| pubmed-article:15754282 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15754282 | lifeskim:mentions | umls-concept:C0012634 | lld:lifeskim |
| pubmed-article:15754282 | lifeskim:mentions | umls-concept:C0155765 | lld:lifeskim |
| pubmed-article:15754282 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:15754282 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
| pubmed-article:15754282 | lifeskim:mentions | umls-concept:C0056207 | lld:lifeskim |
| pubmed-article:15754282 | lifeskim:mentions | umls-concept:C1826260 | lld:lifeskim |
| pubmed-article:15754282 | lifeskim:mentions | umls-concept:C0004083 | lld:lifeskim |
| pubmed-article:15754282 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:15754282 | pubmed:dateCreated | 2005-3-8 | lld:pubmed |
| pubmed-article:15754282 | pubmed:abstractText | cblC disease is a cause of hemolytic uremic syndrome (HUS), which has been primarily described in neonates and infants with severe renal and neurological lesions. | lld:pubmed |
| pubmed-article:15754282 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:15754282 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:15754282 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15754282 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:15754282 | pubmed:issn | 1523-6838 | lld:pubmed |
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| pubmed-article:15754282 | pubmed:author | pubmed-author:FavierRémiR | lld:pubmed |
| pubmed-article:15754282 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:15754282 | pubmed:volume | 45 | lld:pubmed |
| pubmed-article:15754282 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15754282 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15754282 | pubmed:pagination | 588-95 | lld:pubmed |
| pubmed-article:15754282 | pubmed:dateRevised | 2005-11-17 | lld:pubmed |
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| pubmed-article:15754282 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:15754282 | pubmed:articleTitle | Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation. | lld:pubmed |
| pubmed-article:15754282 | pubmed:affiliation | Department of Pediatric Nephrology, Hôpital Armand-Trousseau, Paris, France. | lld:pubmed |
| pubmed-article:15754282 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15754282 | pubmed:publicationType | Case Reports | lld:pubmed |
| entrez-gene:3075 | entrezgene:pubmed | pubmed-article:15754282 | lld:entrezgene |
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| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15754282 | lld:pubmed |
