Results 171 to 180 of about 27,164 (223)

Associations between CAG repeat size, brain and spinal cord volume loss, and motor symptoms in spinocerebellar ataxia type 3: a cohort study. [PDF]

open access: yesOrphanet J Rare Dis
Ye ZX   +13 more
europepmc   +1 more source

Compressed cerebellar functional connectome hierarchy in spinocerebellar ataxia type 3. [PDF]

open access: yesHum Brain Mapp
Liu X   +9 more
europepmc   +1 more source

Exploring functional and structural connectivity disruptions in spinocerebellar ataxia type 3: Insights from gradient analysis. [PDF]

open access: yesCNS Neurosci Ther
Wang X   +11 more
europepmc   +1 more source

The volume of the subthalamic nucleus in spinocerebellar ataxia type 3: potential relevance for the clinical phenotype and treatment of parkinsonian symptoms with deep brain stimulation. [PDF]

open access: yesJ Neurol
Minnerop M   +13 more
europepmc   +1 more source

Progression of biological markers in spinocerebellar ataxia type 3: analysis of longitudinal data from the ESMI cohort

open access: yes
Berger M   +51 more
europepmc   +1 more source

Phonoarticulation in spinocerebellar ataxia type 3

European Archives of Oto-Rhino-Laryngology, 2016
Phonoarticulation is characterized by changes in resonance, diadochokinesis, prosody, sound frequency, vocal quality, and intraoral pressure. The main aim of this study was to characterize the phonoarticulation in spinocerebellar ataxia type 3 (SCA3) and correlate it with clinical and genetic factors. Thirty-one patients with SCA3 who were subjected to
A E, Wolf   +4 more
openaire   +2 more sources

Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes

open access: yesBrain, 2014
Polyglutamine-coding (CAG)n repeat expansions in seven different genes cause spinocerebellar ataxias. Although the size of the expansion is negatively correlated with age at onset, it accounts for only 50-70% of its variability.
Sophie Tezenas Du Montcel   +2 more
exaly   +2 more sources

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