The primary cognitive deficit among males with fragile X-associated tremor/ataxia syndrome (FXTAS) is a dysexecutive syndrome. - Test2 - elhamkhani - TriplyDB

The primary cognitive deficit among males with fragile X-associated tremor/ataxia syndrome (FXTAS) is a dysexecutive syndrome.

The primary cognitive deficit among males with fragile X-associated tremor/ataxia syndrome (FXTAS) is a dysexecutive syndrome.

http://www.wikidata.org/entity/Q33901895

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The fragile X mental retardation 1 gene (FMR1): historical perspective, phenotypes, mechanism, pathology, and epidemiology Fragile X tremor ataxia syndrome and white matter dementia.Neural substrates of executive dysfunction in fragile X-associated tremor/ataxia syndrome (FXTAS): a brain potential study.Memantine effects on verbal memory in fragile X-associated tremor/ataxia syndrome (FXTAS): a double-blind brain potential study.Fibroblast phenotype in male carriers of FMR1 premutation alleles Executive function (capacity for behavioral self-regulation) and decline predicted mortality in a longitudinal study in Southern Colorado Broad clinical involvement in a family affected by the fragile X premutation.Age-dependent cognitive impairment in a Drosophila fragile X model and its pharmacological rescue Associated features in females with an FMR1 premutation The cognitive neuropsychological phenotype of carriers of the FMR1 premutation.Lifespan changes in working memory in fragile X premutation males.Eye movements reveal impaired inhibitory control in adult male fragile X premutation carriers asymptomatic for FXTAS.Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome.COGNITIVE DYSFUNCTION IN FMR1 PREMUTATION CARRIERS.PSYCHIATRIC DISORDERS ASSOCIATED WITH FXTAS.Mouse models of the fragile x premutation and the fragile X associated tremor/ataxia syndrome.Temporal dynamics of attentional selection in adult male carriers of the fragile X premutation allele and adult controls.Selective executive markers of at-risk profiles associated with the fragile X premutation.Ages of Onset of Mood and Anxiety Disorders in Fragile X Premutation Carriers Assessment of patient and caregiver needs in fragile X-associated tremor/ataxia syndrome by utilizing Q-sort methodology.Functional status of men with the fragile X premutation, with and without the tremor/ataxia syndrome (FXTAS).A cross-sectional analysis of orienting of visuospatial attention in child and adult carriers of the fragile X premutation.White matter disease and cognitive impairment in FMR1 premutation carriers.FMR1 premutation and full mutation molecular mechanisms related to autism.Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts.Young adult male carriers of the fragile X premutation exhibit genetically modulated impairments in visuospatial tasks controlled for psychomotor speed.Memantine Improves Attentional Processes in Fragile X-Associated Tremor/Ataxia Syndrome: Electrophysiological Evidence from a Randomized Controlled Trial.Language dysfluencies in females with the FMR1 premutation.Fragile X syndrome: an aging perspective.New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS)Plasma Biomarkers for Monitoring Brain Pathophysiology in FMR1 Premutation Carriers.A multimodal imaging analysis of subcortical gray matter in fragile X premutation carriers.Caregiver Burden in Fragile X Families.Abnormal semantic processing in females with fragile X-associated tremor/ataxia syndrome.Phenotypes of hypofrontality in older female fragile X premutation carriers Neuropathological, clinical and molecular pathology in female fragile X premutation carriers with and without FXTAS.Understanding the neuropsychiatric phenotype of fragile X-associated tremor ataxia syndrome: a systematic review.Prevalence and predictors of subjective memory complaints in adult male carriers of the FMR1 premutation.Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders.Executive Dysfunction in Female FMR1 Premutation Carriers.

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The primary cognitive deficit among males with fragile X-associated tremor/ataxia syndrome (FXTAS) is a dysexecutive syndrome.

http://www.wikidata.org/entity/Q33901895

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2008 nî lūn-bûn

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2008 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2008 թվականի փետրվարին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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The primary cognitive deficit ...... S) is a dysexecutive syndrome.

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The primary cognitive deficit ...... S) is a dysexecutive syndrome.

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The primary cognitive deficit ...... S) is a dysexecutive syndrome.

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The primary cognitive deficit ...... S) is a dysexecutive syndrome.

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The primary cognitive deficit ...... S) is a dysexecutive syndrome.

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The primary cognitive deficit ...... S) is a dysexecutive syndrome.

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Neuropsychology, Development and Cognition. Section A: Journal of Clinical and Experimental Neuropsychology

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The primary cognitive deficit ...... S) is a dysexecutive syndrome.

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Angela G Brega

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Ann Reynolds

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David Hessl

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Flora Tassone

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Glenn Goodrich

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Jennifer B Cogswell

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Jim Grigsby

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Karen Engle

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Lanee S Bounds

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Marsha J Paulich

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P2860

Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation

The fragile-X premutation: a maturing perspective.

“Mini-mental state”

The moderator–mediator variable distinction in social psychological research: Conceptual, strategic, and statistical considerations

Fluid intelligence after frontal lobe lesions

Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population

The evolution and pathology of frontotemporal dementia

SPSS and SAS procedures for estimating indirect effects in simple mediation models

Functional architecture of basal ganglia circuits: neural substrates of parallel processing

Reduced recruitment of motor association areas during bimanual coordination in concert pianists.

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10.1080/13803390701819044

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8

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30

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fragile X-associated tremor/ataxia syndrome

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4098148

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