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  1. 11041
    “…Dominant GNAO1 mutations cause an emerging group of childhood-onset neurological disorders characterized by developmental delay, intellectual disability, movement disorders, drug-resistant seizures and neurological deterioration. …”
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    Caenorhabditis elegans provides an efficient drug screening platform for GNAO1-related disorders and highlights the potential role of caffeine in controlling dyskinesia
  2. 11042
    “…Precise machining of such materials requires inputs of intellectual machining approaches, such as wire electrical discharge machining (WEDM). …”
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    Multi-Response Optimization of Al(2)O(3) Nanopowder-Mixed Wire Electrical Discharge Machining Process Parameters of Nitinol Shape Memory Alloy
  3. 11043
    “…In the association analysis, intellectual disability was widely associated with all target regions. …”
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    Abnormal White Matter Microstructure in the Limbic System Is Associated With Tuberous Sclerosis Complex-Associated Neuropsychiatric Disorders
  4. 11044
    “…Neuronal migration defects are considered a critical etiology of neurodevelopmental disorders, including autism spectrum disorders (ASDs), schizophrenia, epilepsy, and intellectual disability (ID). TRIO is a high-risk candidate gene for ASDs and ID. …”
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    RhoGEF Trio Regulates Radial Migration of Projection Neurons via Its Distinct Domains
  5. 11045
    “…There are wide range of behaviors associated with these mutations, including intellectual disabilities, changes in temperament, and autism. …”
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    CTCF in parvalbumin-expressing neurons regulates motor, anxiety and social behavior and neuronal identity
  6. 11046
    “…In particular, one CNV was identified in a subset of children clinically diagnosed with intellectual disabilities (ID) that results in a hemizygous deletion of multiple genes at chromosome 16p12.1. …”
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    16p12.1 Deletion Orthologs are Expressed in Motile Neural Crest Cells and are Important for Regulating Craniofacial Development in Xenopus laevis
  7. 11047
    “…AUTS2 syndrome is a genetic disorder that causes intellectual disability, microcephaly, and other phenotypes. …”
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    AUTS2 Syndrome: Molecular Mechanisms and Model Systems
  8. 11048
    “…The atmosphere of constant scrutiny of academic ability that prevails in medical colleges may leave some students at risk of expressing feelings of intellectual fraudulence and phoniness. Impostor phenomenon (IP) traits have been associated with anxiety, depression, job dissatisfaction, and poor professional performance. …”
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    Impostor Phenomenon and Its Relationship to Self-Esteem Among Students at an International Medical College in the Middle East: A Cross Sectional Study
  9. 11049
    “…Professionals in healthcare services for people with intellectual disabilities in four residential settings in Sweden are included in the educational-intervention based on web-based training and structured group reflections. …”
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    Studying intraprofessional and interprofessional learning processes initiated by an educational intervention applying a qualitative design with multimethod approach: a study protocol
  10. 11050
    “…Loss-of-function variants in PHD Finger Protein 8 (PHF8) cause Siderius X-linked intellectual disability (ID) syndrome, hereafter called PHF8-XLID. …”
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    Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
  11. 11051
    “…Persons with mental health issues or intellectual disabilities, especially those living in residential settings, are especially vulnerable to SBV because they often receive long-term intimate care. …”
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    Combining rules and dialogue: exploring stakeholder perspectives on preventing sexual boundary violations in mental health and disability care organizations
  12. 11052
    “…BACKGROUND AND OBJECTIVES: To report on the novel association of biallelic variant in atonal basic helix-loop-helix transcription factor 1 (ATOH1) gene and pontocerebellar hypoplasia (PCH), severe global developmental delay, intellectual disability, and hearing loss in a family with 2 affected siblings. …”
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    Biallelic ATOH1 Gene Variant in Siblings With Pontocerebellar Hypoplasia, Developmental Delay, and Hearing Loss
  13. 11053
    “…Autism spectrum disorder (ASD) and intellectual disability (ID) often exist together in patients. …”
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    Clinical characterization of a novel RAB39B nonstop mutation in a family with ASD and severe ID causing RAB39B downregulation and study of a Rab39b knock down mouse model
  14. 11054
    “…We also identified UT moderators that contemporary and future medical educators may be able to harness in order to develop learner UT as a healthcare graduate attribute, especially through teaching practices such as intellectual candor. Further research is now required to evaluate the impact of proposed educational interventions, and to develop effective assessments of students' skills for managing clinical uncertainties.…”
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    Medical Student Experiences of Uncertainty Tolerance Moderators: A Longitudinal Qualitative Study
  15. 11055
    “…The presence of abnormalities concerning X chromosome can also contribute to many genetically heterogeneous diseases associated with cognitive impairment and intellectual disability. PURPOSE: This study shows the effect of aberrations of the maternal X chromosome on the abnormal development of the child. …”
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    Clinical Importance of aCGH in Genetic Counselling of Children with Psychomotor Retardation
  16. 11056
    “…Subcortical heterotopias are malformations associated with epilepsy and intellectual disability, characterized by the presence of ectopic neurons in the white matter. …”
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    Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development
  17. 11057
    “…Children with WBS share a distinct neurobehavioral phenotype including mild to severe intellectual disability, severely impaired visual spatial abilities, relatively preserved verbal expressive skills, anxiety problems, enhanced social motivation (i.e., hypersociable behaviors) and socio-communicative problems. …”
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    A Comparison of Adaptive Functioning Between Children With Duplication 7 Syndrome and Williams-Beuren Syndrome: A Pilot Investigation
  18. 11058
    “…Importantly, most SEBD are “invisible,” so these parents and children may face more stigma, have less support, and fewer inclusive programming opportunities than are typically available for children with physical or intellectual disabilities. Children’s challenging behavioral characteristics are not visibly attributable to a medical or physical condition, and thus are not often viewed empathetically, and cannot easily be managed in the context of programming. …”
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    Presenting a New Framework to Improve Engagement in Physical Activity Programs for Children and Adolescents With Social, Emotional, and Behavioral Disabilities
  19. 11059
    “…We evaluated late cognitive effects in children treated with a high-dose cytarabine based regimen, focusing on general intellectual ability and specific neurocognitive domains. …”
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    Neurocognitive deficits in survivors of childhood acute myeloid leukemia
  20. 11060
    Publicado 2022
    “…The child at age of 3 years was now brought to our OPD with mild delay in all domains of development with an intellectual level of 2 and half years at the age of 3 years. …”
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    Abstract- Poster: ANCIPS 2022: Abstract for Poster Presentation: E- Poster: Titlex: Autism in a child with Pierre Robin Sequence: A Case Report
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