Dried blood spot (DBS) technology is a cheap and easy method largely applied in newborn screening. Mucopolysaccharidoses (MPS) are characterized by the deficit of enzymes that degrade glycosaminoglycans (GAGs) characterized by progressive worsening of the conditions. For a possible early diagnosis of MPS, we developed a method of uronic acid (UA)-GAGs determination in DBS of 600 healthy newborns and from a small group of MPS subjects matched for age. Spotted blood UA-GAGs of the normal newborns are composed of 67.2% chondroitin sulfate (CS), 28.6% heparan sulfate (HS) and 4.4% hyaluronic acid with a CS/HS ratio of 2.35 and a total GAGs content of 0.43 μg/DBS. A chemical evaluation of CS and HS structure was performed by measuring their disa...
Glycosaminoglycans (GAGs) are present in proteoglycans, which play critical physiological roles in v...
Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases (LSDs) caused by an inherited...
Abstract Background Mucopolysaccharidoses (MPS) are lysosomal storage diseases in which mutations of...
Dried blood spot (DBS) technology is a cheap and easy method largely applied in newborn screening. M...
Background Mucopolysaccharidoses (MPS) are a group of inborn errors of metabolism that are progressi...
BACKGROUND: Urine are easily accessible and relatively simple to process and uronic acid-bearing g...
Mucopolysaccharidosis type I (MPS I) was added to our expanded screening panel in 2015. Since then, ...
All newborn screening (NBS) for mucopolysaccharidosis-I and -II (MPS-I and MPS-II) is carried out vi...
Backgroung In this study, we propose a high-throughput procedure for the simultaneous determinatio...
The mucopolysaccharidoses (MPS) result from attenuation or loss of enzyme activities required for ly...
Urine are easily accessible and relatively simple to process and uronic acid-bearing glycosaminoglyc...
Abstract Objectives Mucopolysaccharidosis type I...
Thesis (Ph.D.)--University of Washington, 2018Chapter I. Development of Newborn Screening Method for...
The mucopolysaccharidoses are a family of genetic diseases involving faulty degradation of one or mo...
Backgroung In this study, we propose a high-throughput procedure for the simultaneous determinatio...
Glycosaminoglycans (GAGs) are present in proteoglycans, which play critical physiological roles in v...
Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases (LSDs) caused by an inherited...
Abstract Background Mucopolysaccharidoses (MPS) are lysosomal storage diseases in which mutations of...
Dried blood spot (DBS) technology is a cheap and easy method largely applied in newborn screening. M...
Background Mucopolysaccharidoses (MPS) are a group of inborn errors of metabolism that are progressi...
BACKGROUND: Urine are easily accessible and relatively simple to process and uronic acid-bearing g...
Mucopolysaccharidosis type I (MPS I) was added to our expanded screening panel in 2015. Since then, ...
All newborn screening (NBS) for mucopolysaccharidosis-I and -II (MPS-I and MPS-II) is carried out vi...
Backgroung In this study, we propose a high-throughput procedure for the simultaneous determinatio...
The mucopolysaccharidoses (MPS) result from attenuation or loss of enzyme activities required for ly...
Urine are easily accessible and relatively simple to process and uronic acid-bearing glycosaminoglyc...
Abstract Objectives Mucopolysaccharidosis type I...
Thesis (Ph.D.)--University of Washington, 2018Chapter I. Development of Newborn Screening Method for...
The mucopolysaccharidoses are a family of genetic diseases involving faulty degradation of one or mo...
Backgroung In this study, we propose a high-throughput procedure for the simultaneous determinatio...
Glycosaminoglycans (GAGs) are present in proteoglycans, which play critical physiological roles in v...
Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases (LSDs) caused by an inherited...
Abstract Background Mucopolysaccharidoses (MPS) are lysosomal storage diseases in which mutations of...