| pubmed-article:16116133 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16116133 | lifeskim:mentions | umls-concept:C0015576 | lld:lifeskim |
| pubmed-article:16116133 | lifeskim:mentions | umls-concept:C0332307 | lld:lifeskim |
| pubmed-article:16116133 | lifeskim:mentions | umls-concept:C1425979 | lld:lifeskim |
| pubmed-article:16116133 | lifeskim:mentions | umls-concept:C0314603 | lld:lifeskim |
| pubmed-article:16116133 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
| pubmed-article:16116133 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
| pubmed-article:16116133 | lifeskim:mentions | umls-concept:C0053776 | lld:lifeskim |
| pubmed-article:16116133 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:16116133 | pubmed:dateCreated | 2005-8-23 | lld:pubmed |
| pubmed-article:16116133 | pubmed:abstractText | Presented is the new kindred with autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 (16q-ADCA type III) associated with progressive hearing loss. By haplotype analysis, the critical interval was slightly narrowed to three megabase regions between GATA01 and D16S3095. Neuropathologic study of 16q-ADCA type III demonstrated characteristic shrinkage of Purkinje cell bodies surrounded by synaptophysin-immunoreactive amorphous material containing calbindin- and ubiquitin-positive granules. | lld:pubmed |
| pubmed-article:16116133 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16116133 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16116133 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:16116133 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16116133 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16116133 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:16116133 | pubmed:issn | 1526-632X | lld:pubmed |
| pubmed-article:16116133 | pubmed:author | pubmed-author:IshikawaKK | lld:pubmed |
| pubmed-article:16116133 | pubmed:author | pubmed-author:NoguchiYY | lld:pubmed |
| pubmed-article:16116133 | pubmed:author | pubmed-author:TasKK | lld:pubmed |
| pubmed-article:16116133 | pubmed:author | pubmed-author:KitamuraKK | lld:pubmed |
| pubmed-article:16116133 | pubmed:author | pubmed-author:KondoII | lld:pubmed |
| pubmed-article:16116133 | pubmed:author | pubmed-author:OwadaKK | lld:pubmed |
| pubmed-article:16116133 | pubmed:author | pubmed-author:MizusawaHH | lld:pubmed |
| pubmed-article:16116133 | pubmed:author | pubmed-author:NoguchiEE | lld:pubmed |
| pubmed-article:16116133 | pubmed:author | pubmed-author:IshidoYY | lld:pubmed |
| pubmed-article:16116133 | pubmed:author | pubmed-author:GomyodaMM | lld:pubmed |
| pubmed-article:16116133 | pubmed:author | pubmed-author:ArinamiTT | lld:pubmed |
| pubmed-article:16116133 | pubmed:author | pubmed-author:TorpTT | lld:pubmed |
| pubmed-article:16116133 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:16116133 | pubmed:day | 23 | lld:pubmed |
| pubmed-article:16116133 | pubmed:volume | 65 | lld:pubmed |
| pubmed-article:16116133 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16116133 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16116133 | pubmed:pagination | 629-32 | lld:pubmed |
| pubmed-article:16116133 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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| pubmed-article:16116133 | pubmed:meshHeading | pubmed-meshheading:16116133... | lld:pubmed |
| pubmed-article:16116133 | pubmed:meshHeading | pubmed-meshheading:16116133... | lld:pubmed |
| pubmed-article:16116133 | pubmed:meshHeading | pubmed-meshheading:16116133... | lld:pubmed |
| pubmed-article:16116133 | pubmed:meshHeading | pubmed-meshheading:16116133... | lld:pubmed |
| pubmed-article:16116133 | pubmed:meshHeading | pubmed-meshheading:16116133... | lld:pubmed |
| pubmed-article:16116133 | pubmed:meshHeading | pubmed-meshheading:16116133... | lld:pubmed |
| pubmed-article:16116133 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:16116133 | pubmed:articleTitle | A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III. | lld:pubmed |
| pubmed-article:16116133 | pubmed:affiliation | Department of Neurology and Neurological Science, Graduate School, Tokyo Medical and Dental University, 1-5-45 Yushima, Tokyo, Japan. | lld:pubmed |
| pubmed-article:16116133 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16116133 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16116133 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16116133 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16116133 | lld:pubmed |
