Introduction: Lysosomal storage disorders (LSD) are often characterized by abnormal brain development, reflected by a reduction of intracranial volume (ICV). The aim of our study was to perform a volumetric analysis of intracranial tissues in Fabry Disease (FD), investigating possible reductions of ICV as a potential expression of abnormal brain development in this condition. Materials and Methods: Forty-two FD patients (15males,mean age 43.3±13.0 years) were enrolled along with 38 healthy controls (HC) of comparable age and sex. Volumetric MRI data were segmented using SPM12 to obtain intracranial tissue volumes, from which ICV values were derived. Results: Mean ICV of FD patients was 8.1% smaller compared to the control group (p<5·10−5)....
Introduction: Fabry disease (FD) is a lysosomal storage disorder associated with marked cerebrovascu...
Introduction: Aim of this study is to elucidate possible mechanisms of extrapyramidal damage in Fabr...
Objective: To explore the association between Enzyme Replacement Therapy (ERT), clinical characteris...
Introduction: Lysosomal storage disorders (LSD) are often characterized by abnormal brain developmen...
Introduction: Lysosomal storage disorders (LSD) are often characterized by abnormal brain developmen...
Introduction: Lysosomal storage disorders (LSD) are often characterized by abnormal brain developmen...
Fabry disease (FD) is an X-linked lysosomal storage disorder with multi-system involvement including...
To assess structural and metabolic brain changes in subjects affected by Fabry disease (FD) or carry...
Fabry disease is a rare lysosomal storage disorder leading to cellular accumulation of globotriaosyl...
Brain structural alterations and neuropsychiatric symptoms have been described repeatedly in Fabry d...
<div><p>Brain structural alterations and neuropsychiatric symptoms have been described repeatedly in...
Fabry disease is a rare metabolic glycosphingolipid storage disease caused by deficiency of the lyso...
Introduction: Fabry disease (FD) is an X-linked lysosomal storage disorder resulting in vascular gly...
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: Aim of this study is to elucidate possible mechanisms of extrapyramidal damage in Fabr...
Objective: To explore the association between Enzyme Replacement Therapy (ERT), clinical characteris...
Introduction: Lysosomal storage disorders (LSD) are often characterized by abnormal brain developmen...
Introduction: Lysosomal storage disorders (LSD) are often characterized by abnormal brain developmen...
Introduction: Lysosomal storage disorders (LSD) are often characterized by abnormal brain developmen...
Fabry disease (FD) is an X-linked lysosomal storage disorder with multi-system involvement including...
To assess structural and metabolic brain changes in subjects affected by Fabry disease (FD) or carry...
Fabry disease is a rare lysosomal storage disorder leading to cellular accumulation of globotriaosyl...
Brain structural alterations and neuropsychiatric symptoms have been described repeatedly in Fabry d...
<div><p>Brain structural alterations and neuropsychiatric symptoms have been described repeatedly in...
Fabry disease is a rare metabolic glycosphingolipid storage disease caused by deficiency of the lyso...
Introduction: Fabry disease (FD) is an X-linked lysosomal storage disorder resulting in vascular gly...
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: Aim of this study is to elucidate possible mechanisms of extrapyramidal damage in Fabr...
Objective: To explore the association between Enzyme Replacement Therapy (ERT), clinical characteris...