| pubmed-article:9602208 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9602208 | lifeskim:mentions | umls-concept:C0037047 | lld:lifeskim |
| pubmed-article:9602208 | lifeskim:mentions | umls-concept:C0019425 | lld:lifeskim |
| pubmed-article:9602208 | lifeskim:mentions | umls-concept:C0019904 | lld:lifeskim |
| pubmed-article:9602208 | lifeskim:mentions | umls-concept:C0023234 | lld:lifeskim |
| pubmed-article:9602208 | lifeskim:mentions | umls-concept:C0584960 | lld:lifeskim |
| pubmed-article:9602208 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:9602208 | pubmed:dateCreated | 1998-6-18 | lld:pubmed |
| pubmed-article:9602208 | pubmed:abstractText | A family is described with three-generation transmission of factor V Leiden (a thrombophilic mutation that causes resistance to activated protein C). Legg-Perthes disease developed in three siblings in this family. The male proband and his sister were heterozygous for the mutation and had unilateral hip disease at age 2 years. The brother, who had bilateral hip disease, was homozygous. This novel family provides compelling evidence for the pathoetiologic role of familial thrombophilia in Legg-Perthes disease. | lld:pubmed |
| pubmed-article:9602208 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9602208 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9602208 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:9602208 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9602208 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9602208 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9602208 | pubmed:month | May | lld:pubmed |
| pubmed-article:9602208 | pubmed:issn | 0022-3476 | lld:pubmed |
| pubmed-article:9602208 | pubmed:author | pubmed-author:WandSS | lld:pubmed |
| pubmed-article:9602208 | pubmed:author | pubmed-author:RoyDD | lld:pubmed |
| pubmed-article:9602208 | pubmed:author | pubmed-author:WalzWW | lld:pubmed |
| pubmed-article:9602208 | pubmed:author | pubmed-author:GruppoRR | lld:pubmed |
| pubmed-article:9602208 | pubmed:author | pubmed-author:GlueckC JCJ | lld:pubmed |
| pubmed-article:9602208 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9602208 | pubmed:volume | 132 | lld:pubmed |
| pubmed-article:9602208 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9602208 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9602208 | pubmed:pagination | 885-8 | lld:pubmed |
| pubmed-article:9602208 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:meshHeading | pubmed-meshheading:9602208-... | lld:pubmed |
| pubmed-article:9602208 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9602208 | pubmed:articleTitle | Legg-Perthes disease in three siblings, two heterozygous and one homozygous for the factor V Leiden mutation. | lld:pubmed |
| pubmed-article:9602208 | pubmed:affiliation | Division of Hematology/Oncology, Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA. | lld:pubmed |
| pubmed-article:9602208 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9602208 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:9602208 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:9602208 | lld:pubmed |
