Mucopolysaccharidoses (MPSs) are a group of inherited disorders due to lysosomal enzyme deficiencies which lead to multi-organ accumulation of glycosaminoglycans. Some forms of MPS disorders are characterized by various degrees of mental retardation. Magnetic Resonance Imaging (MRI) is the primary imaging technique to detect CNS alterations. The aim of this study is to evaluate the correlation between white matter (WM) alterations and the presence of mental retardation. We analyzed 20 patients with different forms of MPSs, 11 with mental retardation and 9 with a normal cognitive function; all of them underwent brain MRI and received a score on the basis of the alterations (WM alterations; perivascular, subarachnoid, and ventricular space en...
Mucopolysaccharidoses (MPS) are characterized by mental retardation constantly present in the severe...
ABSTRACT- We re p o rt results of a magnetic ressonance imaging (MRI) study of 146 Brazilian childre...
AbstractShwachman–Diamond syndrome is a rare recessive genetic disease caused by mutations in SBDS g...
Mucopolysaccharidoses (MPSs) are a group of inherited disorders due to lysosomal enzyme deficiencies...
Objective: To advance the prediction of the neurocognitive development in MPS II patients by jointly...
BACKGROUND AND PURPOSE: There are no reliable markers to predict neurologic outcome of patients with...
Introduction: Mucopolysaccharidoses (MPS) are a group of inherited disorders due to lysosomal enzyme...
Mucopolysaccharidosis (MPS) disorders are caused by deficiencies in lysosomal enzymes, leading to im...
Mucopolysaccharidoses (MPS) are characterized by mental retardation constantly present in the severe...
Mucopolysaccharidoses (MPS) are the group of lysosomal storage disorders caused by deficiencies of e...
Mucopolysaccharidoses (MPS) are the group of lysosomal storage disorders caused by deficiencies of e...
UnlabelledThe phenotype of attenuated mucopolysaccharidosis type II (MPS II), also called Hunter syn...
Abstract Mucopolysaccharidoses (MPS) are a group of lysosomal multisystemic, chronic, and progressiv...
ObjectivePrevious research suggests attention and white matter (WM) abnormalities in individuals wit...
m of this study was to evaluate the frequency of callosal abnormalities and white matter alterations...
Mucopolysaccharidoses (MPS) are characterized by mental retardation constantly present in the severe...
ABSTRACT- We re p o rt results of a magnetic ressonance imaging (MRI) study of 146 Brazilian childre...
AbstractShwachman–Diamond syndrome is a rare recessive genetic disease caused by mutations in SBDS g...
Mucopolysaccharidoses (MPSs) are a group of inherited disorders due to lysosomal enzyme deficiencies...
Objective: To advance the prediction of the neurocognitive development in MPS II patients by jointly...
BACKGROUND AND PURPOSE: There are no reliable markers to predict neurologic outcome of patients with...
Introduction: Mucopolysaccharidoses (MPS) are a group of inherited disorders due to lysosomal enzyme...
Mucopolysaccharidosis (MPS) disorders are caused by deficiencies in lysosomal enzymes, leading to im...
Mucopolysaccharidoses (MPS) are characterized by mental retardation constantly present in the severe...
Mucopolysaccharidoses (MPS) are the group of lysosomal storage disorders caused by deficiencies of e...
Mucopolysaccharidoses (MPS) are the group of lysosomal storage disorders caused by deficiencies of e...
UnlabelledThe phenotype of attenuated mucopolysaccharidosis type II (MPS II), also called Hunter syn...
Abstract Mucopolysaccharidoses (MPS) are a group of lysosomal multisystemic, chronic, and progressiv...
ObjectivePrevious research suggests attention and white matter (WM) abnormalities in individuals wit...
m of this study was to evaluate the frequency of callosal abnormalities and white matter alterations...
Mucopolysaccharidoses (MPS) are characterized by mental retardation constantly present in the severe...
ABSTRACT- We re p o rt results of a magnetic ressonance imaging (MRI) study of 146 Brazilian childre...
AbstractShwachman–Diamond syndrome is a rare recessive genetic disease caused by mutations in SBDS g...