17345556

Source:http://linkedlifedata.com/resource/pubmed/id/17345556

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008972, umls-concept:C0598391, umls-concept:C1739462
pubmed:dateCreated	2007-3-8
pubmed:abstractText	Important advances have been made in enzyme replacement therapy in the treatment of lysosomal diseases over the last two decades. Here we review the initial ERT trial using idursulfase in Hunter syndrome (mucopolysaccharidosis type II) and we also examine relevant aspects of the use of this enzyme.
pubmed:language	spa
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7706841
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Iduronate Sulfatase, http://linkedlifedata.com/resource/pubmed/chemical/idursulfase
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1576-6578
pubmed:author	pubmed-author:Gutiérrez-SolanaL GLG
pubmed:issnType	Electronic
pubmed:day	19
pubmed:volume	44 Suppl 1
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	S7-S11
pubmed:dateRevised	2009-5-28
pubmed:meshHeading	pubmed-meshheading:17345556-Adolescent, pubmed-meshheading:17345556-Adult, pubmed-meshheading:17345556-Child, pubmed-meshheading:17345556-Child, Preschool, pubmed-meshheading:17345556-Double-Blind Method, pubmed-meshheading:17345556-Humans, pubmed-meshheading:17345556-Iduronate Sulfatase, pubmed-meshheading:17345556-Mucopolysaccharidosis II
pubmed:year	2007
pubmed:articleTitle	[Clinical study of enzyme replacement therapy with idursulfase].
pubmed:affiliation	Hospital Infantil Universitario Nino Jesus, 28009 Madrid, Espana.
pubmed:publicationType	Journal Article, English Abstract, Randomized Controlled Trial, Clinical Trial, Phase II, Clinical Trial, Phase I