Results 21 to 30 of about 65,099 (252)
The effects of aging and perceived loneliness on lexical ambiguity resolution
Frontiers in Psychology, 2022 Language is central to the interactional nature of the social life within which it is situated. To react or respond in a particular situation, we must be able to recognize the social situation.
Nannan Zhou +12 more
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Chaucer’s Reworking of the Ovidian 'Locus Amoenus' [PDF]
Limina: A Journal of Historical and Cultural Studies, 2014 The locus amoenus or pleasant place is a literary construct which can be traced back to the writings of Homer. It is an area of repose and relaxation in a natural setting consisting of shady trees, soft grass, cool water and occasionally flowers.
Brid Phillips
doaj
Gaboxadol in Fragile X Syndrome: A 12-Week Randomized, Double-Blind, Parallel-Group, Phase 2a Study
Frontiers in Pharmacology, 2021 Background: Fragile X syndrome (FXS), the most common single-gene cause of intellectual disability and autism spectrum disorder (ASD), is caused by a >200-trinucleotide repeat expansion in the 5’ untranslated region of the fragile X mental retardation
Dejan B. Budimirovic +11 more
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Ovid’s Poems in the Printed Books of Sixteenth- and Seventeenth-Century Hungary
Acta Universitatis Carolinae Philologica, 2020 Masterpieces of the classical Latin poetry were continuously among the products of the printing presses. Although Ovid was among the popular antique authors, researches in the sixteenth- and seventeenth-century history of Hungarian book-printing show a ...
Eszter Kovács
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Journal of Curriculum Theorizing, 2022 Curriculum scholarship provides the engagement with curriculum differentiation that has defined the field since its inception. Mainly, curriculum scholars shift from the role of science as arbiter of truth to the politics of truth, as science becomes a ...
Dax Ovid, Zeus Leonardo
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Epilepsy‐Associated Variants of a Single SCN1A Codon Exhibit Divergent Functional Properties
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Pathogenic variants in SCN1A, which encodes the voltage‐gated sodium channel NaV1.1, are associated with multiple epilepsy syndromes exhibiting a range of clinical severity. SCN1A variants are reported in different syndromes, including Dravet syndrome, which is associated with loss‐of‐function, whereas neonatal/infantile‐onset ...
Lanie N. Liebovitz +3 more
wiley +1 more source
Histopathological Evidence of Neurodegenerative Pathology in Epilepsy: A Systematic Review
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Epilepsy affects > 50 million people worldwide and is associated with a disproportionate burden of cognitive impairment. Emerging evidence suggests that neurodegenerative proteinopathies, particularly hyperphosphorylated tau (p‐tau) and amyloid‐β (Aβ), may contribute to cognitive dysfunction in people with epilepsy (PWE), even in the absence ...
Syeda Amrah Hashmi +7 more
wiley +1 more source
Arthritis Care &Research, EarlyView.Objective We aimed to estimate the prevalence and cumulative incidence of hydroxychloroquine retinopathy (HCQ‐R) and its risk factors among patients receiving long‐term HCQ with rheumatic diseases through a systematic review and meta‐analysis of observational studies that used spectral‐domain optical coherence tomography (SD‐OCT) for screening ...
Narsis Daftarian +4 more
wiley +1 more source
Frontiers in Psychology, 2021 The lexical system of Hong Kong Cantonese has been heavily shaped by the local trilingual environment. The development of cultural- and language-specific norms for Hong Kong Cantonese is fundamental for understanding how the speaker population organize ...
Bing Li +7 more
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Ocular and Systemic Findings in COL2A1 and COL11A1 Stickler Syndrome
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Stickler syndrome is most commonly caused by variants in COL2A1 and COL11A1 genes. The purpose of this study was to describe genetic variants and phenotypes in COL2A1 and COL11A1 Stickler syndrome. We performed a retrospective genotype–phenotype evaluation of COL2A1 and COL11A1 Stickler syndrome subjects. Thirty‐two subjects with COL2A1 and 13
Aileen G. MacLachlan +5 more
wiley +1 more source