Quantitative assessment of brain stem and cerebellar atrophy in spinocerebellar ataxia types 3 and 6: impact on clinical status
L Eichler, B Bellenberg, HK Hahn… - American journal …, 2011 - Am Soc Neuroradiology
BACKGROUND AND PURPOSE: Cerebellar and brain stem atrophy are important features
in SCA3, whereas SCA6 has been regarded as a “pure” cerebellar disease. However …
in SCA3, whereas SCA6 has been regarded as a “pure” cerebellar disease. However …
Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6
JB Schulz, J Borkert, S Wolf, T Schmitz-Hübsch… - Neuroimage, 2010 - Elsevier
BACKGROUND AND OBJECTIVE: Biomarkers to monitor neurological dysfunction in
autosomal dominant inherited spinocerebellar ataxias (SCA) are lacking. We therefore …
autosomal dominant inherited spinocerebellar ataxias (SCA) are lacking. We therefore …
Spinocerebellar ataxia type 1: one-year longitudinal study to identify clinical and MRI measures of disease progression in patients and presymptomatic carriers
Abstract Spinocerebellar ataxias type 1 (SCA1) is an autosomal dominant disease usually
manifesting in adulthood. We performed a prospective 1-year longitudinal study in 14 …
manifesting in adulthood. We performed a prospective 1-year longitudinal study in 14 …
Gray and white matter alterations in spinocerebellar ataxia type 7: an in vivo DTI and VBM study
Spinocerebellar ataxia type 7 (SCA7) is a progressive neurodegenerative disorder
characterized by cerebellar ataxia and visual loss. It is caused by a CAG repeat expansion …
characterized by cerebellar ataxia and visual loss. It is caused by a CAG repeat expansion …
Brain atrophy measures in preclinical and manifest spinocerebellar ataxia type 2
K Reetz, R Rodríguez‐Labrada, I Dogan… - Annals of clinical …, 2018 - Wiley Online Library
Objective Spinocerebellar ataxia type 2 (SCA 2) is an autosomal dominantly inherited
neurodegenerative disease mainly affecting the cerebellum and brainstem. In this Cuban …
neurodegenerative disease mainly affecting the cerebellum and brainstem. In this Cuban …
[HTML][HTML] Progression of cerebellar atrophy in spinocerebellar ataxia type 2 gene carriers: a longitudinal MRI study in preclinical and early disease stages
Spinocerebellar ataxias type 2 (SCA2) is an autosomal dominant inherited disease caused
by expanded trinucleotide repeats (≥ 32 CAG) within the coding region of ATXN2 gene …
by expanded trinucleotide repeats (≥ 32 CAG) within the coding region of ATXN2 gene …
Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6
Spinocerebellar ataxias are dominantly inherited disorders that are associated with
progressive brain degeneration, mainly affecting the cerebellum and brainstem. As part of …
progressive brain degeneration, mainly affecting the cerebellum and brainstem. As part of …
Brain structural damage in spinocerebellar ataxia type 1: a VBM study
A Ginestroni, R Della Nave, C Tessa, M Giannelli… - Journal of …, 2008 - Springer
Background and objective Neuropathological description of the brain in spinocerebellar
ataxia type 1 (SCA1) is limited to a few cases. Voxel-based morphometry (VBM) enables an …
ataxia type 1 (SCA1) is limited to a few cases. Voxel-based morphometry (VBM) enables an …
Spinal cord atrophy in spinocerebellar ataxia type 3 and 6: impact on clinical disability
Objective To quantify spinal cord atrophy and its impact on clinical disability in
spinocerebellar ataxia (SCA) type 3 and 6. Methods Atrophy of the upper spinal cord was …
spinocerebellar ataxia (SCA) type 3 and 6. Methods Atrophy of the upper spinal cord was …
Dissociation of grey and white matter reduction in spinocerebellar ataxia type 3 and 6: a voxel-based morphometry study
C Lukas, L Schöls, B Bellenberg, U Rüb, H Przuntek… - Neuroscience …, 2006 - Elsevier
The aim of this study was to examine the different patterns of cerebellar and/or brainstem
atrophy in spinocerebellar ataxia (SCA) type 3 and 6. Eighteen patients (SCA3 n= 9, SCA6 …
atrophy in spinocerebellar ataxia (SCA) type 3 and 6. Eighteen patients (SCA3 n= 9, SCA6 …
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