Cataloged from PDF version of article.PURPOSE We aimed to investigate white matter diffusivity abnormalities in hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) patients in relation with electrophysiological findings. MATERIALS AND METHODS Brain magnetic resonance imaging (MRI) and diffusion tensor imaging were performed on four HSP-TCC patients and 15 age-matched healthy subjects. Voxel-wise statistical analysis of fractional anisotropy, axial diffusivity, radial diffusivity, and mean diffusivity maps were carried out using tract-based spatial statistics, and significantly affected voxels were labeled using a human white matter atlas. Conventional nerve conduction studies, cortical and spinal-root motor evoked potentials, ...
BACKGROUND AND PURPOSE: Extension and characteristics of WM involvement other than the brain stem re...
Hereditary spastic paraparesis (HSP) is a heterogeneous group of neurodegenerative disorders with pr...
Mutations in the SPG4 gene (SPG4-HSP) are the most frequent cause of hereditary spastic paraplegia, ...
PURPOSEWe aimed to investigate white matter diffusivity abnormalities in hereditary spastic parapleg...
PURPOSE We aimed to investigate white matter diffusivity abnormalities in hereditary spastic paraple...
Objective: To identify structural white matter alterations in patients with pure hereditary spastic ...
Background: Mutations in SPG11 are the most frequent known cause of autosomal recessive hereditary s...
BACKGROUND AND PURPOSE: The hereditary spastic paraplegias are a group of genetically heterogeneous ...
Our objective was to estimate the frequency as well as to establish the clinical and neuroimaging pr...
Background: Hereditary spastic paraplegias (HSP) are a composite and genetically heterogeneous group...
Mutations in SPG11 are the most frequent known cause of autosomal recessive hereditary spastic parap...
BACKGROUND AND PURPOSE: Many studies have observed atrophy and abnormal diffusion within the CC in M...
INTRODUCTION: The neural tracts responsible for gross motor dysfunction in children with spastic cer...
Although often clinically indistinguishable in the early stages, Parkinson's disease (PD), Multiple ...
<div><p>Mutations in the <i>SPG4</i> gene (SPG4-HSP) are the most frequent cause of hereditary spast...
BACKGROUND AND PURPOSE: Extension and characteristics of WM involvement other than the brain stem re...
Hereditary spastic paraparesis (HSP) is a heterogeneous group of neurodegenerative disorders with pr...
Mutations in the SPG4 gene (SPG4-HSP) are the most frequent cause of hereditary spastic paraplegia, ...
PURPOSEWe aimed to investigate white matter diffusivity abnormalities in hereditary spastic parapleg...
PURPOSE We aimed to investigate white matter diffusivity abnormalities in hereditary spastic paraple...
Objective: To identify structural white matter alterations in patients with pure hereditary spastic ...
Background: Mutations in SPG11 are the most frequent known cause of autosomal recessive hereditary s...
BACKGROUND AND PURPOSE: The hereditary spastic paraplegias are a group of genetically heterogeneous ...
Our objective was to estimate the frequency as well as to establish the clinical and neuroimaging pr...
Background: Hereditary spastic paraplegias (HSP) are a composite and genetically heterogeneous group...
Mutations in SPG11 are the most frequent known cause of autosomal recessive hereditary spastic parap...
BACKGROUND AND PURPOSE: Many studies have observed atrophy and abnormal diffusion within the CC in M...
INTRODUCTION: The neural tracts responsible for gross motor dysfunction in children with spastic cer...
Although often clinically indistinguishable in the early stages, Parkinson's disease (PD), Multiple ...
<div><p>Mutations in the <i>SPG4</i> gene (SPG4-HSP) are the most frequent cause of hereditary spast...
BACKGROUND AND PURPOSE: Extension and characteristics of WM involvement other than the brain stem re...
Hereditary spastic paraparesis (HSP) is a heterogeneous group of neurodegenerative disorders with pr...
Mutations in the SPG4 gene (SPG4-HSP) are the most frequent cause of hereditary spastic paraplegia, ...