Results 221 to 230 of about 172,893 (331)

Autistic Traits as Predictors of Increased Obsessive–Compulsive Disorder Severity: The Role of Inflexibility and Communication Impairment [PDF]

open access: gold
Liliana Dell’Osso   +8 more
openalex   +1 more source

Gut‐microbiota‐brain Axis and post‐traumatic epilepsy

open access: yesEpilepsia Open, EarlyView.
Abstract There has been growing evidence that perturbations in gut‐microbiota‐brain axis (GMBA) are involved in mechanisms of chronic sequelae of traumatic brain injury (TBI). This review discusses the connection between GMBA and post‐traumatic epilepsy (PTE), the latter being a common outcome of TBI.
Andrey Mazarati
wiley   +1 more source

Structured clinical diagnostic assessment reveals autism spectrum disorder in adults with functional neurological disorder. [PDF]

open access: yesSci Rep
Gonzalez-Herrero B   +5 more
europepmc   +1 more source

Mobile Application for Tracking Children with Autistic Spectrum Disorder: Content Validation and Usability

open access: gold
Camila Porpino Maia Garcia   +11 more
openalex   +1 more source

Epilepsy syndromes classification

open access: yesEpilepsia Open, EarlyView.
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

Differentiating autism spectrum disorder and global developmental delay in preschoolers: overlapping profiles and diagnostic challenges. [PDF]

open access: yesFront Psychol
Sperandini V   +7 more
europepmc   +1 more source

The challenge of ultra‐rarity: Dual diagnosis of Lafora disease and developmental encephalopathies linked to TRIO and SHANK3 pathogenic variants

open access: yesEpilepsia Open, EarlyView.
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

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