A common neurocognitive phenotype of Turner syndrome (TS) includes coincident deficits in math and visuospatial reasoning while overall IQ remains intact. However, research has highlighted disparities in the relationship between these properties in women with TS, suggesting that not all visuospatial domains are equally related to mathematics in this group. Here, we present findings from a longitudinal investigation of visuospatial processing and its relationship to math performance in adolescent girls with TS and age-matched healthy controls. Participants completed a standardized battery of math and visuospatial tests once a year for 4 years. Linear mixed effects modeling was used to examine the relationship between mathematics and each vis...
Turner syndrome is associated with spatial and numerical cognitive impairments. We hypothesized that...
Turner syndrome (TS) is a genetic disorder, affecting 1/2500 to 1/3000 live female births, induced b...
Children with one of two genetic disorders (chromosome 22q11.2 deletion syndrome and Turner syndrome...
Individuals with Mathematics Learning Disabilities have persistent mathematics underperformance but ...
<div><p>Most studies on magnitude representation have focused on the visual modality with no possibi...
Most studies on magnitude representation have focused on the visual modality with no possibility of ...
Individuals with Mathematics Learning Disabilities have persistent mathematics underperformance but ...
Turner syndrome (TS) is a neurogenetic disorder characterized by the absence of one X chromosome in ...
The association of spatial deficits and lower Performance IQ (PIQ) scores in Turner Syndrome Patient...
Most studies on early magnitude representation focused on the visual modality with no possibility to...
Cross-syndrome comparisons offer an important window onto understanding heterogeneity in mathematica...
Item does not contain fulltextWe reviewed the literature on Turner Syndrome (TS) from 1962 until Mar...
Turner syndrome is a genetic disorder that results from an abnormal or missing X chromosome in femal...
Item does not contain fulltextWe reviewed the literature on Turner Syndrome (TS) from 1962 until Mar...
Compared short-term verbal memory, sustained attention, and impulsivity in 13 children with Turner s...
Turner syndrome is associated with spatial and numerical cognitive impairments. We hypothesized that...
Turner syndrome (TS) is a genetic disorder, affecting 1/2500 to 1/3000 live female births, induced b...
Children with one of two genetic disorders (chromosome 22q11.2 deletion syndrome and Turner syndrome...
Individuals with Mathematics Learning Disabilities have persistent mathematics underperformance but ...
<div><p>Most studies on magnitude representation have focused on the visual modality with no possibi...
Most studies on magnitude representation have focused on the visual modality with no possibility of ...
Individuals with Mathematics Learning Disabilities have persistent mathematics underperformance but ...
Turner syndrome (TS) is a neurogenetic disorder characterized by the absence of one X chromosome in ...
The association of spatial deficits and lower Performance IQ (PIQ) scores in Turner Syndrome Patient...
Most studies on early magnitude representation focused on the visual modality with no possibility to...
Cross-syndrome comparisons offer an important window onto understanding heterogeneity in mathematica...
Item does not contain fulltextWe reviewed the literature on Turner Syndrome (TS) from 1962 until Mar...
Turner syndrome is a genetic disorder that results from an abnormal or missing X chromosome in femal...
Item does not contain fulltextWe reviewed the literature on Turner Syndrome (TS) from 1962 until Mar...
Compared short-term verbal memory, sustained attention, and impulsivity in 13 children with Turner s...
Turner syndrome is associated with spatial and numerical cognitive impairments. We hypothesized that...
Turner syndrome (TS) is a genetic disorder, affecting 1/2500 to 1/3000 live female births, induced b...
Children with one of two genetic disorders (chromosome 22q11.2 deletion syndrome and Turner syndrome...