M. Budetta

Gelastic epilepsy without hypothalamic hamartoma: Three additional cases

S. Savasta, M. Villa, P. Parisi, 2014, Epilepsy & Behavior.

Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy

P. Striano, F. Zara, R. Biancheri, 2006, Neurology.

Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance

P. Striano, F. Zara, C. Minetti, 2013, Epilepsia.

Nutritional problems in children with neuromotor disabilities: an Italian case series

P. Vajro, G. Coppola, R. D'Aniello, 2014, Italian Journal of Pediatrics.

STXBP1 encephalopathy

P. Striano, K. Sleegers, G. Cantalupo, 2016, Neurology.

Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional Study.

P. Striano, F. Zara, R. Manara, 2023, Pediatric neurology.

Epilepsy Course and Developmental Trajectories in STXBP1-DEE

P. Striano, A. Coppola, G. Cantalupo, 2022, Neurology: Genetics.