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A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment
autism intellectual disability
2015/12/18
FOXP1 (forkhead box protein P1; OMIM 605515) belongs to the FOX
gene family of transcription factor proteins, defined by the presence of
a characteristic DNA-binding domain known as the forkhe...
Psychopathology in Adults with Autism and Intellectual Disability
Autism intellectual disability psychiatric co-morbidity
2015/7/31
There have been few studies of psychopathology in adult with autism. This study examined psychiatric co-morbidity in 147 adults with intellectual disability (ID) and autism and 605 adults with ID but ...
Traumatic experiences and life events in people with intellectual disability
intellectual disability life events mental health psychopathology traumatic experiences,
2015/7/29
The aim of this article is to present and critically evaluate recent research on life events and traumatic experiences as predictors of psychopathology in people with intellectual disability.
A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment
FOXP1 variant autism intellectual disability severe speech language impairment
2015/5/13
FOXP1 (forkhead box protein P1) is a transcription factor involved in the development of several tissues, including the brain. An emerging phenotype of patients with protein-disrupting FOXP1 variants ...
Differences in Physical Activity among Youth with and without Intellectual Disability
ACCELEROMETER CHILDREN ADOLESCENT SEX SPORT PARTICIPATION ANTHROPOMETRY
2017/4/14
Introduction: Very little is known about physical activity (PA) and PA patterns measured with objective methods among children with intellectual disability (ID).
Purpose: This study aimed to investig...
The discovery of 139 Child Non-syndromic Intellectual Disability associated genetic copy number variation loci with biological insights
Gene copy biological
2014/12/5
Intellectual disability (ID) is a highly heritable mental disease. Especially, the
underlying molecular mechanism of non-syndromic intellectual disability (NSID), a
subtype of ID with no ...
Investigation of Genetic Causes of Intellectual Disability in Kerman Province,South East of Iran
Intellectual disability Microcephaly Iran
2015/9/25
Background: Intellectual disability (ID) has a worldwide prevalence of 1-3% and results from extraordinary heterogeneous. To shed more light on the causes of ID in Kerman Province, in Southeast Iran, ...
Level of selected fitness abilities of pupils at practical elementary schools in relation to the aetiology of their intellectual disability
Intellectual disability aetiology of intellectual disability practical elementary schools fitness abilities
2009/12/25
The objective of the study was to determine the level of the selected fitness abilities of 153 pupils (aged 10.62 ± 0.56 years) at practical elementary schools in Prague in relation to the aetiology o...