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rdf:type |
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|
lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2001-4-23
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pubmed:abstractText |
The mucopolysaccharidoses (MPS) are a heterogeneous group of inborn errors of lysosomal glycosaminoglycan (GAG) metabolism. The importance of this group of disorders among the inborn errors of metabolism led us to report 19 cases.
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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:issn |
0041-8781
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pubmed:author |
pubmed-author:AlbanoL MLM,
pubmed-author:AndradeC ECE,
pubmed-author:BertolaD RDR,
pubmed-author:BurinMM,
pubmed-author:ChongA KAK,
pubmed-author:CoelhoJJ,
pubmed-author:GiuglianiRR,
pubmed-author:LeistnerSS,
pubmed-author:NaderH BHB,
pubmed-author:PuppeBB,
pubmed-author:SugayamaS SSS,
pubmed-author:TomaLL,
pubmed-author:UtagawaC YCY
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pubmed:issnType |
Print
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pubmed:volume |
55
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
213-8
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:11313661-Adolescent,
pubmed-meshheading:11313661-Adult,
pubmed-meshheading:11313661-Child,
pubmed-meshheading:11313661-Child, Preschool,
pubmed-meshheading:11313661-Female,
pubmed-meshheading:11313661-Glycosaminoglycans,
pubmed-meshheading:11313661-Humans,
pubmed-meshheading:11313661-Male,
pubmed-meshheading:11313661-Mucopolysaccharidoses,
pubmed-meshheading:11313661-Mucopolysaccharidosis VI,
pubmed-meshheading:11313661-Phenotype
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pubmed:articleTitle |
Clinical and laboratorial study of 19 cases of mucopolysaccharidoses.
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pubmed:affiliation |
Genetic Unit of the Department of Pediatrics, Hospital das Clinicas, University of São Paulo.
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pubmed:publicationType |
Journal Article
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