Results 121 to 130 of about 5,090,991 (269)

Attention-deficit/hyperactivity disorder: a systems perspective. A comprehensive qualitative analysis of the literature [PDF]

open access: yes, 2001
Plan BAttention-Deficit/Hyperactivity Disorder (ADHD) is a neurological syndrome resulting in problems with self-regulation. ADHD is characterized by inattention and/or hyperactivity-impulsivity which causes impairment in at least two settings.
Reali, Ann T.
core  

Food Addiction and Psychiatric Comorbidity: A Latent Profile Analysis

open access: yesInternational Journal of Eating Disorders, EarlyView.
ABSTRACT Objective Food addiction (FA) frequently co‐occurs with eating disorders (EDs), PTSD, mood/anxiety disorders, and substance use disorders (SUDs), yet few studies have examined clinically meaningful subgroups in multi‐morbid treatment populations.
Dean Bilenker   +3 more
wiley   +1 more source

Systematic Review of Psychotherapy for Adult Attention Deficit Hyperactivity Disorder [poster] [PDF]

open access: yes
This article aims to systematically assess the quality of primary research studies using cognitive behavioral therapy and alternative therapies as primary and/or adjunctive treatment for adult attention deficit hyperactivity disorder, investigate the ...
Gonzalez, Alissa
core   +1 more source

A study of an animal model of Attention-Deficit/ Hyperactivity Disorder using in vivo chronoamperometry and behavioural responses to methylphenidate and guanfacine [PDF]

open access: yes, 2010
Includes abstract.~Includes bibliographical references (leaves 119-147).Attention-Deficit/Hyperactivity Disorder (ADHD) is a childhood disorder that is behaviorally characterized by developmentally inappropriate levels of inattention, impulsivity and ...
Hsin-Wen Hsieh, Jennifer
core  

Dietary patterns in children with epilepsy: The role of household environment and clinical comorbidities

open access: yesEpileptic Disorders, EarlyView.
Abstract Objective To evaluate dietary patterns in children with epilepsy and compare them with age‐ and sex‐matched healthy siblings living in the same household environment. Associations between clinical characteristics and dietary adequacy were also examined.
Ana Claudia Cândido Oliveira   +5 more
wiley   +1 more source

KBG syndrome: A scoping review of electroclinical features of patients with epilepsy

open access: yesEpileptic Disorders, EarlyView.
Abstract Background and Objectives KBG syndrome is a rare autosomal developmental disorder caused by pathogenic variants of the ANKRD11 gene. This scoping review aimed to explore all current literature data regarding clinical and electroencephalographic features of patients with KBG syndrome and epilepsy. Materials and Methods We conducted a literature
Stefania Kalampokini   +6 more
wiley   +1 more source

Attention deficit hyperactivity disorder (ADHD) within a South Indian (Keralian) mainstream school context [PDF]

open access: yes
Attention Deficit Hyperactivity Disorder (ADHD) is a widely discussed special educational issue in Western contexts and developed countries. By contrast, limited information is available about ADHD in Eastern contexts and developing countries.
Jament, Johnson
core  

Oligogenic inheritance in epilepsy: A systematic exome‐wide analysis

open access: yesEpilepsia, EarlyView.
Abstract Objective Genetic factors contribute to the majority of epilepsies, but the exact genetic cause remains unknown in most patients. Incomplete penetrance and variable expressivity are frequent, and recent studies showed a burden of deleterious variants in epilepsy genes, suggesting a role for oligogenic inheritance.
Sarah Duerinckx   +192 more
wiley   +1 more source

Symptomatic improvement in fibromyalgia after treatment of comorbid attention deficit hyperactivity disorder: a case report

open access: yesJournal of Medical Case Reports
Background Attention deficit hyperactivity disorder is a common disorder that has an association with fibromyalgia. The connection between the two is incompletely understood but may be due to specific neurotransmitter abnormalities.
Josephine Chiu   +3 more
doaj   +1 more source

Functional profiling of STXBP1 missense variants using a novel dual‐readout fluorometric assay

open access: yesEpilepsia, EarlyView.
Abstract Objective STXBP1‐related disorders (STXBP1‐RD) are among the most common genetic neurodevelopmental disorders, marked by early onset epilepsy, global developmental delay, and motor impairments. Many missense variants remain uncharacterized, limiting accurate variant interpretation and hindering development of precision therapies.
Elisa A. Waxman   +11 more
wiley   +1 more source

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