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  1. 10081
    “…DESIGN AND METHODS: Young people with CP aged 14–18 years without severe intellectual impairment were identified from regional registers of CP in Northern Ireland and the North of England. χ(2) and Mann-Whitney U tests were used to assess differences in CP and sociodemographic characteristics between those recruited and those who refused. …”
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    Did previous involvement in research affect recruitment of young people with cerebral palsy to a longitudinal study of transitional health care?
  2. 10082
    “…INTRODUCTION: intellectual capacity measured as intelligence quotient (IQ) is one of the determinants of school performance of children. …”
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    Academic performance and intelligence quotient of primary school children in Enugu
  3. 10083
    “…DOORS [deafness, onychodystrophy, osteodystrophy, intellectual disability (mental retardation), and seizures] syndrome can be caused by mutations in the TBC1D24 and ATP6V1B2 genes, both of which are involved in endolysosomal function. …”
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    Clinicopathological Relationships in an Aged Case of DOORS Syndrome With a p.Arg506X Mutation in the ATP6V1B2 Gene
  4. 10084
    “…The quality of the studies varied widely and there was a lack of studies from low- and middle-income countries and for certain types of mental disorders (e.g. intellectual disabilities and eating disorders). Our study showed that certain groups of mental disorders are more costly than others and that these rankings are relatively stable between countries. …”
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    The cost of mental disorders: a systematic review
  5. 10085
    “…Exclusion criteria included substance use, psychosis, and severe intellectual disability. Forty‐two patients were assessed for eligibility and 32 were randomized. …”
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    Retraining and control therapy for pediatric psychogenic non‐epileptic seizures
  6. 10086
    “…METHODS: a cross-sectional study conducted among 226 randomly selected children living with physical disabilities; learning, intellectual and developmental disabilities; deafness, blindness and hearing impairment disabilities aged between 7 and 20 years old, who live and/or are under the care of NYANZA Home de la Vierge des Pauvres (HVP) GATAGARA. …”
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    Prevalence of dental caries and associated risk factors in children living with disabilities in Rwanda: a cross-sectional study
  7. 10087
    “…Variants were more commonly identified in patients with a developmental delay or intellectual disability (DD/ID), but genetic status was not associated with the severity of DD/ID. …”
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    Clinical and genetic characteristics of patients with Doose syndrome
  8. 10088
    “…However, this potential will be curtailed if C-19 legislation is inadequately operationalised and/or prioritises physical health to the detriment of children’s intellectual, emotional, social and security needs. To overcome such risks, social ecologies must work with legislators to co-design and co-operationalise C-19 legislation that will not only protect children, but advance their resilience.…”
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    Child protection and resilience in the face of COVID-19 in South Africa: A rapid review of C-19 legislation
  9. 10089
    “…One male case with autism spectrum disorder carried a novel splice-site mutation and a female case with intellectual disability carried an intragenic tandem duplication. …”
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    Presynaptic dysfunction in CASK-related neurodevelopmental disorders
  10. 10090
    “…Situatively, these skills are often used in combination and challenge students on an intellectual, communicative and emotional level. Conclusion: The ability to (self-)reflect should be more strongly integrated in university medical training by providing appropriate support, especially since it presents students with specific challenges to (self-)reflexively approach their own future as doctors. …”
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    (Self-)Reflexion and training of professional skills in the context of “being a doctor” in the future – a qualitative analysis of medical students' experience in LET ME ... keep you real!
  11. 10091
    “…METHODS: We applied trio‐ and single‐whole exome sequencing to search for genetic sequence variants associated with a wide range of epileptic phenotypes accompanied by intellectual disability and/or global developmental delay in the investigated patients. …”
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    Rare variants in the GABA(A) receptor subunit ε identified in patients with a wide spectrum of epileptic phenotypes
  12. 10092
    “…AIMS: To produce a revised formula for estimating local need for secondary mental health, learning disability (intellectual disability) and psychological therapies services for adults in England. …”
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    Estimating local need for mental healthcare to inform fair resource allocation in the NHS in England: cross-sectional analysis of national administrative data linked at person level
  13. 10093
    “…She presented with dysmorphic features, hypo/hyper pigmentation of the skin, intellectual disability and craniosynostosis. G-banding chromosome analysis suggested mos 46,XX,psu idic(18)(p11.2)[25]/46,XX,r(?…”
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    Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report
  14. 10094
    “…Mutations in the gene encoding the ubiquitously expressed RNA-binding protein ZC3H14 result in a non-syndromic form of autosomal recessive intellectual disability in humans. Studies in Drosophila have defined roles for the ZC3H14 ortholog, Nab2 (aka Drosophila Nab2 or dNab2), in axon guidance and memory due in part to interaction with a second RNA-binding protein, the fly Fragile X homolog Fmr1, and coregulation of shared Nab2-Fmr1 target mRNAs. …”
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    A Genetic Screen Links the Disease-Associated Nab2 RNA-Binding Protein to the Planar Cell Polarity Pathway in Drosophila melanogaster
  15. 10095
    “…Primary data collected over a six-month period from expert professionals with five years’ (or more) experience in pediatric, intellectual disability and/or palliative care settings. …”
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    Integration of palliative care in services for children with life-limiting neurodevelopmental disabilities and their families: a Delphi study
  16. 10096
    “…CONTEXT: Prader-Willi syndrome (PWS) is a complex hypothalamic disorder, combining hyperphagia, hypotonia, intellectual disability, and pituitary hormone deficiencies. …”
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    Missed Diagnoses and Health Problems in Adults With Prader-Willi Syndrome: Recommendations for Screening and Treatment
  17. 10097
    “…Cataract, limited eye movement, electrocardiographic abnormalities, intellectual disability, and recurrent miscarriages were observed in some of the affected individuals. …”
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    A large deletion spanning PITX2 and PANCR in a Chinese family with Axenfeld-Rieger syndrome
  18. 10098
    por Son, Kyung-Bok
    Publicado 2020
    “…RESULTS: Similar to the provisions for intellectual property, the scope of international agreements regarding pricing and reimbursement decisions are broadened and strengthened. …”
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    Understanding the trends in international agreements on pricing and reimbursement for newly marketed medicines and their implications for access to medicines: a computational text analysis
  19. 10099
    “…Fragile X syndrome (FXS) is the leading cause of inherited intellectual disability and autism spectrum disorder. …”
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    Response to Placebo in Fragile X Syndrome Clinical Trials: An Initial Analysis
  20. 10100
    “…Results: Most patients had severe autism and severe/moderate intellectual disability. Eleven patients were already in the unit when it was hit by the pandemic, and five were admitted from the community. …”
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    Autism and COVID-19: A Case Series in a Neurodevelopmental Unit
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