1 |
Screen time in 36-month-olds at increased likelihood for ASD and ADHD.
|
|
|
|
BASE
|
|
Show details
|
|
2 |
Screen time in 36-month-olds at increased likelihood for ASD and ADHD.
|
|
|
|
BASE
|
|
Show details
|
|
3 |
Protocol for a transdiagnostic study of children with problems of attention, learning and memory (CALM). ...
|
|
|
|
BASE
|
|
Show details
|
|
4 |
Protocol for a transdiagnostic study of children with problems of attention, learning and memory (CALM).
|
|
|
|
BASE
|
|
Show details
|
|
5 |
A Pilot Study of the Efficacy of a Cognitive Training Based on Board Games in Children with Attention-Deficit/Hyperactivity Disorder: A Randomized Controlled Trial
|
|
|
|
BASE
|
|
Show details
|
|
6 |
Screening and diagnosis of learning disabilities/disorders - outcomes of interdisciplinary assessments
|
|
|
|
In: Revista CEFAC, Vol 21, Iss 5 (2019) (2019)
|
|
BASE
|
|
Show details
|
|
7 |
Predictors of bullying and victimisation in children with attention-deficit/hyperactivity disorder ... : Napovedovalci ustrahovanja in viktimizacije otrok z motnjo pozornosti s hiperaktivnostjo ...
|
|
|
|
BASE
|
|
Show details
|
|
8 |
Predictors of bullying and victimisation in children with attention-deficit/hyperactivity disorder ; Napovedovalci ustrahovanja in viktimizacije otrok z motnjo pozornosti s hiperaktivnostjo
|
|
|
|
In: CEPS Journal 8 (2018) 4, S. 63-88 (2018)
|
|
BASE
|
|
Show details
|
|
9 |
Kognitive Profile bei lese-rechtschreibschwachen Kindern mit und ohne Aufmerksamkeitsprobleme
|
|
|
|
In: Lernen und Lernstörungen 6 (2017) 4, S. 169-181 (2017)
|
|
BASE
|
|
Show details
|
|
10 |
Developmental Dyslexia and/or co-occurring Attention Deficit: Investigation of prevalence, underlying cognitive deficits, and family risk in a self-selected sample of parents and children ...
|
|
|
|
BASE
|
|
Show details
|
|
11 |
Kognitive Profile bei lese-rechtschreibschwachen Kindern mit und ohne Aufmerksamkeitsprobleme ...
|
|
|
|
BASE
|
|
Show details
|
|
12 |
Developmental Dyslexia and/or co-occurring Attention Deficit: Investigation of prevalence, underlying cognitive deficits, and family risk in a self-selected sample of parents and children
|
|
|
|
BASE
|
|
Show details
|
|
13 |
CATALISE: a multinational and multidisciplinary Delphi consensus study. Identifying language impairments in children
|
|
|
|
BASE
|
|
Show details
|
|
14 |
Observation of children with attention-deficit hyperactivity (ADHD) problems in three natural classroom contexts
|
|
|
|
In: British Journal of Educational Psychology (2015)
|
|
BASE
|
|
Show details
|
|
15 |
Observation of children with attention-deficit hyperactivity (ADHD) problems in three natural classroom contexts
|
|
|
|
In: British Journal of Educational Psychology (2015)
|
|
BASE
|
|
Show details
|
|
16 |
Language problems in children with ADHD: a community-based study
|
|
|
|
BASE
|
|
Show details
|
|
17 |
Akademisches Selbstkonzept im Grundschulalter. Entwicklungsanalyse dimensionaler Vergleiche und Exploration differenzieller Unterschiede
|
|
|
|
In: 2014, 98 S. - (Zugl.: Frankfurt am Main, Univ., Diss., 2012) (2014)
|
|
BASE
|
|
Show details
|
|
18 |
A comparison of working memory profiles in school-aged children with Specific Language Impairment, Attention Deficit/Hyperactivity Disorder, Comorbid SLI and ADHD and their typically developing peers
|
|
|
|
BASE
|
|
Show details
|
|
19 |
Congenital perisylvian dysfunction - is it a spectrum?
|
|
|
|
In: Dev Med Child Neurol , 52 (1) pp. 33-39. (2010) (2010)
|
|
Abstract:
AIM: This study examines the overlap between children with bulbar cerebral palsy (Worster-Drought syndrome [WDS]) and perisylvian polymicrogyria. METHOD: A total of 121 children (81 males, 40 females; mean age 5y 5mo, SD 3y 6mo; age range 1mo-15y 4mo) were studied using retrospective clinical data and magnetic resonance imaging. In all, 70 children had WDS with normal perisylvian imaging, 31 had congenital bilateral perisylvian polymicrogyria (CBPP), and 20 had congenital unilateral perisylvian polymicrogyria (CUPP). RESULTS: All groups shared aetiological markers (male sex, congenital contractures, low familial incidence, excess antenatal events). There was a common phenotype of pseudobulbar palsy with mild limb pyramidal signs in all children with WDS, 90% of those with CBPP, and one-third of those with CUPP, often also associated with learning disability*, epilepsy, and behavioural difficulties. A further 15% of children with CUPP acquired this phenotype through an epileptic encephalopathy. Pseudobulbar palsy rather than polymicrogyria was more predictive of additional impairments other than epilepsy. INTERPRETATION: We propose that congenital perisylvian dysfunction is a spectrum encompassing the WDS phenotype and perisylvian polymicrogyria imaging abnormalities. As with other prenatal brain abnormalities, there is not necessarily concordance between imaging and clinical findings, although the phenotype is often more severe to manifest imaging abnormality. Clinical phenotype is the best indicator of prognosis. Epileptic encephalopathy can cause an acquired form of perisylvian dysfunction where there is.
|
|
Keyword:
Adolescent; Attention Deficit Disorder with Hyperactivity; Cerebral; Cerebral Cortex; Cerebral Palsy; Child; Child Development Disorders; Comorbidity; Consanguinity; Diagnosis; Differential; Dominance; Epilepsy; Female; Great Britain; Humans; Infant; Language Development Disorders; Magnetic Resonance Imaging; Male; Malformations of Cortical Development; Pervasive; Phenotype; Preschool; Retrospective Studies; Speech Disorders; Syndrome
|
|
URL: http://discovery.ucl.ac.uk/1383877/
|
|
BASE
|
|
Hide details
|
|
20 |
Auditory processing disorder in relation to developmental disorders of language, communication and attention: a review and critique.
|
|
|
|
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2009)
|
|
BASE
|
|
Show details
|
|
|
|