lucio giordano

Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia

Italy

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Articles (8)

Year:

2025

Year:

2024

Year:

2023

Year:

2023

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Collaborators (4)

Gaetano Cantalupo

Associate Professor

University of Verona

ITALY

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Ivan Ivanovski

University of Zurich

SWITZERLAND

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Anna Rosati

University of Florence

ITALY

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Davide Mei

Dirigente Professioni Sanitarie Tecnico Diagnostiche

ITALY

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lucio giordano

Research Interests

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Articles (8)

UBA5‐epileptic encephalopathy: new patient, a novel variant, and a review of epileptic phenotypes

Are SCN2A‐related BFNISs also responsible for seizures in adulthood? A case report opens new scenarios

A PUS7 gene pathogenic variant causing self‐injurious behavior, sleep disturbances, and developmental delay: A case report

WISC‐IV intellectual profiles in Italian children with self‐limited epilepsy with centrotemporal spikes

Expanding the genetic and phenotypic spectrum of CHD2‐related disease: From early neurodevelopmental disorders to adult‐onset epilepsy

Cognitive, Behavioral, and Sensory Profile of Pallister–Killian Syndrome: A Prospective Study of 22 Individuals

Further delineation and long-term evolution of electroclinical phenotype in Mowat Wilson Syndrome. A longitudinal study in 40 individuals

Cerebral folate transporter deficiency syndrome in three siblings: Why genetic testing for developmental and epileptic encephalopathies should be performed early and include the FOLR1 gene

Collaborators (4)

Gaetano Cantalupo

Ivan Ivanovski

Anna Rosati

Davide Mei

Make your next move.

lucio giordano

Research Interests

Explore related searches

Contact this professor

Articles (8)

UBA5‐epileptic encephalopathy: new patient, a novel variant, and a review of epileptic phenotypes

Are SCN2A‐related BFNISs also responsible for seizures in adulthood? A case report opens new scenarios

A PUS7 gene pathogenic variant causing self‐injurious behavior, sleep disturbances, and developmental delay: A case report

WISC‐IV intellectual profiles in Italian children with self‐limited epilepsy with centrotemporal spikes

Expanding the genetic and phenotypic spectrum of CHD2‐related disease: From early neurodevelopmental disorders to adult‐onset epilepsy

Cognitive, Behavioral, and Sensory Profile of Pallister&ndash;Killian Syndrome: A Prospective Study of 22 Individuals

Further delineation and long-term evolution of electroclinical phenotype in Mowat Wilson Syndrome. A longitudinal study in 40 individuals

Cerebral folate transporter deficiency syndrome in three siblings: Why genetic testing for developmental and epileptic encephalopathies should be performed early and include the FOLR1 gene

Collaborators (4)

Gaetano Cantalupo

Ivan Ivanovski

Anna Rosati

Davide Mei

Make your next move.

Cognitive, Behavioral, and Sensory Profile of Pallister–Killian Syndrome: A Prospective Study of 22 Individuals