Author response: SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy
- 25 February 2020
- journal article
- letter
- Published by Ovid Technologies (Wolters Kluwer Health) in Neurology
- Vol. 94 (8), 370
- https://doi.org/10.1212/WNL.0000000000009010
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
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- A synaptic protein defect associated with reflex seizure disorderNeurology, 2019
- Chewing induced reflex seizures (“eating epilepsy”) and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 casesSeizure, 2018
- Eyelid myoclonia with absences (Jeavons syndrome): A well‐defined idiopathic generalized epilepsy syndrome or a spectrum of photosensitive conditions?Epilepsia, 2009
- Early‐ and Late‐onset Complications of the Ketogenic Diet for Intractable EpilepsyEpilepsia, 2004