| pubmed-article:15547923 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15547923 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
| pubmed-article:15547923 | lifeskim:mentions | umls-concept:C0012634 | lld:lifeskim |
| pubmed-article:15547923 | lifeskim:mentions | umls-concept:C0019618 | lld:lifeskim |
| pubmed-article:15547923 | lifeskim:mentions | umls-concept:C0522498 | lld:lifeskim |
| pubmed-article:15547923 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:15547923 | pubmed:dateCreated | 2005-7-19 | lld:pubmed |
| pubmed-article:15547923 | pubmed:abstractText | Histiocytic disorders are currently identified by their component cells. The non-Langerhans Cell Histiocytoses (non-LCH) are a group of disorders defined by the accumulation of histiocytes that do not meet the phenotypic criteria for the diagnosis of Langerhans cells (LCs). The non-LCH consist of a long list of diverse disorders which have been difficult to categorize. A conceptual way to think of these disorders that make them less confusing and easier to remember is proposed based on immunophenotyping and clinical presentation. | lld:pubmed |
| pubmed-article:15547923 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15547923 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15547923 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15547923 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15547923 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:15547923 | pubmed:issn | 1545-5009 | lld:pubmed |
| pubmed-article:15547923 | pubmed:author | pubmed-author:JaffeRonaldR | lld:pubmed |
| pubmed-article:15547923 | pubmed:author | pubmed-author:WeitzmanSheil... | lld:pubmed |
| pubmed-article:15547923 | pubmed:copyrightInfo | (c) 2005 Wiley-Liss, Inc. | lld:pubmed |
| pubmed-article:15547923 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15547923 | pubmed:volume | 45 | lld:pubmed |
| pubmed-article:15547923 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15547923 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15547923 | pubmed:pagination | 256-64 | lld:pubmed |
| pubmed-article:15547923 | pubmed:dateRevised | 2009-1-12 | lld:pubmed |
| pubmed-article:15547923 | pubmed:meshHeading | pubmed-meshheading:15547923... | lld:pubmed |
| pubmed-article:15547923 | pubmed:meshHeading | pubmed-meshheading:15547923... | lld:pubmed |
| pubmed-article:15547923 | pubmed:meshHeading | pubmed-meshheading:15547923... | lld:pubmed |
| pubmed-article:15547923 | pubmed:meshHeading | pubmed-meshheading:15547923... | lld:pubmed |
| pubmed-article:15547923 | pubmed:meshHeading | pubmed-meshheading:15547923... | lld:pubmed |
| pubmed-article:15547923 | pubmed:meshHeading | pubmed-meshheading:15547923... | lld:pubmed |
| pubmed-article:15547923 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:15547923 | pubmed:articleTitle | Uncommon histiocytic disorders: the non-Langerhans cell histiocytoses. | lld:pubmed |
| pubmed-article:15547923 | pubmed:affiliation | Department of Pediatrics, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada. sheila.weitzman@sickkids.ca | lld:pubmed |
| pubmed-article:15547923 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15547923 | pubmed:publicationType | Review | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15547923 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15547923 | lld:pubmed |
