19117856

Source:http://linkedlifedata.com/resource/pubmed/id/19117856

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0001554, umls-concept:C0023786, umls-concept:C0087111, umls-concept:C0162791, umls-concept:C1273870
pubmed:issue	1
pubmed:dateCreated	2009-1-1
pubmed:abstractText	Disease management for mucopolysaccharidosis type I has been inconsistent because of disease rarity (approximately 1 case per 100,000 live births), phenotypic heterogeneity, and limited therapeutic options. The availability of hematopoietic stem cell transplantation and the recent introduction of enzyme replacement therapy for mucopolysaccharidosis I necessitate the establishment of system-specific management guidelines for this condition.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0376422
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	1098-4275
pubmed:author	pubmed-author:ClarkeLorne ALA, pubmed-author:International Consensus Panel on Management and Treatment of..., pubmed-author:MuenzerJosephJ, pubmed-author:WraithJames EJE
pubmed:issnType	Electronic
pubmed:volume	123
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	19-29
pubmed:meshHeading	pubmed-meshheading:19117856-Disease Management, pubmed-meshheading:19117856-Humans, pubmed-meshheading:19117856-Internationality, pubmed-meshheading:19117856-Mucopolysaccharidosis I, pubmed-meshheading:19117856-Treatment Outcome
pubmed:year	2009
pubmed:articleTitle	Mucopolysaccharidosis I: management and treatment guidelines.
pubmed:affiliation	Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA. muenzer@med.unc.edu
pubmed:publicationType	Journal Article, Practice Guideline