M. Viri

发表

Inter-rater reliability of the EEG reading in patients with childhood idiopathic epilepsy

Ettore Beghi, Umberto Balottin, R. Borgatti, 2005, Epilepsy Research.

PRRT2 Mutations are the major cause of benign familial infantile seizures

P. Striano, U. Stephani, P. Bauer, 2012, Human mutation.

A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome)

P. Striano, A. Coppola, G. Rubboli, 2008, Epilepsia.

Seizure and EEG Patterns in Angelman's Syndrome

G. Lanzi, F. Lalatta, A. Selicorni, 1995, Journal of child neurology.

Mild Lafora disease: Clinical, neurophysiologic, and genetic findings

R. Michelucci, F. Villani, J. Serratosa, 2014, Epilepsia.

Infantile spasms combined with partial seizures: electroclinical study of eleven cases

M. Viri, A. Romeo, M. Mastrangelo, 1994, The Italian Journal of Neurological Sciences.

A nationwide study on Sydenham's chorea: Clinical features, treatment and prognostic factors.

P. Striano, R. Consolini, A. Capuano, 2021, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

The epileptology of Aicardi-Goutières syndrome: electro-clinical-radiological findings

A. Pichiecchio, L. Chiapparini, S. Orcesi, 2020, Seizure.

Concurrent nocturnal and diurnal paroxysmal dystonia

P. Veggiotti, G. Lanzi, M. Viri, 1993, Child's Nervous System.

Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences

F. Zara, A. Gambardella, A. Labate, 2012, Epilepsia.

Peripheral Markers of the γ-Aminobutyric Acid (GABA)ergic System in Angelman's Syndrome

R. Borgatti, M. Elia, S. Musumeci, 2003 .

The Usefulness of a Targeted Next Generation Sequencing Gene Panel in Providing Molecular Diagnosis to Patients With a Broad Spectrum of Neurodevelopmental Disorders

U. Dianzani, I. Rabbone, G. Mandrile, 2022, Frontiers in Genetics.

Diagnostic imaging in 13 cases of Rasmussen's encephalitis: can early MRI suggest the diagnosis?

L. Tassi, R. Spreafico, A. Erbetta, 2003, Neuroradiology.

Seizures and EEG pattern in Kabuki syndrome

C. Parazzini, G. Capovilla, M. Viri, 2010, Brain and Development.

Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus

P. Striano, A. Orsini, A. Verrotti, 2022, Italian Journal of Pediatrics.

Aromatic L-amino Acid Decarboxylase (AADC) deficiency: results from an Italian modified Delphi consensus

P. Striano, A. Orsini, R. Battini, 2021, Italian Journal of Pediatrics.

Linkage Analysis and Disease Models in Benign Familial Infantile Seizures: A Study of 16 Families

P. Striano, J. Prud'homme, F. Zara, 2006, Epilepsia.

Prevalence of Anti‐cardiolipin, Anti‐β2 Glycoprotein I, and Anti‐prothrombin Antibodies in Young Patients with Epilepsy

P. Veggiotti, M. Viri, A. Romeo, 2002, Epilepsia.

Randomized Double-Blind Crossover Study for Evaluating a Probiotic Mixture on Gastrointestinal and Behavioral Symptoms of Autistic Children

N. Vitulo, M. Viri, M. Calgaro, 2022, Journal of clinical medicine.

A Novel Intragenic Deletion in Ophn1 in A Boy with Developmental Delay, Strabismus and Cerebellar Hypoplasia

P. Chiurazzi, D. Milani, M. Viri, 2015 .

No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy

F. Zara, E. Gennaro, M. Elia, 2003, Epilepsy Research.

An Italian consensus on the management of Lennox-Gastaut syndrome

P. Striano, A. Coppola, M. Puligheddu, 2022, Seizure.

Vaccination and occurrence of seizures in SCN1A mutation-positive patients: a multicenter Italian study.

A. Vignoli, P. Veggiotti, A. Verrotti, 2014, Pediatric neurology.

Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance

P. Striano, F. Zara, C. Minetti, 2013, Epilepsia.

Does the co-occurrence of FGFR3 gene mutation in hypochondroplasia, medial temporal lobe dysgenesis, and focal epilepsy suggest a syndrome?

A. Righini, D. Milani, M. Viri, 2014, Pediatric neurology.

Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial

P. Veggiotti, G. Capovilla, M. Viri, 2002, Epilepsy Research.

Impact of Idiopathic Epilepsy on Mothers and Fathers: Strain, Burden of Care, Worries and Perception of Vulnerability

S. Sacchi, M. Viri, A. Romeo, 2007, Epilepsia.

An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy

P. Striano, A. Coppola, F. Zara, 2007, Neurology.

Early-Onset Occipital Idiopathic Epilepsy: A Syndrome To Be Treated?

P. Veggiotti, G. Capovilla, G. Lanzi, 2003, Journal of child neurology.

STXBP1 encephalopathy

P. Striano, K. Sleegers, G. Cantalupo, 2016, Neurology.

Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation

P. Striano, S. Barbieri, L. Tadini, 2016, Brain and Development.

Short and long interval cortical inhibition in patients with Unverricht-Lundborg and Lafora body disease

Federico Zara, Elisa Visani, Laura Canafoglia, 2010, Epilepsy Research.

Congenital muscular dystrophy with muscle inflammation alpha dystroglycan glycosylation defect and no mutation in FKRP gene

N. Bresolin, G. Comi, R. Cagliani, 2006, Journal of the Neurological Sciences.

Neuropsychological and behavioural aspects in children and adolescents with idiopathic epilepsy at diagnosis and after 12 months of treatment

R. Borgatti, E. Beghi, L. Giordano, 2010, Seizure.

Electrical status epilepticus on eye closure: a case report

P. Veggiotti, G. Lanzi, M. Viri, 1992, Neurophysiologie Clinique/Clinical Neurophysiology.

Benign Partial Epilepsies of Adolescence: A Report of 37 New Cases

A. Gambardella, A. Labate, P. Veggiotti, 2001, Epilepsia.

Eating epilepsy characterised by late-onset epileptic spasms in a case of Cri du chat syndrome

D. Milani, M. Viri, A. Romeo, 2015, Seizure.

Anakinra usage in febrile infection related epilepsy syndrome: an international cohort

Elizabeth M. Wells, E. Wirrell, J. Carpenter, 2020, Annals of clinical and translational neurology.

Ictal impending danger – “sixth sense seizures” – in patients with benign focal epileptic seizures of adolescence

Antonio Gambardella, Giuseppe Capovilla, A. Gambardella, 2008, Epilepsy Research.

EEG at onset and MRI predict long-term clinical outcome in Aicardi syndrome

R. Borgatti, A. Pichiecchio, S. Orcesi, 2022, Clinical Neurophysiology.

Electroclinical presentation and genotype–phenotype relationships in patients with Unverricht‐Lundborg disease carrying compound heterozygous CSTB point and indel mutations

R. Michelucci, F. Zara, S. Franceschetti, 2012, Epilepsia.

Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome

C. Walsh, Ming-Hui Chen, S. Robertson, 2005, Neurology.

Lacosamide in pediatric and adult patients: Comparison of efficacy and safety

P. Striano, O. Bruni, S. Savasta, 2013, Seizure.

Novel mutations of ubiquitin protein ligase 3A gene in Italian patients with Angelman syndrome

A. Selicorni, M. Viri, A. Romeo, 2000, Human mutation.

PRRT2 Mutations are the major cause of benign familial infantile seizures

P. Striano, U. Stephani, P. Bauer, 2012, Human mutation.