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  1. 11581
    “…Those with a diagnosis of intellectual disability or a neurological disorder known to affect cognition were excluded. …”
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    Ultrarare Coding Variants and Cognitive Function in Schizophrenia
  2. 11582
    “…Neurodevelopmental morbidity included cerebral palsy, epilepsy, intellectual disability, autism spectrum disorder, sensorineural defects, and minor neurodevelopmental disorders. …”
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    Endogenous erythropoietin at birth is associated with neurodevelopmental morbidity in early childhood
  3. 11583
    por Kiese-Himmel, Christiane
    Publicado 2022
    “…However, according to this conceptualization, only children with an intellectual disability (IQ < 70) would be excluded from the diagnosis. …”
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    Früherkennung primärer Sprachentwicklungsstörungen – zunehmende Relevanz durch Änderung der Diagnosekriterien?
  4. 11584
    “…Chromosomal microarray analysis (CMA) has been recommended and practiced routinely since 2010 both in the USA and Europe as the first-tier cytogenetic test for patients with unexplained neurodevelopmental delay/intellectual disability, autism spectrum disorders, and/or multiple congenital anomalies. …”
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    Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil
  5. 11585
    “…LAY ABSTRACT: In sub-Saharan Africa, there are few services for children with developmental disabilities such as autism and intellectual disability. One way to support these children is to include them in mainstream schools. …”
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    Stakeholder experiences, attitudes and perspectives on inclusive education for children with developmental disabilities in sub-Saharan Africa: A systematic review of qualitative studies
  6. 11586
    “…The three aims of the current study were as follows: (i) to examine the psychosocial status among patients with genetically confirmed FH, (ii) to compare their intellectual capacity and cognitive outcomes with a reference group, and (iii) to examine the relationship between health literacy and cognitive functioning. …”
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    A Comprehensive Neuropsychological Study of Familial Hypercholesterolemia and Its Relationship with Psychosocial Functioning: A Biopsychosocial Approach
  7. 11587
    “…RESULTS: The 4 patients displayed mild-to-severe intellectual developmental disorder, which was accompanied by speech delay, dysmorphic facies, and serious caries. …”
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    Identification of two novel variants of the BCL11B gene in two Chinese pedigrees associated with neurodevelopmental disorders
  8. 11588
    “…It is often characterized, especially in males, by intellectual disability, anxiety, repetitive behavior, social communication deficits, delayed language development, and abnormal sensory processing. …”
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    Baclofen-associated neurophysiologic target engagement across species in fragile X syndrome
  9. 11589
    “…To demonstrate the plausibility of the approach, we investigated the effect of a PHF8 F279S clinical mutation associated with X-linked intellectual disability, which has been experimentally shown to ablate PHF8-catalyzed demethylation. …”
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    Can Second Coordination Sphere and Long-Range Interactions Modulate Hydrogen Atom Transfer in a Non-Heme Fe(II)-Dependent Histone Demethylase?
  10. 11590
    por Zvereva, N., Zvereva, M.
    Publicado 2021
    “…Pearson correlation coefficient between STQ-77, BRAQ and Gaps DR-CAT found in normal group: Gap DR-CAT “Health” – STQ-77 “Physical Endurance” (r=-.508, p<0.05), Gap DR-CAT “Smart” - STQ-77 “Intellectual Endurance” (r=-.521, P<0.05), Gap DR-CAT “Happiness” – BRAQ “Hostility” (r=.528, p<0.05), Gap DR-CAT “Happiness” - STQ-77 “Impulsivity” (r=.432, p<0.05), “Neuroticism” (r=.539,p<0.01). …”
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    Features of interconnection between temperament, self-esteem and aggressiveness in adolescents with mental and somatic pathology
  11. 11591
    “…Globally, approximately 50% of people with cerebral palsy have an intellectual disability and there is significant risk for domain-specific cognitive impairments for the majority of people with cerebral palsy. …”
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    A validation and acceptability study of cognitive testing using switch and eye-gaze control technologies for children with motor and speech impairments: A protocol paper
  12. 11592
    “…Patient 1 exhibited a unique constellation of clinical features including marked hydrocephalus, spondyloepimetaphyseal dysplasia (SEMD), and thrombocytopenia which is comparable to that of an infant reported by Faye-Peterson et al., whereas patients 2 and 3 showed Camera-Genevieve type SMED with intellectual/developmental disability which is currently known as the sole disease name for NANS-CDG. …”
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    Clinical and molecular findings in three Japanese patients with N-acetylneuraminic acid synthetase-congenital disorder of glycosylation (NANS-CDG)
  13. 11593
    “…Users engaged in a wide variety of discussion topics with their Replika, including intellectual topics, life and work, recreation, mental health, connection, Replika, current events, and other people. …”
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    Assessing the Topics and Motivating Factors Behind Human-Social Chatbot Interactions: Thematic Analysis of User Experiences
  14. 11594
    “…Although the prevalence of severe problems identified by both approaches was similar, comprehensive medical examinations could detect overlooked problems such as severe pulmonary dysfunction, dental maldevelopment, and borderline intellectual functioning, which might have an impact on quality of life in CCSs.…”
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    Significance of active screening for detection of health problems in childhood cancer survivors
  15. 11595
    “…RESULTS: BN models showed associations between early motor items and developmental coordination disorders, borderline intelligence/intellectual disability, and speech and language disorder. …”
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    How Accurately Does the Information on Motor Development Collected During Health Checkups for Infants Predict the Diagnosis of Neurodevelopmental Disorders? – A Bayesian Network Model-Based Study
  16. 11596
    “…Patients affected by complex I deficiency harboring homozygous NUBPL variants typically have neurological problems including seizures, intellectual disability, and ataxia associated with cerebellar hypoplasia. …”
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    Early embryonic lethality in complex I associated p.L104P Nubpl mutant mice
  17. 11597
    “…BACKGROUND AND OBJECTIVES: Fragile X syndrome (FXS) is a neurodevelopmental disorder, identified as the most common cause of hereditary intellectual disability and monogenic cause of autism spectrum disorders (ASDs), caused by the loss of fragile X mental retardation protein (FMRP). …”
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    Increased Serum Levels of miR-125b and miR-132 in Fragile X Syndrome: A Preliminary Study
  18. 11598
    “…Genetic variants in Ankyrin Repeat Domain 11 (ANKRD11) and deletions in 16q24.3 are known to cause KBG syndrome, a rare syndrome associated with craniofacial, intellectual, and neurobehavioral anomalies. We report 25 unpublished individuals from 22 families with molecularly confirmed diagnoses. …”
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    KBG syndrome: videoconferencing and use of artificial intelligence driven facial phenotyping in 25 new patients
  19. 11599
    “…Cardiomyopathy was the most prevalent finding (22; 63.2%), followed by developmental delay/intellectual disability (15; 39.5%), long QT (14; 36.8%), seizures (12; 31.6%), failure to thrive (4; 10.5%), and basal ganglia strokes (3; 7.9%). …”
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    Natural history of propionic acidemia in the Amish population
  20. 11600
    “…Results: At admission to LTACH, 42.2% of PMV patients were in a vegetative state/ minimally conscious state (VS/MCS); 32.5% were severely cognitively impaired, 11.0% were mildly to moderately cognitively impaired, 12.3% had no cognitive impairment, and 1.9% had intellectual disability/psychiatric disorder. In-LTACH LOS (months) decreased from 34.6 ± 42.6 at age 40–59y, 19.1 ± 22.3 at 60–79y to 14.4 ± 19.3 at age ≥80y (p = .006). …”
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    Prognosis of Chronically Ventilated Patients in a Long-Term Ventilation Facility: Association with Age, Consciousness and Cognitive State
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