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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2011-2-4
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pubmed:abstractText |
To use the Hunter Outcome Survey, an international database, to assess the safety and effectiveness of enzyme replacement therapy with idursulfase in patients with Hunter syndrome who started treatment before 6 years of age.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1530-0366
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
102-9
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pubmed:meshHeading |
pubmed-meshheading:21233716-Adolescent,
pubmed-meshheading:21233716-Adult,
pubmed-meshheading:21233716-Child,
pubmed-meshheading:21233716-Child, Preschool,
pubmed-meshheading:21233716-Clinical Trials as Topic,
pubmed-meshheading:21233716-Data Collection,
pubmed-meshheading:21233716-Databases, Factual,
pubmed-meshheading:21233716-Enzyme Replacement Therapy,
pubmed-meshheading:21233716-Glycosaminoglycans,
pubmed-meshheading:21233716-Humans,
pubmed-meshheading:21233716-Iduronate Sulfatase,
pubmed-meshheading:21233716-Infant,
pubmed-meshheading:21233716-Infusions, Intravenous,
pubmed-meshheading:21233716-Mucopolysaccharidosis II,
pubmed-meshheading:21233716-Treatment Outcome,
pubmed-meshheading:21233716-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
Idursulfase treatment of Hunter syndrome in children younger than 6 years: results from the Hunter Outcome Survey.
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pubmed:affiliation |
Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. muenzer@med.unc.edu
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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