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Mucopolysaccharidosis II

Known as: MPS2, SIDS DEFICIENCY, Hunter's syndrome 
An X-linked, inherited lysosomal storage disease caused by the deficiency of the enzyme iduronate sulfatase that is responsible for the degradation… 
National Institutes of Health

Papers overview

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2010
2010
Tienda online donde Comprar An Introduction to Clinical Governance and Patient Safety al precio 65,90 € de Elizabeth Haxby… 
2005
2005
The aim of this project was to recover archaeological evidence of human parasite infection from the coastal shell middens of… 
2001
2001
Previous research has demonstrated impaired renal development, particularly with respect to glomerular number, in victims of… 
1996
1988
1988
To the Editor.— Mucopolysaccharidoses are a group of rare hereditary storage disorders characterized by various lysosomal… 
1987
1987
Substance P receptors were investigated in rat esophagus using 125I-Bolton-Hunter substance P as a labeling probe… 
Review
1983
Review
1983
Sudden infant death syndrome (SIDS) claims one in five hundred babies between 1 and 12 months of life. Since no cause of death is… 
1982
1982
Cardiac involvement of mucopolysaccharidosis has not been well characterized by echocardiography. In this paper, we reported a… 
1981
1981
Content, composition and molecular weight distribution of acidic glycosaminoglycans (GAGs) were determined in liver from five… 
1979
1979
We have examined several variables in the reagents and procedures used in the TSH radioreceptor assay, the binding of iodinated…