pubmed-article:18985676 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18985676 | lifeskim:mentions | umls-concept:C1261473 | lld:lifeskim |
pubmed-article:18985676 | lifeskim:mentions | umls-concept:C2699414 | lld:lifeskim |
pubmed-article:18985676 | lifeskim:mentions | umls-concept:C1516477 | lld:lifeskim |
pubmed-article:18985676 | lifeskim:mentions | umls-concept:C0684224 | lld:lifeskim |
pubmed-article:18985676 | lifeskim:mentions | umls-concept:C0220611 | lld:lifeskim |
pubmed-article:18985676 | lifeskim:mentions | umls-concept:C0002793 | lld:lifeskim |
pubmed-article:18985676 | lifeskim:mentions | umls-concept:C0033105 | lld:lifeskim |
pubmed-article:18985676 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
pubmed-article:18985676 | pubmed:issue | 11 | lld:pubmed |
pubmed-article:18985676 | pubmed:dateCreated | 2008-12-1 | lld:pubmed |
pubmed-article:18985676 | pubmed:abstractText | Anapalsia is rare in childhood rhabdomyosarcoma and has not been included in the International Classification of Rhabdomyosarcoma (ICR). A recent review of cases from the Soft Tissue Sarcoma Committee of the Children's Oncology Group (COG) suggests that anaplasia might be more common than previously reported and may impact clinical outcome. | lld:pubmed |
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pubmed-article:18985676 | pubmed:language | eng | lld:pubmed |
pubmed-article:18985676 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18985676 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:18985676 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18985676 | pubmed:month | Dec | lld:pubmed |
pubmed-article:18985676 | pubmed:issn | 0008-543X | lld:pubmed |
pubmed-article:18985676 | pubmed:author | pubmed-author:LynchJamesJ | lld:pubmed |
pubmed-article:18985676 | pubmed:author | pubmed-author:MeyerWilliamW | lld:pubmed |
pubmed-article:18985676 | pubmed:author | pubmed-author:TeotLisaL | lld:pubmed |
pubmed-article:18985676 | pubmed:author | pubmed-author:BridgeJuliaJ | lld:pubmed |
pubmed-article:18985676 | pubmed:author | pubmed-author:ParhamDavidD | lld:pubmed |
pubmed-article:18985676 | pubmed:author | pubmed-author:PappoAlbertoA | lld:pubmed |
pubmed-article:18985676 | pubmed:author | pubmed-author:QualmanStephe... | lld:pubmed |
pubmed-article:18985676 | pubmed:copyrightInfo | (c) 2008 American Cancer Society | lld:pubmed |
pubmed-article:18985676 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18985676 | pubmed:day | 1 | lld:pubmed |
pubmed-article:18985676 | pubmed:volume | 113 | lld:pubmed |
pubmed-article:18985676 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18985676 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18985676 | pubmed:pagination | 3242-7 | lld:pubmed |
pubmed-article:18985676 | pubmed:dateRevised | 2011-9-26 | lld:pubmed |
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pubmed-article:18985676 | pubmed:meshHeading | pubmed-meshheading:18985676... | lld:pubmed |
pubmed-article:18985676 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18985676 | pubmed:articleTitle | Prevalence and clinical impact of anaplasia in childhood rhabdomyosarcoma : a report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group. | lld:pubmed |
pubmed-article:18985676 | pubmed:affiliation | Center for Childhood Cancer, Columbus, Ohio, USA. | lld:pubmed |
pubmed-article:18985676 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18985676 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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