| pubmed-article:10225357 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10225357 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:10225357 | lifeskim:mentions | umls-concept:C1556085 | lld:lifeskim |
| pubmed-article:10225357 | lifeskim:mentions | umls-concept:C0013421 | lld:lifeskim |
| pubmed-article:10225357 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:10225357 | lifeskim:mentions | umls-concept:C1851945 | lld:lifeskim |
| pubmed-article:10225357 | lifeskim:mentions | umls-concept:C1853719 | lld:lifeskim |
| pubmed-article:10225357 | lifeskim:mentions | umls-concept:C1540039 | lld:lifeskim |
| pubmed-article:10225357 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:10225357 | pubmed:dateCreated | 1999-9-8 | lld:pubmed |
| pubmed-article:10225357 | pubmed:abstractText | Primary dystonia is a clinically and genetically heterogeneous movement disorder characterized by sustained involuntary muscle contractions causing repetitive movements and/or abnormal postures. Recently, the gene locus (DYT1) and mutation responsible for a substantial number of cases suffering from early-onset primary dystonia was described. Here we report 2 German families and 1 sporadic patient with early-onset dystonia due to the DYT1 mutation in order to illustrate the variability of clinical manifestation within this molecularly defined entity. We demonstrate that writer's cramp or focal cervical dystonia is a clinical presentation of DYT1 as well as generalized dystonia. | lld:pubmed |
| pubmed-article:10225357 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10225357 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10225357 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:10225357 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10225357 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10225357 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10225357 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10225357 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:10225357 | pubmed:issn | 0001-6314 | lld:pubmed |
| pubmed-article:10225357 | pubmed:author | pubmed-author:SchwendemannG... | lld:pubmed |
| pubmed-article:10225357 | pubmed:author | pubmed-author:EbkeMM | lld:pubmed |
| pubmed-article:10225357 | pubmed:author | pubmed-author:BeneckeRR | lld:pubmed |
| pubmed-article:10225357 | pubmed:author | pubmed-author:KesslerK RKR | lld:pubmed |
| pubmed-article:10225357 | pubmed:author | pubmed-author:FerbertAA | lld:pubmed |
| pubmed-article:10225357 | pubmed:author | pubmed-author:AuburgerGG | lld:pubmed |
| pubmed-article:10225357 | pubmed:author | pubmed-author:ErbguthFF | lld:pubmed |
| pubmed-article:10225357 | pubmed:author | pubmed-author:LeubeBB | lld:pubmed |
| pubmed-article:10225357 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10225357 | pubmed:volume | 99 | lld:pubmed |
| pubmed-article:10225357 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10225357 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10225357 | pubmed:pagination | 248-51 | lld:pubmed |
| pubmed-article:10225357 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:meshHeading | pubmed-meshheading:10225357... | lld:pubmed |
| pubmed-article:10225357 | pubmed:year | 1999 | lld:pubmed |
| pubmed-article:10225357 | pubmed:articleTitle | Phenotypic variability of the DYT1 mutation in German dystonia patients. | lld:pubmed |
| pubmed-article:10225357 | pubmed:affiliation | Dept of Neurology, Heinrich-Heine-University, Düsseldorf, Germany. | lld:pubmed |
| pubmed-article:10225357 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10225357 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:10225357 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:10225357 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:10225357 | lld:pubmed |
