A technique for two-dimensional electrophoresis of urinary mucopolysaccharides (MPS) is described. The method allows differentiation of a number of mucopolysaccharidoses and is suitable for application in the routine laboratory. This technique should be used to evaluate urines from patients who have a positive MPS-spot test and/or an increased urinary excretion of MPS-bound uronic acid. Urinary MPS excretion patterns are given from normal individuals, patients with the Sanfilippo syndrome and the Hunter syndrome
A simple method is described for measurement of urinary glycosaminoglycans (GAG) in normal and patho...
textabstractIntroduction: Diagnosis of the mucopolysaccharidoses (MPSs) generally relies on an initi...
INTRODUCTION: Diagnosis of the mucopolysaccharidoses (MPSs) generally relies on an initial analysis ...
A technique for two-dimensional electrophoresis of urinary mucopolysaccharides (MPS) is described. T...
Mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders characterized by a ...
Mucopolysaccharidoses (MPS) are a group of inherited disorders caused by the defi ciency of specific...
Glycosaminoglycans in urine from patients representing the major different mucopolysaccharidoses wer...
Mucopolysaccharidoses are characterized by the accumulation of undegraded glycosaminoglycans in lyso...
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur to ma...
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur, maki...
Summary: A two dimensional electrophoretic method is described for the routine clinical analysis of ...
Mucopolysaccharidoses (MPS) is a disease of inborn errors of metabolism (IEM) and constitute a large...
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...
Background: The mucopolysaccharidosis (MPS) are a group of inherited metabolic disorders resulting f...
A simple method is described for measurement of urinary glycosaminoglycans (GAG) in normal and patho...
textabstractIntroduction: Diagnosis of the mucopolysaccharidoses (MPSs) generally relies on an initi...
INTRODUCTION: Diagnosis of the mucopolysaccharidoses (MPSs) generally relies on an initial analysis ...
A technique for two-dimensional electrophoresis of urinary mucopolysaccharides (MPS) is described. T...
Mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders characterized by a ...
Mucopolysaccharidoses (MPS) are a group of inherited disorders caused by the defi ciency of specific...
Glycosaminoglycans in urine from patients representing the major different mucopolysaccharidoses wer...
Mucopolysaccharidoses are characterized by the accumulation of undegraded glycosaminoglycans in lyso...
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur to ma...
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur, maki...
Summary: A two dimensional electrophoretic method is described for the routine clinical analysis of ...
Mucopolysaccharidoses (MPS) is a disease of inborn errors of metabolism (IEM) and constitute a large...
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...
Background: The mucopolysaccharidosis (MPS) are a group of inherited metabolic disorders resulting f...
A simple method is described for measurement of urinary glycosaminoglycans (GAG) in normal and patho...
textabstractIntroduction: Diagnosis of the mucopolysaccharidoses (MPSs) generally relies on an initi...
INTRODUCTION: Diagnosis of the mucopolysaccharidoses (MPSs) generally relies on an initial analysis ...