Results 151 to 160 of about 689,446 (396)

Attention Deficit Hyperactivity Disorder (ADHD): Forensic Issues

open access: yesBond Law Review
ADHD has long been recognised as disproportionately present in both juvenile and adult prison populations. This is so for a number of reasons, including the potential for persons with ADHD to be disinhibited, impulsive, impaired in executive functioning ...
Ian Freckelton
doaj  

Attention-deficit hyperactivity disorder

open access: yesThe Lancet, 2020
J. Posner, G. Polanczyk, E. Sonuga-Barke
semanticscholar   +1 more source

Cryptic Splicing of GAP43 mRNA is a Novel Hallmark of TDP‐43‐Associated ALS and AD

open access: yesAdvanced Science, EarlyView.
TDP‐43 dysfunction disrupts RNA processing, inducing cryptic exon 4a1 inclusion in GAP43 and reducing its protein levels. This aberrant splicing impairs axonal regeneration and contributes to neurodegeneration in ALS and AD. RNA‐seq of patient brains reveals GAP43 downregulation and 4a1 upregulation, identifying cryptic exon 4a1 as a potential ...
Mingming Yang   +9 more
wiley   +1 more source

Actual treatment of attention deficit hyperactivity disorder (ADHD) [PDF]

open access: yes, 2013
El tratamiento del trastorno por défi cit de atención e hiperactividad (TDAH) incluye intervenciones farmacológicas, psicosociales y educativas, y en él se aconseja un diseño personalizado teniendo en cuenta las características del paciente, el tipo de ...
Martín Calero, María José   +2 more
core  

Attention deficit hyperactivity disorder and elementary teachers awareness

open access: yes, 2013
About 8.7% of children suffer from Attention Deficit Hyperactivity Disorder and 20 to 30% of them have learning disability. Since elementary teacher is the first one who recognize this problem, we aimed at evaluating Teachers Knowledge about Attention ...
Taghi Badeleh, M.
core   +1 more source

Exome Sequencing Reveals the Genetic Architecture of Non‐syndromic Orofacial Clefts and Identifies BOC as a Novel Causal Gene

open access: yesAdvanced Science, EarlyView.
Nonsyndromic orofacial clefts (NSOFCs) are the most common craniofacial defects. Exome sequencing of 214 sporadic cases sheds new light on its genetic architecture and identifies many candidate pathogenic variants. Furthermore, functional studies establish BOC as a novel causal gene and reveal an unusual two‐locus model of inheritance via the epistatic
Qing He   +16 more
wiley   +1 more source

Prevalence of Attention-Deficit/Hyperactivity Disorder: A Systematic Review and Meta-analysis

open access: yesPediatrics, 2015
Rae Thomas   +4 more
semanticscholar   +1 more source

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