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University of Maryland School of Medicine
Co-authored papers 1
University of Glasgow
Co-authored papers 1
Baylor College of Medicine
Co-authored papers 1
Great Ormond Street Hospital
Co-authored papers 1
Broad Institute of MIT and Harvard
Co-authored papers 1
Vrije Universiteit Brussel
Co-authored papers 1
Jan and Dan Duncan Neurological Research Institute, Baylor College of Medicine
Co-authored papers 1
Baylor College of Medicine
Co-authored papers 1
Prince Sultan Military Medical City
Co-authored papers 1
University of Ottawa
Co-authored papers 1
Alberta Children's Hospital
Co-authored papers 1
Co-authored papers 1
Great Ormond Street Hospital for Children
Co-authored papers 1
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Co-authored papers 1
UCL Institute of Neurology
Co-authored papers 1
New York-Presbyterian Hospital
Co-authored papers 1
Children's National Hospital
Co-authored papers 1
Seattle Children's Hospital, University of Washington
Co-authored papers 1
Texas Children's Hospital
Co-authored papers 1
Fondazione IRCCS Istituto Neurologico Carlo Besta
Co-authored papers 1
Children's Hospital Medical Center, University of Nebraska
Co-authored papers 1
IRCCS Mondino Foundation
Co-authored papers 1
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Boston Children's Hospital, Harvard Medical School
Co-authored papers 1