[HTML][HTML] Management of essential tremor deep brain stimulation-induced side effects
AE Martinez-Nunez, FP Sarmento… - Frontiers in Human …, 2024 - frontiersin.org
Deep brain stimulation (DBS) is an effective surgical therapy for carefully selected patients
with medication refractory essential tremor (ET). The most popular anatomical targets for ET …
with medication refractory essential tremor (ET). The most popular anatomical targets for ET …
[HTML][HTML] Myelinating Glia: Potential Therapeutic Targets in Polyglutamine Spinocerebellar Ataxias
AF Putka, JP Mato, HS McLoughlin - Cells, 2023 - mdpi.com
Human studies, in combination with animal and cellular models, support glial cells as both
major contributors to neurodegenerative diseases and promising therapeutic targets. Among …
major contributors to neurodegenerative diseases and promising therapeutic targets. Among …
Brain structural abnormalities in the preclinical stage of Machado–Joseph disease/spinocerebellar ataxia type 3 (MJD/SCA3): evaluation by MRI morphometry …
M Li, X Chen, HL Xu, Z Huang, N Chen, Y Tu, S Gan… - Journal of …, 2022 - Springer
Objective To investigate whether neurite orientation dispersion and density imaging
(NODDI) could provide the added value for detecting brain microstructural alterations in the …
(NODDI) could provide the added value for detecting brain microstructural alterations in the …
Cognitive impairment and its neuroimaging correlates in spinocerebellar ataxia 2
Introduction Cognitive impairment (CI) is reported but is poorly explored in spinocerebellar
ataxia 2 (SCA2). This study was undertaken to evaluate and classify cognitive impairment in …
ataxia 2 (SCA2). This study was undertaken to evaluate and classify cognitive impairment in …
[HTML][HTML] Neuroradiological findings in GAA-FGF14 ataxia (SCA27B): more than cerebellar atrophy
S Chen, C Ashton, R Sakalla, G Clement, S Planel… - Medrxiv, 2024 - ncbi.nlm.nih.gov
Background GAA-FGF14 ataxia (SCA27B) is a recently reported late-onset ataxia caused by
a GAA repeat expansion in intron 1 of the FGF14 gene. Initial studies revealed cerebellar …
a GAA repeat expansion in intron 1 of the FGF14 gene. Initial studies revealed cerebellar …
[HTML][HTML] Cerebellar white matter abnormalities in Charcot–Marie–Tooth disease: a combined volumetry and diffusion tensor imaging analysis
Charcot–Marie–Tooth disease (CMT) is a genetically heterogeneous hereditary peripheral
neuropathy. Brain volumetry and diffusion tensor imaging (DTI) were performed in 47 …
neuropathy. Brain volumetry and diffusion tensor imaging (DTI) were performed in 47 …
Progressive white matter degeneration in patients with spinocerebellar ataxia type 2
Y Tu, Z Li, F Xiong, F Gao - Neuroradiology, 2024 - Springer
Purpose Spinocerebellar ataxia type 2 (SCA2) is a progressive neurodegenerative disorder
characterized by cerebellar atrophy. However, studies to elucidate the longitudinal …
characterized by cerebellar atrophy. However, studies to elucidate the longitudinal …
[HTML][HTML] A comprehensive review of iPS cell line-based disease modelling of the polyglutamine spinocerebellar ataxias 2 and 3: a focus on the research outcomes
N Raghunathan, S Sankaran… - Annals of Medicine and …, 2024 - journals.lww.com
Spinocerebellar ataxias (SCAs) are a rare autosomal dominant neurodegenerative disorder.
To date, approximately 50 different subtypes of SCAs have been characterized. The …
To date, approximately 50 different subtypes of SCAs have been characterized. The …
Biomarkers identification in spinocerebellar ataxias. Integrated functional evaluation of the cerebellum
G Coarelli - 2022 - theses.hal.science
Spinocerebellar ataxias (SCAs) are rare autosomal dominant neurodegenerative disorders
characterized by high heterogeneity regarding both their clinical manifestations and genetic …
characterized by high heterogeneity regarding both their clinical manifestations and genetic …