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1.
The Association Between Anxiety Symptoms and Sleep in School-Aged Children: A Combined Insight From the Children's Sleep Habits Questionnaire and Actigraphy.
Behav Sleep Med
; 16(2): 169-184, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-27254114
2.
Visual attention and academic performance in children with developmental disabilities and behavioural attention deficits.
Dev Sci
; 20(6)2017 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-27649816
3.
Executive Dysfunction in Female FMR1 Premutation Carriers.
Cerebellum
; 15(5): 565-9, 2016 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-27126308
4.
Computerised attention training for children with intellectual and developmental disabilities: a randomised controlled trial.
J Child Psychol Psychiatry
; 57(12): 1380-1389, 2016 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-27550746
5.
Maternal predictors of anxiety risk in young males with fragile X.
Am J Med Genet B Neuropsychiatr Genet
; 165B(5): 399-409, 2014 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-24832235
6.
Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers.
Am J Med Genet B Neuropsychiatr Genet
; 165B(1): 41-51, 2014 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-24166828
7.
The interplay between executive control and motor functioning in Williams syndrome.
Dev Sci
; 16(3): 428-42, 2013 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-23587040
8.
Selective subcortical contributions to gait impairments in males with the FMR1 premutation.
J Neurol Neurosurg Psychiatry
; 88(2): 188-190, 2017 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-27683920
9.
Selective spatial processing deficits in an at-risk subgroup of the fragile X premutation.
Brain Cogn
; 79(1): 39-44, 2012 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-22417865
10.
Association of the DAT1 genotype with inattentive behavior is mediated by reading ability in a general population sample.
Brain Cogn
; 77(3): 453-8, 2011 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-21889247
11.
Higher Tablet Use Is Associated With Better Sustained Attention Performance but Poorer Sleep Quality in School-Aged Children.
Front Psychol
; 12: 742468, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-35046864
12.
Gamified Attention Training in the Primary School Classroom: A Cluster-Randomized Controlled Trial.
J Atten Disord
; 25(8): 1146-1159, 2021 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-31718386
13.
Mapping self-reports of working memory deficits to executive dysfunction in Fragile X Mental Retardation 1 (FMR1) gene premutation carriers asymptomatic for FXTAS.
Brain Cogn
; 73(3): 236-43, 2010 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-20573435
14.
A child-focused version of the Attention Network Task designed to investigate interactions between the attention networks, including the endogenous orienting network.
Child Neuropsychol
; 26(5): 666-690, 2020 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-31833444
15.
Lifespan changes in working memory in fragile X premutation males.
Brain Cogn
; 69(3): 551-8, 2009 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-19114290
16.
Reduced caudate volume and cognitive slowing in men at risk of fragile X-associated tremor ataxia syndrome.
Brain Imaging Behav
; 13(4): 1128-1134, 2019 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-30046972
17.
Development of static and dynamic perception for luminance-defined and texture-defined information.
Neuroreport
; 19(2): 225-8, 2008 Jan 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-18185113
18.
Age-dependent cognitive changes in carriers of the fragile X syndrome.
Cortex
; 44(6): 628-36, 2008 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-18472033
19.
Impact of the Fragile X mental retardation 1 (FMR1) gene premutation on neuropsychiatric functioning in adult males without fragile X-associated Tremor/Ataxia syndrome: a controlled study.
Am J Med Genet B Neuropsychiatr Genet
; 147B(6): 859-72, 2008 Sep 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-18165971
20.
ß-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies.
PLoS One
; 13(2): e0192151, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29474364