[HTML][HTML] Cannabinoids: therapeutic use in clinical practice

C Pagano, G Navarra, L Coppola, G Avilia…�- International journal of�…, 2022 - mdpi.com
Medical case reports suggest that cannabinoids extracted from Cannabis sativa have
therapeutic effects; however, the therapeutic employment is limited due to the psychotropic�…

Seizures and epilepsy: an overview for neuroscientists

CE Stafstrom, L Carmant�- Cold Spring�…, 2015 - perspectivesinmedicine.cshlp.org
Epilepsy is one of the most common and disabling neurologic conditions, yet we have an
incomplete understanding of the detailed pathophysiology and, thus, treatment rationale for�…

Antisense oligonucleotides increase Scn1a expression and reduce seizures and SUDEP incidence in a mouse model of Dravet syndrome

Z Han, C Chen, A Christiansen, S Ji, Q Lin…�- Science translational�…, 2020 - science.org
Dravet syndrome (DS) is an intractable developmental and epileptic encephalopathy
caused largely by de novo variants in the SCN1A gene, resulting in haploinsufficiency of the�…

Fenfluramine for treatment-resistant seizures in patients with Dravet syndrome receiving stiripentol-inclusive regimens: a randomized clinical trial

R Nabbout, A Mistry, S Zuberi, N Villeneuve…�- JAMA�…, 2020 - jamanetwork.com
Importance Fenfluramine treatment may reduce monthly convulsive seizure frequency in
patients with Dravet syndrome who have poor seizure control with their current stiripentol�…

The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications

A Brunklaus, T Br�nger, T Feng, C Fons, A Lehikoinen…�- Brain, 2022 - academic.oup.com
Brain voltage-gated sodium channel NaV1. 1 (SCN1A) loss-of-function variants cause the
severe epilepsy Dravet syndrome, as well as milder phenotypes associated with genetic�…

The core Dravet syndrome phenotype

C Dravet�- Epilepsia, 2011 - Wiley Online Library
Dravet syndrome was described in 1978 by Dravet (1978) under the name of severe
myoclonic epilepsy in infancy (SMEI). The characteristics of the syndrome were confirmed�…

Developmental and epileptic encephalopathies: what we do and do not know

N Specchio, P Curatolo�- Brain, 2021 - academic.oup.com
Developmental encephalopathies, including intellectual disability and autistic spectrum
disorder, are frequently associated with infant epilepsy. Epileptic encephalopathy is used to�…

[BOOK][B] Developmental neuropsychology: A clinical approach

V Anderson, E Northam, J Wrennall - 2018 - taylorfrancis.com
This fully updated edition of Developmental Neuropsychology: A Clinical Approach
addresses key issues in child neuropsychology with a unique emphasis on evidence�…

[HTML][HTML] Use of cannabidiol in the treatment of epilepsy: efficacy and security in clinical trials

S Silvestro, S Mammana, E Cavalli, P Bramanti…�- Molecules, 2019 - mdpi.com
Cannabidiol (CBD) is one of the cannabinoids with non-psychotropic action, extracted from
Cannabis sativa. CBD is a terpenophenol and it has received a great scientific interest�…

Sudden unexpected death in epilepsy: current knowledge and future directions

T Tomson, L Nashef, P Ryvlin�- The Lancet Neurology, 2008 - thelancet.com
Although largely neglected in earlier literature, sudden unexpected death in epilepsy
(SUDEP) is the most important epilepsy-related mode of death, and is the leading cause of�…