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  1. 2061
    “…Adults with intellectual disabilities (ID) often live a sedentary lifestyle and have higher rates of overweight and obesity. …”
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    Design and methods of a multi-component physical activity program for adults with intellectual disabilities living in group homes
  2. 2062
    “…Increased intragenic DNA methylation of the Fragile X Related Epigenetic Element 2 (FREE2) in blood has been correlated with lower intellectual functioning in females with fragile X syndrome (FXS). …”
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    Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X
  3. 2063
    “…In recent years, people with intellectual and developmental disabilities (IDD) have moved from institutionalized settings to local community residences. …”
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    Evaluating the Impact of a Clinician Improvement Program for Treating Patients with Intellectual and Developmental Disabilities: The Challenging Case of Mississippi
  4. 2064
    “…Defects in neuronal migration cause brain malformations, which are associated with intellectual disability (ID) and epilepsy. Using exome sequencing, we identified compound heterozygous variants (p.Arg71His and p. …”
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    Identification of a novel synaptic protein, TMTC3, involved in periventricular nodular heterotopia with intellectual disability and epilepsy
  5. 2065
    “…Intellectual disability (ID) affects up to 2% of the population world-wide and often coincides with other neurological conditions such as autism spectrum disorders. …”
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    Altered Gene-Regulatory Function of KDM5C by a Novel Mutation Associated With Autism and Intellectual Disability
  6. 2066
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    Publisher Correction: Impaired oxidative stress response characterizes HUWE1-promoted X-linked intellectual disability
  7. 2067
    “…Previously, we have associated a homozygous variant in EDC3 with autosomal recessive intellectual disability. Here, we investigate the functional role of EDC3. …”
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    Integrative bioinformatics analysis characterizing the role of EDC3 in mRNA decay and its association to intellectual disability
  8. 2068
    “…Several truncation mutations, microdeletions and missense variants have been identified and result in a recognizable phenotypic profile, including microcephaly, intellectual disability, epileptic seizures, autism spectrum disorder and language delay. …”
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    Functional characterization of DYRK1A missense variants associated with a syndromic form of intellectual deficiency and autism
  9. 2069
    “…Intellectual disability affects 2–3% of the world's population and typically begins during childhood, causing impairments in social skills and cognitive abilities. …”
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    Pharmacological Modulation of AMPAR Rescues Intellectual Disability-Like Phenotype in Tm4sf2(−/y) Mice
  10. 2070
    “…Persons with intellectual disability (ID) and associated multiple disabilities have been found by many researchers to be a population with deficient physical fitness measures, which can be explained by an inactive lifestyle, a result of lack of awareness of the positive physical effects of physical exercise, or lack of motivation for any motor activity. …”
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    Physical Fitness and Functional Ability of Children with Intellectual Disability: Effects of a Short-Term Daily Treadmill Intervention
  11. 2071
    “…BACKGROUND: Intellectual disability (ID) is the most prevalent disability in the world. …”
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    Intellectual disability rights and inclusive citizenship in South Africa: What can a scoping review tell us?
  12. 2072
    “…X-linked intellectual disability (XLID) is a heterogeneous syndrome affecting mainly males. …”
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    RNF12 X-Linked Intellectual Disability Mutations Disrupt E3 Ligase Activity and Neural Differentiation
  13. 2073
    “…CONCLUSION: The common features among patients are developmental delay, speech delay, mild to moderate intellectual disability and unspecific dysmorphic features. …”
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    Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability
  14. 2074
    “…We reviewed the literature and performed in silico analysis to determine the association between mutations and intellectual disability in patients with CIPA. We found that intellectual disability was correlated with the specific Ntrk1 protein domain that a mutation jeopardized. …”
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    Phenotypic heterogeneity of intellectual disability in patients with congenital insensitivity to pain with anhidrosis: A case report and literature review
  15. 2075
    por Miyazaki, Kei
    Publicado 2018
    “…It is a serious intellectual COI that the Chair of the SPRINT trial steering committee was commissioned as chair of the guideline panel. …”
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    Overdiagnosis or not? 2017 ACC/AHA high blood pressure clinical practice guideline: Consequences of intellectual conflict of interest
  16. 2076
    “…CASE REPORT: Here, we report the case of a patient with a novel homozygous truncating mutation in KCNMA1 (p.Arg458Ter) presenting with both the loss- and gain-of-function phenotype with paroxysmal dyskinesia, epilepsy, intellectual delay, and corticospinal–cerebellar tract atrophy. …”
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    Expanding the Phenotype of Homozygous KCNMA1 Mutations; Dyskinesia, Epilepsy, Intellectual Disability, Cerebellar and Corticospinal Tract Atrophy
  17. 2077
    “…BACKGROUND: Data regarding lacosamide treatment as an adjunctive therapy in patients representative of a focal-onset epilepsy population including those with and without intellectual/developmental disorders (IDDs) are limited. …”
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    Adjunctive lacosamide treatment for adult focal-onset epilepsy: focus on comorbid intellectual/developmental disorders and differing responses
  18. 2078
    “…BACKGROUND: Older adults with intellectual disability have high rates of lifestyle-related illness yet remain poorly engaged in physical activity and nutrition interventions. …”
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    ‘Get Healthy!’ A physical activity and nutrition program for older adults with intellectual disability: pilot study protocol
  19. 2079
    “…INTRODUCTION: Exome sequencing is recognized as a powerful tool for identifying the genetic cause of intellectual disability (ID). It is uncertain, however, whether only the exome of the proband should be sequenced or if the sequencing of parental genomes is also required, and the resulting increase in diagnostic yield justifies the increase in costs. …”
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    Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases
  20. 2080
    por Van Norman, Gail A., Eisenkot, Roï
    Publicado 2017
    “…Part 1 reviews basic aspects of intellectual property rights, primarily patents and copyrights. …”
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    Technology Transfer: From the Research Bench to Commercialization: Part 1: Intellectual Property Rights—Basics of Patents and Copyrights
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