Bernardo Bernardina-Dalla

Verona, Italy

Last Updated: 09/26/2026

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Found 43 publications

Introducing the D-DAND scale: Development of a comprehensive caregiver-administered tool for Dravet syndrome comorbidities.

Introducing the D-DAND scale: Development of a comprehensive caregiver-administered tool for Dravet syndrome comorbidities.

Journal: Epilepsia
Published: February 06, 2026

Electrographic-only seizures and status epilepticus in neonates with Tuberous Sclerosis Complex.

Electrographic-only seizures and status epilepticus in neonates with Tuberous Sclerosis Complex.

Journal: Pediatric research
Published: January 18, 2026

Associations of Cortical and Subcortical White Matter Morphometric Abnormalities With Clinical and Genetic Findings in STXBP1 Encephalopathy.

Associations of Cortical and Subcortical White Matter Morphometric Abnormalities With Clinical and Genetic Findings in STXBP1 Encephalopathy.

Journal: Neurology. Genetics
Published: October 01, 2025

Seizures influence sleep macrostructure and the sleep-wake circadian rhythm in Dravet syndrome.

Seizures influence sleep macrostructure and the sleep-wake circadian rhythm in Dravet syndrome.

Journal: Epilepsia
Published: January 15, 2025

Clinical Reasoning: Hyperventilation-Induced Alternating Hemiplegia With Concomitant Hemispheric EEG Slowing in a 7-Year-Old Girl With Headache.

Clinical Reasoning: Hyperventilation-Induced Alternating Hemiplegia With Concomitant Hemispheric EEG Slowing in a 7-Year-Old Girl With Headache.

Journal: Neurology
Published: August 13, 2024

PRRT2 benign familial infantile seizures (BFIS) with atypical evolution to encephalopathy related to status epilepticus during sleep (ESES).

PRRT2 benign familial infantile seizures (BFIS) with atypical evolution to encephalopathy related to status epilepticus during sleep (ESES).

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: January 16, 2023

Clinical characteristics of 80 subjects with KCNQ2-related encephalopathy: Results from a family-driven survey.

Clinical characteristics of 80 subjects with KCNQ2-related encephalopathy: Results from a family-driven survey.

Journal: Epilepsy & behavior : E&B
Published: September 26, 2022

A registry for Dravet syndrome: The Italian experience.

A registry for Dravet syndrome: The Italian experience.

Journal: Epilepsia open
Published: August 15, 2022

Gelastic seizures and "smiling spasms": A peculiar ictal pattern.

Gelastic seizures and "smiling spasms": A peculiar ictal pattern.

Journal: Epileptic disorders : international epilepsy journal with videotape
Published: April 18, 2022

Adaptive behaviour in adolescents and adults with Dravet syndrome.

Adaptive behaviour in adolescents and adults with Dravet syndrome.

Journal: Developmental medicine and child neurology
Published: March 29, 2022

Epilepsy features in ARID1B-related Coffin-Siris syndrome.

Epilepsy features in ARID1B-related Coffin-Siris syndrome.

Journal: Epileptic disorders : international epilepsy journal with videotape
Published: November 03, 2021

Ictal Electroencephalographic Characteristics of Nodding Syndrome: A Comparative Case-Series from South Sudan, Tanzania, and Uganda.

Ictal Electroencephalographic Characteristics of Nodding Syndrome: A Comparative Case-Series from South Sudan, Tanzania, and Uganda.

Journal: Annals of neurology
Published: July 07, 2021
Showing 1-12 of 43

Last Updated: 09/26/2026