Consensus paper: the cerebellum's role in movement and cognition
LF Koziol, D Budding, N Andreasen, S D'Arrigo… - The Cerebellum, 2014 - Springer
While the cerebellum's role in motor function is well recognized, the nature of its concurrent
role in cognitive function remains considerably less clear. The current consensus paper …
role in cognitive function remains considerably less clear. The current consensus paper …
Polyglutamine (PolyQ) diseases: genetics to treatments
HC Fan, LI Ho, CS Chi, SJ Chen, GS Peng… - Cell …, 2014 - journals.sagepub.com
The polyglutamine (polyQ) diseases are a group of neurodegenerative disorders caused by
expanded cytosine–adenine–guanine (CAG) repeats encoding a long polyQ tract in the …
expanded cytosine–adenine–guanine (CAG) repeats encoding a long polyQ tract in the …
Genetics of frontotemporal dementia
DA Olszewska, R Lonergan, EM Fallon… - Current neurology and …, 2016 - Springer
Frontotemporal dementia (FTD) is the second most common cause of dementia following
Alzheimer's disease (AD). Between 20 and 50% of cases are familial. Mutations in MAPT …
Alzheimer's disease (AD). Between 20 and 50% of cases are familial. Mutations in MAPT …
Evaluating the affective component of the cerebellar cognitive affective syndrome
U Wolf, MJ Rapoport… - The Journal of …, 2009 - Am Neuropsych Assoc
METHODS We conducted a systematic literature review looking at the affective component
of the cerebellar cognitive affective syndrome. We have included a wide array of emotion …
of the cerebellar cognitive affective syndrome. We have included a wide array of emotion …
Adaptation to visuomotor rotation and force field perturbation is correlated to different brain areas in patients with cerebellar degeneration
K Rabe, O Livne, ER Gizewski… - Journal of …, 2009 - journals.physiology.org
Although it is widely agreed that the cerebellum is necessary for learning and consolidation
of new motor tasks, it is not known whether adaptation to kinematic and dynamic errors is …
of new motor tasks, it is not known whether adaptation to kinematic and dynamic errors is …
[HTML][HTML] Digenic inheritance of STUB1 variants and TBP polyglutamine expansions explains the incomplete penetrance of SCA17 and SCA48
S Magri, L Nanetti, C Gellera, E Sarto, E Rizzo… - Genetics in …, 2022 - Elsevier
Purpose This study aimed to unravel the genetic factors underlying missing heritability in
spinocerebellar ataxia type 17 (SCA17) caused by polyglutamine-encoding CAG/CAA …
spinocerebellar ataxia type 17 (SCA17) caused by polyglutamine-encoding CAG/CAA …
Cerebellar ataxias
M Manto, D Marmolino - Current opinion in neurology, 2009 - journals.lww.com
Cerebellar ataxias : Current Opinion in Neurology Cerebellar ataxias : Current Opinion in
Neurology Log in or Register Subscribe to journalSubscribe Get new issue alertsGet alerts …
Neurology Log in or Register Subscribe to journalSubscribe Get new issue alertsGet alerts …
[HTML][HTML] Neuropsychiatric symptoms in spinocerebellar ataxias and Friedreich ataxia
S Karamazovova, V Matuskova, Z Ismail… - … & Biobehavioral Reviews, 2023 - Elsevier
Apart from its role in motor coordination, the importance of the cerebellum in cognitive and
affective processes has been recognized in the past few decades. Spinocerebellar ataxias …
affective processes has been recognized in the past few decades. Spinocerebellar ataxias …
Polyglutamine domain modulates the TBP-TFIIB interaction: implications for its normal function and neurodegeneration
MJ Friedman, AG Shah, ZH Fang, EG Ward… - Nature …, 2007 - nature.com
Expansion of the polyglutamine (polyQ) tract in human TATA-box binding protein (TBP)
causes the neurodegenerative disease spinocerebellar ataxia 17 (SCA17). It remains …
causes the neurodegenerative disease spinocerebellar ataxia 17 (SCA17). It remains …
Spinocerebellar ataxias
BW Soong, PJ Morrison - Handbook of clinical neurology, 2018 - Elsevier
There are over 40 autosomal dominant spinocerebellar ataxias (SCAs) now identified. In this
chapter we delineate the phenotypes of SCAs 1-44 and dentatorubral-pallidoluysian atrophy …
chapter we delineate the phenotypes of SCAs 1-44 and dentatorubral-pallidoluysian atrophy …