| pubmed-article:21480468 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21480468 | lifeskim:mentions | umls-concept:C0008059 | lld:lifeskim |
| pubmed-article:21480468 | lifeskim:mentions | umls-concept:C0037889 | lld:lifeskim |
| pubmed-article:21480468 | lifeskim:mentions | umls-concept:C0019029 | lld:lifeskim |
| pubmed-article:21480468 | lifeskim:mentions | umls-concept:C0312853 | lld:lifeskim |
| pubmed-article:21480468 | lifeskim:mentions | umls-concept:C0149783 | lld:lifeskim |
| pubmed-article:21480468 | lifeskim:mentions | umls-concept:C1704419 | lld:lifeskim |
| pubmed-article:21480468 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:21480468 | pubmed:dateCreated | 2011-6-14 | lld:pubmed |
| pubmed-article:21480468 | pubmed:abstractText | The course of hereditary spherocytosis (HS) may be subject to hemolytic episodes, sometimes requiring blood transfusion. The aim of this study was to evaluate the efficacy of a short course of steroid therapy in elevating hemoglobin levels during hemolytic crisis. | lld:pubmed |
| pubmed-article:21480468 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21480468 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21480468 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21480468 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21480468 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21480468 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21480468 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21480468 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21480468 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:21480468 | pubmed:issn | 1545-5017 | lld:pubmed |
| pubmed-article:21480468 | pubmed:author | pubmed-author:YanivIsaacI | lld:pubmed |
| pubmed-article:21480468 | pubmed:author | pubmed-author:BallinAmiA | lld:pubmed |
| pubmed-article:21480468 | pubmed:author | pubmed-author:TamaryHannahH | lld:pubmed |
| pubmed-article:21480468 | pubmed:author | pubmed-author:YacobovichJoa... | lld:pubmed |
| pubmed-article:21480468 | pubmed:author | pubmed-author:Barzilai-Bire... | lld:pubmed |
| pubmed-article:21480468 | pubmed:author | pubmed-author:Waisbourd-Zin... | lld:pubmed |
| pubmed-article:21480468 | pubmed:author | pubmed-author:SaabHitamH | lld:pubmed |
| pubmed-article:21480468 | pubmed:author | pubmed-author:ZoldanMeirahM | lld:pubmed |
| pubmed-article:21480468 | pubmed:copyrightInfo | Copyright © 2011 Wiley-Liss, Inc. | lld:pubmed |
| pubmed-article:21480468 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21480468 | pubmed:volume | 57 | lld:pubmed |
| pubmed-article:21480468 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21480468 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21480468 | pubmed:pagination | 303-5 | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:meshHeading | pubmed-meshheading:21480468... | lld:pubmed |
| pubmed-article:21480468 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21480468 | pubmed:articleTitle | Steroid therapy may be effective in augmenting hemoglobin levels during hemolytic crises in children with hereditary spherocytosis. | lld:pubmed |
| pubmed-article:21480468 | pubmed:affiliation | Department of Pediatrics, Edith Wolfson Medical Center, Holon, Israel. ballin@wolfson.health.gov.il | lld:pubmed |
| pubmed-article:21480468 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21480468 | pubmed:publicationType | Comparative Study | lld:pubmed |
