Mucopolysaccharidosis Type IIIA

Known as: Mucopolysaccharidosis Type IIIAs, Sanfilippo Syndrome A, MPS 3 A 
A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme heparan sulfate sulfatase. It is characterized by behavioral… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1972-2017
051019722017

Papers overview

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2016
2016
OBJECTIVES To characterize the clinical course of mucopolysaccharidosis type IIIA (MPS IIIA), and identify potential endpoints… (More)
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2014
2014
OBJECTIVES To assess autism spectrum disorder (ASD) behaviors in children with mucopolysaccharidosis type IIIA (MPS IIIA) using a… (More)
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2013
2013
For most lysosomal storage diseases (LSDs) affecting the CNS, there is currently no cure. The BBB, which limits the… (More)
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2010
2010
OBJECTIVE Mucopolysaccharidosis (MPS) IIIA (Sanfilippo syndrome type A) is a lysosomal storage disorder caused by deficiency of… (More)
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2008
2008
Mucopolysaccharidosis (MPS) IIIA, or Sanfilippo syndrome, is a lysosomal storage disorder characterized by severe and progressive… (More)
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2008
2008
Mucopolysaccharidosis type IIIA (MPS IIIA) is a heritable glycosaminoglycan (GAG) storage disorder which is characterised by… (More)
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2007
2007
BACKGROUND Mucopolysaccharidosis type IIIA (MPS IIIA) is the most common of the mucopolysaccharidoses. The disease is caused by a… (More)
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2006
2006
Reduction of an enzyme activity required for the lysosomal degradation of glycosaminoglycan (gag) chains will result in a… (More)
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2006
2006
The original mucopolysaccharidosis type IIIA (MPS IIIA) mice were identified in a mixed background with contributions from four… (More)
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2004
2004
Mucopolysaccharidosis type IIIA (MPS IIIA; Sanfilippo syndrome) is a lysosomal storage disorder characterized by severe CNS… (More)
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