| pubmed-article:9489526 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9489526 | lifeskim:mentions | umls-concept:C1457887 | lld:lifeskim |
| pubmed-article:9489526 | lifeskim:mentions | umls-concept:C0020179 | lld:lifeskim |
| pubmed-article:9489526 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:9489526 | lifeskim:mentions | umls-concept:C1392786 | lld:lifeskim |
| pubmed-article:9489526 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
| pubmed-article:9489526 | lifeskim:mentions | umls-concept:C1742737 | lld:lifeskim |
| pubmed-article:9489526 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:9489526 | pubmed:dateCreated | 1998-3-24 | lld:pubmed |
| pubmed-article:9489526 | pubmed:abstractText | Huntington's disease is a neurodegenerative disorder due to an excessive number of CAG repeats in the IT15 gene on chromosome 4. The first symptoms are typically choreic movements or psychiatric disorders, whereas global cognitive decline generally becomes obvious later. This study was aimed at detecting early subtle cognitive deficits in asymptomatic gene carriers. | lld:pubmed |
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| pubmed-article:9489526 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9489526 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9489526 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:9489526 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9489526 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:9489526 | pubmed:issn | 0022-3050 | lld:pubmed |
| pubmed-article:9489526 | pubmed:author | pubmed-author:AgidYY | lld:pubmed |
| pubmed-article:9489526 | pubmed:author | pubmed-author:PillonBB | lld:pubmed |
| pubmed-article:9489526 | pubmed:author | pubmed-author:FeingoldJJ | lld:pubmed |
| pubmed-article:9489526 | pubmed:author | pubmed-author:DeweerBB | lld:pubmed |
| pubmed-article:9489526 | pubmed:author | pubmed-author:DuboisBB | lld:pubmed |
| pubmed-article:9489526 | pubmed:author | pubmed-author:DürrAA | lld:pubmed |
| pubmed-article:9489526 | pubmed:author | pubmed-author:BriceAA | lld:pubmed |
| pubmed-article:9489526 | pubmed:author | pubmed-author:DohmCC | lld:pubmed |
| pubmed-article:9489526 | pubmed:author | pubmed-author:Hahn-BarmaVV | lld:pubmed |
| pubmed-article:9489526 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9489526 | pubmed:volume | 64 | lld:pubmed |
| pubmed-article:9489526 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9489526 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9489526 | pubmed:pagination | 172-7 | lld:pubmed |
| pubmed-article:9489526 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:9489526 | pubmed:meshHeading | pubmed-meshheading:9489526-... | lld:pubmed |
| pubmed-article:9489526 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9489526 | pubmed:articleTitle | Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriers. | lld:pubmed |
| pubmed-article:9489526 | pubmed:affiliation | Fédération de Neurologie and INSERM U.289, Hôpital de la Salpêtrière, Paris, France. | lld:pubmed |
| pubmed-article:9489526 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9489526 | pubmed:publicationType | Clinical Trial | lld:pubmed |
| pubmed-article:9489526 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:9489526 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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