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  1. 11121
    “…CONCLUSION: The findings illustrate that Naglieri Nonverbal Ability Test is a valid and reliable intelligence test for measuring general intellectual ability and for assessing reasoning skills.…”
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    Norm and Standardization Study for Naglieri Nonverbal Ability Test, 5-9 Age Group
  2. 11122
    “…Finally, we report damaging variants in CDK16 and TRPC5 in patients with intellectual disability or autism spectrum disorders. …”
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    Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X
  3. 11123
    “…A total of 55.84% (129/231) of the children with ASD had an intellectual disability. Only 46.32% (107/231) started receiving intervention within 1 month after diagnosis. …”
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    The intervention dilemma and high burden of children with autism in Guizhou province, Southwest China
  4. 11124
    “…The results will also guide the design of a mixed method research study to examine the extent of trauma symptomatology and potentially traumatising experiences, and how they relate to the mental health of caregivers of adults with intellectual and developmental disability from different cultural backgrounds.…”
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    Protocol for scoping review study to map out the existing research in relation to post-traumatic stress symptoms among caregivers of individuals with neurodevelopmental, psychiatric and neurocognitive disorders
  5. 11125
    “…BACKGROUND: School nutrition programs impact the intellectual, social, and emotional development of school children, as well as their future risk of developing Non-Communicable Diseases. …”
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    Toward the upscaling of school nutrition programs in Dubai: An exploratory study
  6. 11126
    “…Prenatal exposure to the anti-seizure medication sodium valproate (VPA) is associated with an increased risk of adverse postnatal neurodevelopmental outcomes, including lowered intellectual ability, autism spectrum disorder and attention-deficit hyperactivity disorder. …”
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    Integrative genomics reveals pathogenic mediator of valproate-induced neurodevelopmental disability
  7. 11127
    “…For the subset (n = 314, 79.1%) with 22q11.2 deletion extent, we used a binomial logistic regression model to predict short stature in 22q11.2DS, accounting for effects of sex, age, ancestry, major congenital heart disease (CHD), moderate-to-severe intellectual disability (ID), and 22q11.2 deletion extent. …”
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    Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome
  8. 11128
    “…OBJECTIVE: We aimed to determine the genetic cause of syndromic POI, intellectual disability, neutropenia, and cataracts. …”
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    Premature Ovarian Insufficiency in CLPB Deficiency: Transcriptomic, Proteomic and Phenotypic Insights
  9. 11129
    “…BACKGROUND: Fragile X syndrome (FXS) is the most prevalent form of inherited intellectual disability and is commonly associated with autism. …”
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    Neural response to repeated auditory stimuli and its association with early language ability in male children with Fragile X syndrome
  10. 11130
    “…Intellectual disability with or without manifestations of autism and/or epilepsy affects 1–2% of the population, and it is estimated that more than 30–50% of these cases have a single genetic cause. …”
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    GenIDA: an international participatory database to gain knowledge on health issues related to genetic forms of neurodevelopmental disorders
  11. 11131
    “…The legal and ethical ramifications of feeding patients’ facial images to a neural network for diagnostic purposes are related to patient consent, data privacy, data security, liability, and intellectual property. Current ethico-legal regulation practices seem incapable of addressing all concerns and ensuring accountability. …”
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    Artificial intelligence in medico-dental diagnostics of the face: a narrative review of opportunities and challenges
  12. 11132
    “…BACKGROUND: Hao-fountain syndrome (HAFOUS) is a neurodevelopmental syndrome characterized by global developmental and severe language delays, behavioral abnormalities (including autism), and mild dysmorphic impairment of intellectual development. It is a dominant genetic disease caused by USP7 gene (*602519) mutations on chromosome 16p13.2. …”
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    Expansion of the mutation spectrum and phenotype of USP7-related neurodevelopmental disorder
  13. 11133
    “…FXS is one of the leading monogenic causes of intellectual disability (ID) and autism. Although it is caused by the failure of a single gene, FMRP that functions as an RNA binding protein affects a large number of genes secondarily. …”
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    The inhibition of NCS-1 binding to Ric8a rescues fragile X syndrome mice model phenotypes
  14. 11134
    por Botha, Monique, Cage, Eilidh
    Publicado 2022
    “…Instrumentality (a form of objectification) was key to whether researchers considered a person to have social value with emphasis revolving around intellectual ability and independence. Lastly, language seemed to act as a tool of normalization of violence. …”
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    “Autism research is in crisis”: A mixed method study of researcher’s constructions of autistic people and autism research
  15. 11135
    “…Core deficits in short-term and working memory, visuospatial constructional ability, verbal fluency, and fine motor skills underlie distorted intellectual and academic achievement. This study aimed to assess the individual differences in cognitive ability and fine motor skills of pediatric tumor survivors and the age-matched healthy controls. …”
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    Comparison of Neurocognitive Functioning and Fine Motor Skills in Pediatric Cancer Survivors and Healthy Children
  16. 11136
    “…Patients with a pathogenic de novo mutation in one of these genes, in part, present with overlapping features, such as generalized hypotonia, intellectual and developmental delay, facial dysmorphologies, seizures, and autistic features, and, in part, with opposite features, e.g., smaller versus larger head sizes or normal versus absent corpus callosum. …”
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    Clinical and molecular characteristics of a novel rare de novo variant in PPP2CA in a patient with a developmental disorder, autism, and epilepsy
  17. 11137
    “…An 18-year-old male patient with a history of status epilepticus and severe intellectual disability was transferred to our hospital for a thorough examination of fever and constipation that had lasted for 2 months. …”
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    A case of pheochromocytoma associated with liver abscess and intestinal pseudo-obstruction
  18. 11138
    “…Child's ASD severity, intellectual and socio-adaptive skills and parent's socio-demographic characteristics were collected from ELENA follow-up. …”
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    Anxiety and depression in parents of children with autism spectrum disorder during the first COVID-19 lockdown: Report from the ELENA cohort
  19. 11139
    “…Subjects with DS show a large heterogeneity of phenotypes and the most constant clinical features present are typical facies and intellectual disability (ID). Several studies demonstrated that trisomy 21 causes an alteration in the metabolic profile, involving among all the one-carbon cycle. …”
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    One-carbon pathway metabolites are altered in the plasma of subjects with Down syndrome: Relation to chromosomal dosage
  20. 11140
    “…Focus groups were conducted for each of six disability sub-groups: vision, hearing, mobility and physical, mental health, cognitive, intellectual, and developmental, and chronic illness. …”
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    New obstacles and widening gaps: A qualitative study of the effects of the COVID-19 pandemic on U.S. adults with disabilities
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