Abstracts (HTML) Autorenliste

Accorsi, P.

Repetitive and Stereotyped Behaviors in Neurodevelopmental Disorders: More than a Movement Disorder

Antonarakis, S.

Encephalopathy with Epilepsy and Movement Disorder Related to RNF13: Case Report
Hearing Loss Is Not an Obligatory Hallmark of SPATA5 Early-Onset Epileptic Encephalopathy with Microcephaly and Hypomyelination

Armstrong, J.

Pharmacological Combination of Sodium Channel Blockers (Oxcarbazepine and Lacosamide) to Control Seizures in Two Patients with Neonatal-Onset Epilepsy due to De Novo SCNA2 Heterozygous Mutation

Bastaraud, S. Chantot

Monogenic Chorea Etiologies in Children: A Study of a Cohort of 85 Patients and a Proposal of a Diagnostic Algorithm

Bellini, B.

A Novel X-linked Mutation of CACNA1F Gene in Two Male Siblings Presenting Nystagmus

Benoit, V.

The Neonatal Presentation of BRAT1-Related Neonatal Rigidity and Multifocal Seizure Syndrome

Blanc, X.

Encephalopathy with Epilepsy and Movement Disorder Related to RNF13: Case Report

Bölsterli, B. K.

A Case of Vitamin-B6-Dependent Disorder Presenting with Abnormal Eye–Head Movements and Infantile Spasms without Hypsarrhythmia

Borel, C.

Hearing Loss Is Not an Obligatory Hallmark of SPATA5 Early-Onset Epileptic Encephalopathy with Microcephaly and Hypomyelination

Borras, A.

Pharmacological Combination of Sodium Channel Blockers (Oxcarbazepine and Lacosamide) to Control Seizures in Two Patients with Neonatal-Onset Epilepsy due to De Novo SCNA2 Heterozygous Mutation

Brunetti, S.

Repetitive and Stereotyped Behaviors in Neurodevelopmental Disorders: More than a Movement Disorder

Burglen, L.

Monogenic Chorea Etiologies in Children: A Study of a Cohort of 85 Patients and a Proposal of a Diagnostic Algorithm

Calza, S.

Repetitive and Stereotyped Behaviors in Neurodevelopmental Disorders: More than a Movement Disorder

Caporali, C.

Developmental Profile of an Italian Cohort of ELBW Preterm Infants Born in the 2000s: Is Emerging Language a Weak Point in Early Development?

Chiapparini, L.

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Cilio, M. R.

The Neonatal Presentation of BRAT1-Related Neonatal Rigidity and Multifocal Seizure Syndrome

Danhaive, O.

The Neonatal Presentation of BRAT1-Related Neonatal Rigidity and Multifocal Seizure Syndrome

De Giorgis, V.

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Delgadillo, V.

Pharmacological Combination of Sodium Channel Blockers (Oxcarbazepine and Lacosamide) to Control Seizures in Two Patients with Neonatal-Onset Epilepsy due to De Novo SCNA2 Heterozygous Mutation

Dénervaud, S.

Structural Brain Abnormalities in Epilepsy with Myoclonic Atonic Seizures

De Simone, Micaela

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Doummar, D.

Monogenic Chorea Etiologies in Children: A Study of a Cohort of 85 Patients and a Proposal of a Diagnostic Algorithm

Fazzi, E.

Neurodevelopmental Disorder in Children Affected by Ocular Albinism Type 1
A Novel X-linked Mutation of CACNA1F Gene in Two Male Siblings Presenting Nystagmus

Fazzi, E. M.

Repetitive and Stereotyped Behaviors in Neurodevelopmental Disorders: More than a Movement Disorder
The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Flas, S.

The Neonatal Presentation of BRAT1-Related Neonatal Rigidity and Multifocal Seizure Syndrome

Fluss, J.

Hearing Loss Is Not an Obligatory Hallmark of SPATA5 Early-Onset Epileptic Encephalopathy with Microcephaly and Hypomyelination
Structural Brain Abnormalities in Epilepsy with Myoclonic Atonic Seizures

Fons, C.

Pharmacological Combination of Sodium Channel Blockers (Oxcarbazepine and Lacosamide) to Control Seizures in Two Patients with Neonatal-Onset Epilepsy due to De Novo SCNA2 Heterozygous Mutation

Franzoni, A.

Neurodevelopmental Disorder in Children Affected by Ocular Albinism Type 1

Galli, J.

Repetitive and Stereotyped Behaviors in Neurodevelopmental Disorders: More than a Movement Disorder
Neurodevelopmental Disorder in Children Affected by Ocular Albinism Type 1
A Novel X-linked Mutation of CACNA1F Gene in Two Male Siblings Presenting Nystagmus

Galli, Jessica

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Giordano, L.

Repetitive and Stereotyped Behaviors in Neurodevelopmental Disorders: More than a Movement Disorder
The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Gitti, F.

Repetitive and Stereotyped Behaviors in Neurodevelopmental Disorders: More than a Movement Disorder

Giuliano, F.

A Case of Vitamin-B6-Dependent Disorder Presenting with Abnormal Eye–Head Movements and Infantile Spasms without Hypsarrhythmia

Gonzalez, V.

Pharmacological Combination of Sodium Channel Blockers (Oxcarbazepine and Lacosamide) to Control Seizures in Two Patients with Neonatal-Onset Epilepsy due to De Novo SCNA2 Heterozygous Mutation

Hagmann, P.

Structural Brain Abnormalities in Epilepsy with Myoclonic Atonic Seizures

Hocq, C.

The Neonatal Presentation of BRAT1-Related Neonatal Rigidity and Multifocal Seizure Syndrome

Iascone, M.

A Novel X-linked Mutation of CACNA1F Gene in Two Male Siblings Presenting Nystagmus

Italian AGS Study Group (Members:,

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Izzi, C.

A Novel X-linked Mutation of CACNA1F Gene in Two Male Siblings Presenting Nystagmus

Julia, N.

Pharmacological Combination of Sodium Channel Blockers (Oxcarbazepine and Lacosamide) to Control Seizures in Two Patients with Neonatal-Onset Epilepsy due to De Novo SCNA2 Heterozygous Mutation

Kalser, J.

A Case of Vitamin-B6-Dependent Disorder Presenting with Abnormal Eye–Head Movements and Infantile Spasms without Hypsarrhythmia

Kern, I.

Hearing Loss Is Not an Obligatory Hallmark of SPATA5 Early-Onset Epileptic Encephalopathy with Microcephaly and Hypomyelination

Korff, C.

Encephalopathy with Epilepsy and Movement Disorder Related to RNF13: Case Report
Structural Brain Abnormalities in Epilepsy with Myoclonic Atonic Seizures

La Piana, R.

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Lebon, S.

Structural Brain Abnormalities in Epilepsy with Myoclonic Atonic Seizures

Lederer, D.

The Neonatal Presentation of BRAT1-Related Neonatal Rigidity and Multifocal Seizure Syndrome

Longo, S.

Developmental Profile of an Italian Cohort of ELBW Preterm Infants Born in the 2000s: Is Emerging Language a Weak Point in Early Development?

Louha, M.

Monogenic Chorea Etiologies in Children: A Study of a Cohort of 85 Patients and a Proposal of a Diagnostic Algorithm

Manzoni, F.

Developmental Profile of an Italian Cohort of ELBW Preterm Infants Born in the 2000s: Is Emerging Language a Weak Point in Early Development?

Masnada, Silvia

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Mignot, C.

Monogenic Chorea Etiologies in Children: A Study of a Cohort of 85 Patients and a Proposal of a Diagnostic Algorithm

Molinaro, A.

Neurodevelopmental Disorder in Children Affected by Ocular Albinism Type 1
A Novel X-linked Mutation of CACNA1F Gene in Two Male Siblings Presenting Nystagmus

Monge, S. Gonzalez

Prevalence of Elementary Visuo-spatial Perception Deficit in Children with Neurodevelopmental Disorders

Morandi, A.

Neurodevelopmental Disorder in Children Affected by Ocular Albinism Type 1

Naboni, C.

Developmental Profile of an Italian Cohort of ELBW Preterm Infants Born in the 2000s: Is Emerging Language a Weak Point in Early Development?

Nardocci, N.

Repetitive and Stereotyped Behaviors in Neurodevelopmental Disorders: More than a Movement Disorder

Orcesi, S.

Developmental Profile of an Italian Cohort of ELBW Preterm Infants Born in the 2000s: Is Emerging Language a Weak Point in Early Development?
The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Parazzini, Cecilia

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Pasini, N.

Neurodevelopmental Disorder in Children Affected by Ocular Albinism Type 1

Perotti, G.

Developmental Profile of an Italian Cohort of ELBW Preterm Infants Born in the 2000s: Is Emerging Language a Weak Point in Early Development?

Pichiecchio, Anna

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Pinelli, L.

Neurodevelopmental Disorder in Children Affected by Ocular Albinism Type 1
A Novel X-linked Mutation of CACNA1F Gene in Two Male Siblings Presenting Nystagmus

Pinelli, Lorenzo

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Pisella, L.

Prevalence of Elementary Visuo-spatial Perception Deficit in Children with Neurodevelopmental Disorders

Pisoni, C.

Developmental Profile of an Italian Cohort of ELBW Preterm Infants Born in the 2000s: Is Emerging Language a Weak Point in Early Development?

Plecko, B.

A Case of Vitamin-B6-Dependent Disorder Presenting with Abnormal Eye–Head Movements and Infantile Spasms without Hypsarrhythmia

Ranza, E.

Encephalopathy with Epilepsy and Movement Disorder Related to RNF13: Case Report
Hearing Loss Is Not an Obligatory Hallmark of SPATA5 Early-Onset Epileptic Encephalopathy with Microcephaly and Hypomyelination

Ravelli, C.

Monogenic Chorea Etiologies in Children: A Study of a Cohort of 85 Patients and a Proposal of a Diagnostic Algorithm

Rodrigues, M. T. C. A.

Hearing Loss Is Not an Obligatory Hallmark of SPATA5 Early-Onset Epileptic Encephalopathy with Microcephaly and Hypomyelination

Rodriguez, D.

Monogenic Chorea Etiologies in Children: A Study of a Cohort of 85 Patients and a Proposal of a Diagnostic Algorithm

Roncarolo, F.

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Rossi, A.

Repetitive and Stereotyped Behaviors in Neurodevelopmental Disorders: More than a Movement Disorder
Neurodevelopmental Disorder in Children Affected by Ocular Albinism Type 1

Roubertie, A.

Monogenic Chorea Etiologies in Children: A Study of a Cohort of 85 Patients and a Proposal of a Diagnostic Algorithm

Roulet-Perez, E.

Structural Brain Abnormalities in Epilepsy with Myoclonic Atonic Seizures

Santoni, F.

Encephalopathy with Epilepsy and Movement Disorder Related to RNF13: Case Report

Savoldi, G.

A Novel X-linked Mutation of CACNA1F Gene in Two Male Siblings Presenting Nystagmus

Stronati, M.

Developmental Profile of an Italian Cohort of ELBW Preterm Infants Born in the 2000s: Is Emerging Language a Weak Point in Early Development?

Tesic, I.

A Novel X-linked Mutation of CACNA1F Gene in Two Male Siblings Presenting Nystagmus

Tonduti, D.

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Tritto, G.

Developmental Profile of an Italian Cohort of ELBW Preterm Infants Born in the 2000s: Is Emerging Language a Weak Point in Early Development?

Tzialla, C.

Developmental Profile of an Italian Cohort of ELBW Preterm Infants Born in the 2000s: Is Emerging Language a Weak Point in Early Development?

Van Grambezen, B.

The Neonatal Presentation of BRAT1-Related Neonatal Rigidity and Multifocal Seizure Syndrome

Varesio, C.

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Vega, L.

The Neonatal Presentation of BRAT1-Related Neonatal Rigidity and Multifocal Seizure Syndrome

Veggiotti, P.

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Viri, M.

The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation

Vuillerot, C.

Prevalence of Elementary Visuo-spatial Perception Deficit in Children with Neurodevelopmental Disorders

Yubero, D.

Pharmacological Combination of Sodium Channel Blockers (Oxcarbazepine and Lacosamide) to Control Seizures in Two Patients with Neonatal-Onset Epilepsy due to De Novo SCNA2 Heterozygous Mutation