scholarly article | Q13442814 |
P356 | DOI | 10.1136/JMG.32.5.358 |
P8608 | Fatcat ID | release_a62hguitezdtlepe2jhg5ndoku |
P932 | PMC publication ID | 1050430 |
P698 | PubMed publication ID | 7616542 |
P5875 | ResearchGate publication ID | 15581688 |
P2093 | author name string | S A Simpson | |
J R Crawford | |||
L Blackmore | |||
P2860 | cites work | A polymorphic DNA marker genetically linked to Huntington's disease | Q34255139 |
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The Bender Gestalt: Use of clinical judgment versus recall scores in prediction of Huntington's disease | Q39762933 | ||
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Comparison of the Neuropsychological Deficits Associated With Early and Advanced Huntington's Disease | Q39859862 | ||
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Are there neuropsychologic manifestations of the gene for Huntington's disease in asymptomatic, at-risk individuals? | Q45293907 | ||
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Development of Neuropsychological Deficits in Huntington's Disease | Q45304965 | ||
The involvement of the frontal lobes in cognitive estimation | Q48184590 | ||
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A multiple choice type of the visual retention test | Q75449904 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Huntington's disease | Q190564 |
P304 | page(s) | 358-362 | |
P577 | publication date | 1995-05-01 | |
P1433 | published in | Journal of Medical Genetics | Q14640281 |
P1476 | title | Cognitive performance in UK sample of presymptomatic people carrying the gene for Huntington's disease | |
P478 | volume | 32 |
Q45295884 | A double blind evaluation of cognitive decline in a Norwegian cohort of asymptomatic carriers of Huntington's disease |
Q36317837 | Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriers |
Q45294018 | Benton Judgment of Line Orientation (JoLO) Test: A Brief and Useful Measure for Assessing Visuospatial Abilities in Manifest, but not Premanifest, Huntington's Disease |
Q45294446 | Cognitive changes in patients with Huntington's disease (HD) and asymptomatic carriers of the HD mutation--a longitudinal follow-up study |
Q45296651 | Cognitive dysfunction precedes neuropathology and motor abnormalities in the YAC128 mouse model of Huntington's disease. |
Q41990962 | Comparison of cognitive and UHDRS measures in monitoring disease progression in Huntington's disease: a 12-month longitudinal study |
Q35036671 | Future directions in research with presymptomatic individuals carrying the gene for Huntington's disease |
Q36924337 | Implicit and explicit aspects of sequence learning in pre-symptomatic Huntington's disease. |
Q33679114 | Intelligence indices in people with a high/low risk for developing Huntington's disease |
Q45306639 | Longitudinal study evaluating neuropsychological changes in so-called asymptomatic carriers of the Huntington's disease mutation after 1 year |
Q36914999 | Motor disorder in Huntington's disease begins as a dysfunction in error feedback control. |
Q33743709 | Motor-Language Coupling in Huntington's Disease Families |
Q36900144 | Neuropsychological stability over two years in asymptomatic carriers of the Huntington's disease mutation |
Q45293357 | Processing of "scripts" and frontal lobe function in Huntington's disease |
Q33861265 | Progression in prediagnostic Huntington disease |
Q30439699 | Risk-taking and pathological gambling behavior in Huntington's disease |
Q35460244 | Subtle changes among presymptomatic carriers of the Huntington's disease gene |
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