| pubmed-article:12611061 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:12611061 | lifeskim:mentions | umls-concept:C0025517 | lld:lifeskim |
| pubmed-article:12611061 | lifeskim:mentions | umls-concept:C0206153 | lld:lifeskim |
| pubmed-article:12611061 | lifeskim:mentions | umls-concept:C2323499 | lld:lifeskim |
| pubmed-article:12611061 | lifeskim:mentions | umls-concept:C1515895 | lld:lifeskim |
| pubmed-article:12611061 | pubmed:dateCreated | 2003-3-3 | lld:pubmed |
| pubmed-article:12611061 | pubmed:abstractText | Clinical experience for more than two decades has shown that allogeneic HCT may benefit some but not all patients with inherited metabolic diseases. The HCT procedure is most effective in presymptomatic patients and those with indolent forms of storage diseases but is ineffective in those with overt neurological symptoms or aggressive neonatal or infantile forms. HCT alone does not correct skeletal dysplasia in MPSs and may not prevent development or progression of the peripheral neuropathy in sphingolipidoses and ALD. Decisions regarding HCT in patients with storage diseases should be made by investigators knowledgeable about these diseases, with judicious use of laboratory and clinical resources necessary to reach the best therapeutic decision for the individual patient. | lld:pubmed |
| pubmed-article:12611061 | pubmed:language | eng | lld:pubmed |
| pubmed-article:12611061 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12611061 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:12611061 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12611061 | pubmed:issn | 0939-5555 | lld:pubmed |
| pubmed-article:12611061 | pubmed:author | pubmed-author:YeagerA MAM | lld:pubmed |
| pubmed-article:12611061 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:12611061 | pubmed:volume | 81 Suppl 2 | lld:pubmed |
| pubmed-article:12611061 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12611061 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12611061 | pubmed:pagination | S16-9 | lld:pubmed |
| pubmed-article:12611061 | pubmed:dateRevised | 2005-11-16 | lld:pubmed |
| pubmed-article:12611061 | pubmed:meshHeading | pubmed-meshheading:12611061... | lld:pubmed |
| pubmed-article:12611061 | pubmed:meshHeading | pubmed-meshheading:12611061... | lld:pubmed |
| pubmed-article:12611061 | pubmed:meshHeading | pubmed-meshheading:12611061... | lld:pubmed |
| pubmed-article:12611061 | pubmed:meshHeading | pubmed-meshheading:12611061... | lld:pubmed |
| pubmed-article:12611061 | pubmed:meshHeading | pubmed-meshheading:12611061... | lld:pubmed |
| pubmed-article:12611061 | pubmed:meshHeading | pubmed-meshheading:12611061... | lld:pubmed |
| pubmed-article:12611061 | pubmed:meshHeading | pubmed-meshheading:12611061... | lld:pubmed |
| pubmed-article:12611061 | pubmed:meshHeading | pubmed-meshheading:12611061... | lld:pubmed |
| pubmed-article:12611061 | pubmed:meshHeading | pubmed-meshheading:12611061... | lld:pubmed |
| pubmed-article:12611061 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:12611061 | pubmed:articleTitle | Allogeneic hematopoietic cell transplantation for inborn metabolic diseases. | lld:pubmed |
| pubmed-article:12611061 | pubmed:affiliation | Departments of Medicine and Pediatrics, University of Pittsburgh Cancer Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, USA. | lld:pubmed |
| pubmed-article:12611061 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:12611061 | pubmed:publicationType | Review | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:12611061 | lld:pubmed |
