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Publications by Pasquale Striano

Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome

American Journal of Human Genetics

English

A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy

American Journal of Human Genetics

English

Biallelic Mutations in ADPRHL2 , Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome

American Journal of Human Genetics

English

TBC1D24, an ARF6-Interacting Protein, Is Mutated in Familial Infantile Myoclonic Epilepsy

American Journal of Human Genetics

English

Correction To: The Landscape of Epilepsy-Related GATOR1 Variants

Genetics in Medicine

English

Contribution of Ultrarare Variants in mTOR Pathway Genes to Sporadic Focal Epilepsies

Annals of Clinical and Translational Neurology

English

NovelGABRG2mutations Cause Familial Febrile Seizures

Neurology: Genetics

English

Whole-Exome Sequencing to Disentangle the Complex Genetics of Hippocampal Sclerosis–temporal Lobe Epilepsy

Neurology: Genetics

English

“Comorbidity” Between Epilepsy and Headache/Migraine: The Other Side of the Same Coin!

Journal of Headache and Pain

English

Gut Microbiota and Psychogenic Non-Epileptic Seizures: I Can Feel It in the Belly

Expert Review of Neurotherapeutics

English