Cannabidiol in patients with seizures associated with Lennox-Gastaut syndrome (GWPCARE4): a randomised, double-blind, placebo-controlled phase 3 trial
Summary Background Patients with Lennox-Gastaut syndrome, a rare, severe form of
epileptic encephalopathy, are frequently treatment resistant to available medications. No …
epileptic encephalopathy, are frequently treatment resistant to available medications. No …
Learning and thinking styles: An analysis of their interrelationship and influence on academic achievement
F Cano-Garcia, EH Hughes - Educational psychology, 2000 - Taylor & Francis
This study examined whether college students' learning styles (LS) and thinking styles (TS)
were interrelated, and if these could predict academic achievement. A total of 210 college …
were interrelated, and if these could predict academic achievement. A total of 210 college …
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
Idiopathic focal epilepsy (IFE) with rolandic spikes is the most common childhood epilepsy,
comprising a phenotypic spectrum from rolandic epilepsy (also benign epilepsy with …
comprising a phenotypic spectrum from rolandic epilepsy (also benign epilepsy with …
Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous …
Objective To report the clinical and investigative features of children with a clinical diagnosis
of probable autoimmune encephalopathy, both with and without antibodies to central …
of probable autoimmune encephalopathy, both with and without antibodies to central …
Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum
A McTague, R Appleton, S Avula, JH Cross, MD King… - Brain, 2013 - academic.oup.com
Migrating partial seizures of infancy, also known as epilepsy of infancy with migrating focal
seizures, is a rare early infantile epileptic encephalopathy with poor prognosis, presenting …
seizures, is a rare early infantile epileptic encephalopathy with poor prognosis, presenting …
Nurses' perceptions of continuing professional development
E Hughes - Nursing Standard (through 2013), 2005 - search.proquest.com
professional development Page 1 CLINICAL RESEARCH - EDUCATION Nurses’
perceptions of continuing professional development The synthesis of art and science is …
perceptions of continuing professional development The synthesis of art and science is …
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
D Bertrand, F Elmslie, E Hughes, J Trounce… - Neurobiology of …, 2005 - Elsevier
Mutations in nAChRs are found in a rare form of nocturnal frontal lobe epilepsy (ADNFLE).
Previously, some nAChR mutations have been described that are associated with additional …
Previously, some nAChR mutations have been described that are associated with additional …
Fenfluramine in the treatment of Dravet syndrome: results of a third randomized, placebo‐controlled clinical trial
J Sullivan, L Lagae, JH Cross, O Devinsky… - …, 2023 - Wiley Online Library
Objective This study was undertaken to assess the safety and efficacy of fenfluramine in the
treatment of convulsive seizures in patients with Dravet syndrome. Methods This multicenter …
treatment of convulsive seizures in patients with Dravet syndrome. Methods This multicenter …
[HTML][HTML] Incorporating epilepsy genetics into clinical practice: a 360 evaluation
S Oates, S Tang, R Rosch, R Lear, EF Hughes… - NPJ genomic …, 2018 - nature.com
We evaluated a new epilepsy genetic diagnostic and counseling service covering a UK
population of 3.5 million. We calculated diagnostic yield, estimated clinical impact, and …
population of 3.5 million. We calculated diagnostic yield, estimated clinical impact, and …
Clinical spectrum of STX1B-related epileptic disorders
Objective The aim of this study was to expand the spectrum of epilepsy syndromes related to
STX1B, encoding the presynaptic protein syntaxin-1B, and establish genotype-phenotype …
STX1B, encoding the presynaptic protein syntaxin-1B, and establish genotype-phenotype …