Giuditta Pellino

High CSSI-24 scores in paediatric headache suggest a functional disorder and call for a neurodevelopmental biopsychosocial framework: A prospective cohort study.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: November 16, 2025

Pediatric acute-onset neuropsychiatric syndrome and pediatric autoimmune neuropsychiatric disorder associated with streptococcal infections: a delphi study and consensus document about definition, diagnostic criteria, treatment and follow-up.

Journal: Frontiers in immunology

Published: April 20, 2024

Answer to: Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy (Amadori E et al., 2022). EJMG-D-22-00384.

Journal: European journal of medical genetics

Published: September 11, 2022

Pediatric recurrent acute necrotizing encephalomyelitis, RANBP2 genotype and Sars-CoV-2 infection: Diagnosis, pathogenesis and targeted treatments from a case study.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: September 09, 2022

Brivaracetam add-on treatment in pediatric patients with severe drug-resistant epilepsy: Italian real-world evidence.

Journal: Seizure

Published: January 12, 2022

Acute lymphoblastic leukemia in a child with Weiss-Kruszka syndrome: Casual or causal association?

Journal: European journal of medical genetics

Published: September 18, 2021

Operational diagnosis of epilepsy in children at undetermined risk: A meta-analysis of prognostic factors for seizure recurrence.

Journal: Epilepsy & behavior : E&B

Published: August 23, 2021

Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy.

Journal: European journal of medical genetics

Published: August 04, 2021

Early vagus nerve stimulator implantation as a main predictor of positive outcome in pediatric patients with epileptic encephalopathy.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: June 29, 2021

Mitofusin 2: The missing link between mtDNA maintenance defects and neurotransmitter disorders.

Journal: Mitochondrion

Published: April 02, 2021

Epilepsy in isolated parenchymal neurocutaneous melanosis: A systematic review.

Journal: Epilepsy & behavior : E&B

Published: February 16, 2020

Prognostic factors in epileptic encephalopathies at onset in the first 2 years of life: The experience of a tertiary healthcare center in Italy.

Journal: Epilepsy & behavior : E&B

Published: April 15, 2019

High CSSI-24 scores in paediatric headache suggest a functional disorder and call for a neurodevelopmental biopsychosocial framework: A prospective cohort study.

High CSSI-24 scores in paediatric headache suggest a functional disorder and call for a neurodevelopmental biopsychosocial framework: A prospective cohort study.

Pediatric acute-onset neuropsychiatric syndrome and pediatric autoimmune neuropsychiatric disorder associated with streptococcal infections: a delphi study and consensus document about definition, diagnostic criteria, treatment and follow-up.

Pediatric acute-onset neuropsychiatric syndrome and pediatric autoimmune neuropsychiatric disorder associated with streptococcal infections: a delphi study and consensus document about definition, diagnostic criteria, treatment and follow-up.

Answer to: Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy (Amadori E et al., 2022). EJMG-D-22-00384.

Answer to: Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy (Amadori E et al., 2022). EJMG-D-22-00384.

Pediatric recurrent acute necrotizing encephalomyelitis, RANBP2 genotype and Sars-CoV-2 infection: Diagnosis, pathogenesis and targeted treatments from a case study.

Pediatric recurrent acute necrotizing encephalomyelitis, RANBP2 genotype and Sars-CoV-2 infection: Diagnosis, pathogenesis and targeted treatments from a case study.

Brivaracetam add-on treatment in pediatric patients with severe drug-resistant epilepsy: Italian real-world evidence.

Brivaracetam add-on treatment in pediatric patients with severe drug-resistant epilepsy: Italian real-world evidence.

Acute lymphoblastic leukemia in a child with Weiss-Kruszka syndrome: Casual or causal association?

Acute lymphoblastic leukemia in a child with Weiss-Kruszka syndrome: Casual or causal association?

Operational diagnosis of epilepsy in children at undetermined risk: A meta-analysis of prognostic factors for seizure recurrence.

Operational diagnosis of epilepsy in children at undetermined risk: A meta-analysis of prognostic factors for seizure recurrence.

Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy.

Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy.

Early vagus nerve stimulator implantation as a main predictor of positive outcome in pediatric patients with epileptic encephalopathy.

Early vagus nerve stimulator implantation as a main predictor of positive outcome in pediatric patients with epileptic encephalopathy.

Mitofusin 2: The missing link between mtDNA maintenance defects and neurotransmitter disorders.

Mitofusin 2: The missing link between mtDNA maintenance defects and neurotransmitter disorders.

Epilepsy in isolated parenchymal neurocutaneous melanosis: A systematic review.

Epilepsy in isolated parenchymal neurocutaneous melanosis: A systematic review.

Prognostic factors in epileptic encephalopathies at onset in the first 2 years of life: The experience of a tertiary healthcare center in Italy.

Prognostic factors in epileptic encephalopathies at onset in the first 2 years of life: The experience of a tertiary healthcare center in Italy.

Prognostic factors in epileptic encephalopathies at onset in the first 2 years of life: The experience of a tertiary healthcare center in Italy.

Prognostic factors in epileptic encephalopathies at onset in the first 2 years of life: The experience of a tertiary healthcare center in Italy.