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| pubmed-article:20697050 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:20697050 | pubmed:dateCreated | 2010-8-10 | lld:pubmed |
| pubmed-article:20697050 | pubmed:abstractText | To report the clinical, genetic, neuroimaging, and neuropathologic studies of patients with the hereditary cerebral hemorrhage with amyloidosis linked to the APP E693K mutation. | lld:pubmed |
| pubmed-article:20697050 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:20697050 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20697050 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:20697050 | pubmed:issn | 1538-3687 | lld:pubmed |
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| pubmed-article:20697050 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20697050 | pubmed:volume | 67 | lld:pubmed |
| pubmed-article:20697050 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20697050 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20697050 | pubmed:pagination | 987-95 | lld:pubmed |
| pubmed-article:20697050 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:20697050 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:20697050 | pubmed:articleTitle | Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP. | lld:pubmed |
| pubmed-article:20697050 | pubmed:affiliation | Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11-20133, Milan, Italy. | lld:pubmed |
| pubmed-article:20697050 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20697050 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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