Results 211 to 220 of about 353,121 (342)
Abstract Objective The present study provides normative data for adapted versions of the Rey Auditory Verbal Learning Test (RAVLT) and the Logical Memory subtest from the Wechsler Memory Scales – 3rd edition (WMS‐III‐LM), involving both recall and recognition procedures after a 2‐week delay to assess accelerated long‐term forgetting (ALF).
Amélie Landry +4 more
wiley +1 more source
Orthodontic Treatment Needs in Children with Autism Spectrum Disorder. [PDF]
Prynda M +10 more
europepmc +1 more source
Epilepsy syndromes classification
Abstract Epilepsy syndromes are distinct electroclinical entities which have been recently defined by the International League Against Epilepsy Nosology and Definitions Task Force. Each syndrome is associated with “a characteristic cluster of clinical and EEG features, often supported by specific etiologic findings”.
Elaine C. Wirrell +4 more
wiley +1 more source
Abstract We report two cases of dual genetic diagnoses involving Lafora disease (LD) and co‐occurring neurodevelopmental disorders caused by pathogenic variants in TRIO and SHANK3, respectively. LD is an ultra‐rare, autosomal recessive, severe form of progressive myoclonus epilepsy affecting previously healthy children or adolescents. In both patients,
Lorenzo Muccioli +29 more
wiley +1 more source
A Longitudinal Transdisciplinary Approach for Autism Spectrum Disorder. [PDF]
Kabarite A +8 more
europepmc +1 more source
Frontiers in EEG as a tool for the management of pediatric epilepsy: Past, present, and future
Abstract Electroencephalography (EEG) has evolved into an indispensable tool in pediatric epilepsy, fundamentally transforming the diagnosis, classification, and management of this condition. This review chronicles the historical journey of EEG from its groundbreaking inception to its current pivotal role in delineating distinct pediatric epilepsy ...
Hiroki Nariai
wiley +1 more source
Prematurity and genetic liability for autism spectrum disorder. [PDF]
Zhang Y +4 more
europepmc +1 more source
Abstract Objective To assess the burden of Dravet syndrome (DS) and Lennox–Gastaut syndrome (LGS), including managing seizure and nonseizure symptoms, on patients and caregivers. Methods Data were drawn from the Adelphi Real World DS and LGS Disease Specific Programme™, a cross‐sectional survey in Asia (China, Japan), Europe (France, Germany, Italy ...
Drishti Shah +8 more
wiley +1 more source
Autism Spectrum Disorder: The Cerebellum, Genes, and Pathways. [PDF]
D'Mello SR.
europepmc +1 more source

