Fabry disease is a rare lysosomal storage disorder leading to cellular accumulation of globotriaosylceramide, especially in blood vessels. It is associated with severe early onset cerebrovascular disease and kidney and heart failure. The purpose of this study was to reveal possible disturbances in white matter integrity in Fabry disease patients using voxelwise diffusion-tensor imaging (DTI) analysis.Twelve Fabry disease patients, along with 13 healthy controls, underwent DTI and structural MRI. Voxel-based analysis of the DTI data was performed to assess possible differences in DTI parameters between Fabry disease patients and healthy controls. A selective region of interest analysis was performed for healthy volunteers and Fabry disease p...
BACKGROUND AND PURPOSE: Fabry disease (FD) is an inborn error of glycosphingolipid metabolism. To da...
Background and aim: It is unclear which patients with Fabry disease (FD) are at risk for progression...
Aim of the study was to evaluate the presence of Default Mode Network (DMN) modifications in Fabry D...
Fabry disease is a rare lysosomal storage disorder leading to cellular accumulation of globotriaosyl...
Fabry disease is a rare metabolic glycosphingolipid storage disease caused by deficiency of the lyso...
To assess structural and metabolic brain changes in subjects affected by Fabry disease (FD) or carry...
Introduction: Fabry disease (FD) is an X-linked lysosomal storage disorder resulting in vascular gly...
Abstract: Fabry disease (FD) is a rare X-linked disorder characterised by abnormal progressive lysos...
Cerebral white matter pathology is a common CNS manifestation of Fabry disease, visualized as white ...
Background: Fabry disease (FD) is a rare lysosomal storage disorder that might result in, amongst ot...
Background: Neurologic hallmarks of Fabry disease (FD) include small fiber neuropathy as well as cer...
Introduction: Fabry disease (FD) is a lysosomal storage disorder associated with marked cerebrovascu...
Introduction: Lysosomal storage disorders (LSD) are often characterized by abnormal brain developmen...
A high load of white matter lesions and enlarged basilar arteries have been shown in selected patien...
A high load of white matter lesions and enlarged basilar arteries have been shown in selected patien...
BACKGROUND AND PURPOSE: Fabry disease (FD) is an inborn error of glycosphingolipid metabolism. To da...
Background and aim: It is unclear which patients with Fabry disease (FD) are at risk for progression...
Aim of the study was to evaluate the presence of Default Mode Network (DMN) modifications in Fabry D...
Fabry disease is a rare lysosomal storage disorder leading to cellular accumulation of globotriaosyl...
Fabry disease is a rare metabolic glycosphingolipid storage disease caused by deficiency of the lyso...
To assess structural and metabolic brain changes in subjects affected by Fabry disease (FD) or carry...
Introduction: Fabry disease (FD) is an X-linked lysosomal storage disorder resulting in vascular gly...
Abstract: Fabry disease (FD) is a rare X-linked disorder characterised by abnormal progressive lysos...
Cerebral white matter pathology is a common CNS manifestation of Fabry disease, visualized as white ...
Background: Fabry disease (FD) is a rare lysosomal storage disorder that might result in, amongst ot...
Background: Neurologic hallmarks of Fabry disease (FD) include small fiber neuropathy as well as cer...
Introduction: Fabry disease (FD) is a lysosomal storage disorder associated with marked cerebrovascu...
Introduction: Lysosomal storage disorders (LSD) are often characterized by abnormal brain developmen...
A high load of white matter lesions and enlarged basilar arteries have been shown in selected patien...
A high load of white matter lesions and enlarged basilar arteries have been shown in selected patien...
BACKGROUND AND PURPOSE: Fabry disease (FD) is an inborn error of glycosphingolipid metabolism. To da...
Background and aim: It is unclear which patients with Fabry disease (FD) are at risk for progression...
Aim of the study was to evaluate the presence of Default Mode Network (DMN) modifications in Fabry D...