BACKGROUND AND PURPOSE: Neuropathological examination in Friedreich ataxia (FRDA) reveals neuronal loss in the gray matter (GM) nuclei and degeneration of the white matter (WM) tracts in the spinal cord, brainstem and cerebellum, while the cerebral hemispheres are substantially spared. Tract-based spatial statistics (TBSS) enables an unbiased whole-brain quantitative analysis of the fractional anisotropy (FA) and mean diffusivity (MD) of the brain WM tracts in vivo. PATIENTS AND METHODS: We assessed with TBSS 14 patients with genetically confirmed FRDA and 14 age- and sex-matched healthy controls who were also examined with voxel-based morphometry (VBM) to assess regional atrophy of the GM and WM. RESULTS: TBSS revealed decreased FA in...
BACKGROUND AND PURPOSE: Imaging biomarkers of disease progression are desirable in inherited ataxias...
Background: Friedreich ataxia (FRDA) is the commonest form of autosomal recessive ataxia. This study...
BACKGROUND AND PURPOSE: Neurodegeneration in spinocerebellar ataxia type 1(SCA1) and 2(SCA2) is asso...
BACKGROUND AND PURPOSE: Neuropathological examination in Friedreich ataxia (FRDA) reveals neuronal ...
ABSTRACT Objective: Neuropathological descriptions of the brain in Friedreich’s ataxia (FRDA) were o...
Atrophy of the dentate nucleus is one of the major neuropathological changes in Friedreich ataxia (F...
Friedreich ataxia is a progressive neurodegenerative disorder with reported abnormalities in cerebel...
Objective: Friedreich ataxia (FRDA) is an inherited neurological disease defined by progressive move...
Friedreich ataxia is a progressive neurodegenerative disorder with reported abnormalities in cerebel...
OBJECTIVE: Neuropathological descriptions of the brain in Friedreich's ataxia (FRDA) were obtained b...
Friedreich's ataxia (FRDA) is a rare hereditary neurodegenerative disorder caused by a GAA repeat ex...
BACKGROUND AND PURPOSE: Imaging biomarkers of disease progression are desirable in inherited ataxias...
Background: Friedreich ataxia (FRDA) is the commonest form of autosomal recessive ataxia. This study...
BACKGROUND AND PURPOSE: Neurodegeneration in spinocerebellar ataxia type 1(SCA1) and 2(SCA2) is asso...
BACKGROUND AND PURPOSE: Neuropathological examination in Friedreich ataxia (FRDA) reveals neuronal ...
ABSTRACT Objective: Neuropathological descriptions of the brain in Friedreich’s ataxia (FRDA) were o...
Atrophy of the dentate nucleus is one of the major neuropathological changes in Friedreich ataxia (F...
Friedreich ataxia is a progressive neurodegenerative disorder with reported abnormalities in cerebel...
Objective: Friedreich ataxia (FRDA) is an inherited neurological disease defined by progressive move...
Friedreich ataxia is a progressive neurodegenerative disorder with reported abnormalities in cerebel...
OBJECTIVE: Neuropathological descriptions of the brain in Friedreich's ataxia (FRDA) were obtained b...
Friedreich's ataxia (FRDA) is a rare hereditary neurodegenerative disorder caused by a GAA repeat ex...
BACKGROUND AND PURPOSE: Imaging biomarkers of disease progression are desirable in inherited ataxias...
Background: Friedreich ataxia (FRDA) is the commonest form of autosomal recessive ataxia. This study...
BACKGROUND AND PURPOSE: Neurodegeneration in spinocerebellar ataxia type 1(SCA1) and 2(SCA2) is asso...