Add to ORKGMucopolysaccharidoses (MPS) is a disease of inborn errors of metabolism (IEM) and constitute a large and heterogenous subgroup among the lysosomal storage diseases
The mucopolysaccharidoses (MPSs) are a group of 11 distinct metabolic disorders that result from the...
Background: The mucopolysaccharidosis (MPS) are a group of inherited metabolic disorders resulting f...
Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is an autosomal recessive lysosomal storage ...
i11troductio11: Mucopolysaccharidoses (MPS) is a disease of inborn errors of metabolism (!EM). It co...
Mucopolysaccharidoses (MPS) are a group of inherited disorders caused by the defi ciency of specific...
Mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders characterized by a ...
Introduction: Mucopolysaccharidoses (MPS) are a group of inherited disorders caused by the deficienc...
Mucopolysaccharidoses (MPS) constitute, owing to their biochemical, genetical and clinical character...
Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases (LSDs) caused by an inherited...
The absent of a referral centre for mucopolysaccharidosis (MPS) in Malaysia is a major problem in d...
A technique for two-dimensional electrophoresis of urinary mucopolysaccharides (MPS) is described. T...
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur, maki...
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur to ma...
: Impaired glycosaminoglycans (GAGs) catabolism may lead to a cluster of rare metabolic and genetic ...
After the first description of a patient recognized as a MPS case was made in 1917, several similar ...
The mucopolysaccharidoses (MPSs) are a group of 11 distinct metabolic disorders that result from the...
Background: The mucopolysaccharidosis (MPS) are a group of inherited metabolic disorders resulting f...
Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is an autosomal recessive lysosomal storage ...
i11troductio11: Mucopolysaccharidoses (MPS) is a disease of inborn errors of metabolism (!EM). It co...
Mucopolysaccharidoses (MPS) are a group of inherited disorders caused by the defi ciency of specific...
Mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders characterized by a ...
Introduction: Mucopolysaccharidoses (MPS) are a group of inherited disorders caused by the deficienc...
Mucopolysaccharidoses (MPS) constitute, owing to their biochemical, genetical and clinical character...
Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases (LSDs) caused by an inherited...
The absent of a referral centre for mucopolysaccharidosis (MPS) in Malaysia is a major problem in d...
A technique for two-dimensional electrophoresis of urinary mucopolysaccharides (MPS) is described. T...
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur, maki...
Mucopolysaccharidoses (MPS) diagnosis is often delayed and irreversible organ damage can occur to ma...
: Impaired glycosaminoglycans (GAGs) catabolism may lead to a cluster of rare metabolic and genetic ...
After the first description of a patient recognized as a MPS case was made in 1917, several similar ...
The mucopolysaccharidoses (MPSs) are a group of 11 distinct metabolic disorders that result from the...
Background: The mucopolysaccharidosis (MPS) are a group of inherited metabolic disorders resulting f...
Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is an autosomal recessive lysosomal storage ...