Results 101 to 110 of about 18,911 (261)
What for…A CAE Past‐Presidential Address
ABSTRACT This is a lightly revised (read copy‐edited) rendering of my CAE Past‐President's address, which was presented live on Nov. 10, 2022 at the AAA annual meeting in Seattle.
Edmund ‘Ted’ Hamann
wiley +1 more source
Abstract Objective This study was undertaken to describe incidence and distribution of seizures, etiologies, and epilepsy syndromes in the general child and youth population, using the current International League Against Epilepsy (ILAE) classifications. Methods The study platform is the Norwegian Mother, Father, and Child Cohort Study (MoBa). Epilepsy
Truls Vikin +4 more
wiley +1 more source
Tremor as an intrinsic feature of juvenile myoclonic epilepsy
Abstract We aim to understand whether tremor may be an intrinsic feature of juvenile myoclonic epilepsy (JME) and whether individuals with JME plus tremor experience a different disease course. Thirty‐one individuals with JME plus tremor (17 females, mean age = 33.9 ± 13.8 years) and 30 age of onset‐ and gender‐matched subjects with JME (21 females ...
Alessia Giugno +7 more
wiley +1 more source
Consell de redacció Revista Catalana de Dret Públic
doaj +1 more source
Abstract Objective Photosensitive epilepsy (PSE) is a reflex epilepsy, where abnormal electroencephalographic (EEG) responses are induced by photic stimulation. Photosensitivity is classified into four types based on the propagation of the brain's response to visual stimuli.
Lili Timar +6 more
wiley +1 more source
Abstract Objective Seizure self‐reporting is known to be unreliable, particularly with non‐convulsive seizures. There is increasing interest in long‐term monitoring systems to detect and count seizures, including the use of the minimally‐invasive CE‐marked subcutaneous unilateral electroencephalography (EEG) recording system, which has been shown to ...
Tudor Munteanu +11 more
wiley +1 more source
Clinical and genetic landscape of epilepsies with absence seizures and single‐gene etiology
Abstract Objective To characterize the clinical, electroencephalographic, and genetic features of epilepsies featuring absence seizures within monogenic etiology, highlighting the diagnostic, treatment and prognostic implications. Methods We conducted a retrospective, multicenter study including patients with monogenic epilepsies and ...
Simona Balestrini +50 more
wiley +1 more source
Abstract Objective Conditions presenting with both epilepsy and movement disorders (EPIMDs) range from relatively benign cases to severe developmental encephalopathies. However, the full clinical and genetic spectrum still needs to be better defined.
Davide Caputo +15 more
wiley +1 more source

