| pubmed-article:15335440 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15335440 | lifeskim:mentions | umls-concept:C0017382 | lld:lifeskim |
| pubmed-article:15335440 | lifeskim:mentions | umls-concept:C0017398 | lld:lifeskim |
| pubmed-article:15335440 | lifeskim:mentions | umls-concept:C0338451 | lld:lifeskim |
| pubmed-article:15335440 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:15335440 | pubmed:dateCreated | 2004-8-31 | lld:pubmed |
| pubmed-article:15335440 | pubmed:abstractText | Frontotemporal dementia (FTD) is a neurodegenerative disease with early symptoms of personality change and/or language disorder. Approximately 40% of individuals with FTD have a family history of dementia; however, in our experience, less than 10% have clear autosomal dominant inheritance. Mutations in the microtubule-associated protein tau (MAPT) gene have been reported in up to 50% of hereditary cases, but are unusual except in families with more than 3 individuals with FTD. The genetics of FTD is complicated by clinical heterogeneity, variable expression, phenocopies, misdiagnoses, and lost family histories. The objective of this paper is to enable physicians to recognize hereditary patterns and genetic concerns of FTD families and to understand genetic counseling strategies. | lld:pubmed |
| pubmed-article:15335440 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15335440 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15335440 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15335440 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15335440 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15335440 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15335440 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15335440 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15335440 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15335440 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15335440 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15335440 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:15335440 | pubmed:issn | 1074-7931 | lld:pubmed |
| pubmed-article:15335440 | pubmed:author | pubmed-author:MillerBruce... | lld:pubmed |
| pubmed-article:15335440 | pubmed:author | pubmed-author:GrossmanMurra... | lld:pubmed |
| pubmed-article:15335440 | pubmed:author | pubmed-author:FarmerJennife... | lld:pubmed |
| pubmed-article:15335440 | pubmed:author | pubmed-author:GoldmanJill... | lld:pubmed |
| pubmed-article:15335440 | pubmed:author | pubmed-author:WilhelmsenKir... | lld:pubmed |
| pubmed-article:15335440 | pubmed:author | pubmed-author:Van... | lld:pubmed |
| pubmed-article:15335440 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15335440 | pubmed:volume | 10 | lld:pubmed |
| pubmed-article:15335440 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15335440 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15335440 | pubmed:pagination | 227-34 | lld:pubmed |
| pubmed-article:15335440 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
| pubmed-article:15335440 | pubmed:meshHeading | pubmed-meshheading:15335440... | lld:pubmed |
| pubmed-article:15335440 | pubmed:meshHeading | pubmed-meshheading:15335440... | lld:pubmed |
| pubmed-article:15335440 | pubmed:meshHeading | pubmed-meshheading:15335440... | lld:pubmed |
| pubmed-article:15335440 | pubmed:meshHeading | pubmed-meshheading:15335440... | lld:pubmed |
| pubmed-article:15335440 | pubmed:meshHeading | pubmed-meshheading:15335440... | lld:pubmed |
| pubmed-article:15335440 | pubmed:meshHeading | pubmed-meshheading:15335440... | lld:pubmed |
| pubmed-article:15335440 | pubmed:meshHeading | pubmed-meshheading:15335440... | lld:pubmed |
| pubmed-article:15335440 | pubmed:meshHeading | pubmed-meshheading:15335440... | lld:pubmed |
| pubmed-article:15335440 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15335440 | pubmed:articleTitle | Frontotemporal dementia: genetics and genetic counseling dilemmas. | lld:pubmed |
| pubmed-article:15335440 | pubmed:affiliation | Memory and Aging Center, University of California, San Francisco, Department of Neurology, San Francisco, California 94143-1207, USA. jgoldman@memory.ucsf.edu | lld:pubmed |
| pubmed-article:15335440 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15335440 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:15335440 | pubmed:publicationType | Review | lld:pubmed |
| pubmed-article:15335440 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15335440 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15335440 | lld:pubmed |
