Salvatore Striano

Naples, Italy

Last Updated: 09/26/2026

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Found 78 publications

Faciobrachial dystonic seizures: Epileptic events or paroxysmal motor network disorder?

Faciobrachial dystonic seizures: Epileptic events or paroxysmal motor network disorder?

Journal: Epilepsia

Published: March 16, 2026

Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing.

Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing.

Journal: Epilepsia

Published: July 12, 2023

Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbidities.

Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbidities.

Journal: Epilepsia

Published: December 01, 2022

Epilepsy in "Sunflower syndrome": electroclinical features, therapeutic response, and long-term follow-up.

Epilepsy in "Sunflower syndrome": electroclinical features, therapeutic response, and long-term follow-up.

Journal: Seizure

Published: June 10, 2021

Temporal-parietal-occipital epilepsy in GEFS+ associated with SCN1A mutation.

Temporal-parietal-occipital epilepsy in GEFS+ associated with SCN1A mutation.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: April 14, 2021

Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy.

Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy.

Journal: Neurology

Published: December 21, 2020

Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlations.

Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlations.

Journal: Journal of the neurological sciences

Published: December 08, 2020

Diagnosis and Management of Type 1 Sialidosis: Clinical Insights from Long-Term Care of Four Unrelated Patients.

Diagnosis and Management of Type 1 Sialidosis: Clinical Insights from Long-Term Care of Four Unrelated Patients.

Journal: Brain sciences

Published: June 25, 2020

Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene.

Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: June 21, 2020

Epilepsy, cerebral calcifications, and gluten-related disorders: Are anti-transglutaminase 6 antibodies the missing link?

Epilepsy, cerebral calcifications, and gluten-related disorders: Are anti-transglutaminase 6 antibodies the missing link?

Journal: Seizure

Published: September 13, 2019

Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study.

Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study.

Journal: Epilepsy & behavior : E&B

Published: July 15, 2019

Clinical evolution and epilepsy outcome in three patients with CDKL5-related developmental encephalopathy.

Clinical evolution and epilepsy outcome in three patients with CDKL5-related developmental encephalopathy.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: June 22, 2019

Showing 1-12 of 78

Last Updated: 09/26/2026