Abstracts (HTML) List of Authors

Panagiotakaki, E.

Epilepsy in Inv Dup (15) Syndrome: Clnical and Electrophysiological Features in a Case Series of Four Patients
Epilepsy and EEG Patterns in Children Diagnosed with Hyperinsulinism. Report of Two Cases Presented as Atypical Generalized Epilepsy and Review of EEGS of 15 Supplementary Cases.

Pant, D.C.

A Novel Hypomyelinating Leukodystrophy Caused by Loss of the Sphingolipid Desaturase DEGS1 with Potential Therapy

Papadopoulou, M.

Epilepsy in Inv Dup (15) Syndrome: Clnical and Electrophysiological Features in a Case Series of Four Patients

Parazzini, C.

Acute Flaccid Myelitis: An Emerging Disease with Several Challenges. A Retrospective Study of an Italian Cohort.
Proposal of a New Diagnostic Score for Aicardi–Goutières Syndrome

Parker, S.

Design, Baseline Characteristics, and 2-Year Follow-up from The MPS IIIA Natural History Study Used as Control Group in Gene Therapy Trial

Pavlova, M.A.

Social Cognition in Children Autism Spectrum Disorders: An Eye Tracking Study

Pédespan, J.M.

Early-Onset Epileptic Encephalopathy Related to Germline PIGA Mutations: A Series of Four Patients

Pichiecchio, A.

Proposal of a New Diagnostic Score for Aicardi–Goutières Syndrome

Pons, L.

Epilepsy in Inv Dup (15) Syndrome: Clnical and Electrophysiological Features in a Case Series of Four Patients

Prior, T.W.

AVXS-101 Phase 1 Gene-Replacement Therapy (GRT) Clinical Trial in Spinal Muscular Atrophy Type 1 (SMA1): 24-Month Event-Free Survival and Achievement of Developmental Milestones

Pujol, A.

A Novel Hypomyelinating Leukodystrophy Caused by Loss of the Sphingolipid Desaturase DEGS1 with Potential Therapy