Multi-Analytical and Non-Invasive Approach for Characterising Blackened Areas of Originally Blue Paints. [PDF]
Labate M+5 more
europepmc +1 more source
Studying attention to IPCC climate change maps with mobile eye-tracking. [PDF]
Gulhan D, Bahrami B, Deroy O.
europepmc +1 more source
Novel Phenotypes and Deep Intronic Variant Expand TH‐Associated Dopa‐Responsive Dystonia Spectrum
ABSTRACT Approximately 20% of dopa‐responsive dystonia (DRD) cases remain genetically unresolved. Using whole‐genome sequencing, we identified two TH variants in a young DRD patient, including a novel deep intronic variant. Minigene assays confirmed that this variant causes aberrant splicing.
Xiaosheng Zheng+6 more
wiley +1 more source
The effect of social factors on eye movements made when judging the aesthetic merit of figurative paintings. [PDF]
Trawiński T+3 more
europepmc +1 more source
ABSTRACT Objective Certain frontotemporal lobar degeneration subtypes, including TDP‐A and B, can either occur sporadically or in association with specific genetic mutations. It is uncertain whether syndromic or imaging features previously associated with these patient groups are subtype or genotype specific.
Sean Coulborn+17 more
wiley +1 more source
A Study on Pigment Composition of Buddhist Cave Paintings Based on Hyperspectral Technology. [PDF]
Shi X, Lin X, Lei Y, Wu J, Lv X, Zhou Y.
europepmc +1 more source
FGF14 GAA Intronic Expansion in Unsolved Adult‐Onset Ataxia in the Care4Rare Canada Consortium
ABSTRACT Background and Objectives Spinocerebellar ataxias (SCA) represent a clinically and genetically heterogeneous group of progressive neurodegenerative diseases with prominent cerebellar atrophy. Recently, a novel pathogenic repeat expansion in intron 1 of FGF14 was identified, causing adult‐onset SCA (SCA27B). We aimed to determine the proportion
Alexanne Cuillerier+20 more
wiley +1 more source
Age-adapted painting descriptions change the viewing behavior of young visitors to the Rijksmuseum. [PDF]
Walker F+9 more
europepmc +1 more source
Early Language Impairment as an Integral Part of the Cognitive Phenotype in Huntington's Disease
ABSTRACT Objective Huntington's disease (HD) speech/language disorders have typically been attributed to motor and executive impairment due to striatal dysfunction. In‐depth study of linguistic skills and the role of extrastriatal structures in HD is scarce.
Arnau Puig‐Davi+13 more
wiley +1 more source
Reply to the letter: What can paintings teach us? [PDF]
Di Cosimo S+7 more
europepmc +1 more source