Mucopolysaccharidoses are characterized by the accumulation of undegraded glycosaminoglycans in lysosomes in multiple organs and by their excretion in high amounts in urine. The aim of this study is to determine if this simple, reliable and reproducible method is useful for the diagnosis of Mucopolysaccharidoses
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur to ma...
Deni Galileo, Ph.D. Shunji Tomatsu, MD, Ph.D.Mucopolysaccharidoses (MPS) are a group of lysosomal s...
Glycosaminoglycans (GAGs) are measured in urine to screen for mucopolysaccharidoses. Other assay pro...
Mucopolysaccharidoses are characterized by the accumulation of undegraded glycosaminoglycans in lyso...
The direct 1,9-dimethylmethyleneblue (DMB) method for quantifyingsulfatedglycosaminoglycan(GAG) in u...
A combination of anion-exchange chromatography and 30-40% gradient polyacrylamide gel electrophoresi...
A simple method is described for measurement of urinary glycosaminoglycans (GAG) in normal and patho...
Glycosaminoglycans in urine from patients representing the major different mucopolysaccharidoses wer...
The mucopolysaccharidoses are a family of genetic diseases involving faulty degradation of one or mo...
Mucopolysaccharidoses (MPS) are a group of inherited disorders caused by the defi ciency of specific...
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur, maki...
A technique for two-dimensional electrophoresis of urinary mucopolysaccharides (MPS) is described. T...
: Impaired glycosaminoglycans (GAGs) catabolism may lead to a cluster of rare metabolic and genetic ...
MPS-urine, urine sample from patient with mucopolysaccharido-sis; GAG, glycosaminoglycan; HSA, purif...
Diagnosis of the mucopolysaccharidoses (MPSs) generally relies on an initial analysis of total glyco...
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur to ma...
Deni Galileo, Ph.D. Shunji Tomatsu, MD, Ph.D.Mucopolysaccharidoses (MPS) are a group of lysosomal s...
Glycosaminoglycans (GAGs) are measured in urine to screen for mucopolysaccharidoses. Other assay pro...
Mucopolysaccharidoses are characterized by the accumulation of undegraded glycosaminoglycans in lyso...
The direct 1,9-dimethylmethyleneblue (DMB) method for quantifyingsulfatedglycosaminoglycan(GAG) in u...
A combination of anion-exchange chromatography and 30-40% gradient polyacrylamide gel electrophoresi...
A simple method is described for measurement of urinary glycosaminoglycans (GAG) in normal and patho...
Glycosaminoglycans in urine from patients representing the major different mucopolysaccharidoses wer...
The mucopolysaccharidoses are a family of genetic diseases involving faulty degradation of one or mo...
Mucopolysaccharidoses (MPS) are a group of inherited disorders caused by the defi ciency of specific...
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur, maki...
A technique for two-dimensional electrophoresis of urinary mucopolysaccharides (MPS) is described. T...
: Impaired glycosaminoglycans (GAGs) catabolism may lead to a cluster of rare metabolic and genetic ...
MPS-urine, urine sample from patient with mucopolysaccharido-sis; GAG, glycosaminoglycan; HSA, purif...
Diagnosis of the mucopolysaccharidoses (MPSs) generally relies on an initial analysis of total glyco...
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur to ma...
Deni Galileo, Ph.D. Shunji Tomatsu, MD, Ph.D.Mucopolysaccharidoses (MPS) are a group of lysosomal s...
Glycosaminoglycans (GAGs) are measured in urine to screen for mucopolysaccharidoses. Other assay pro...