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Ewout Brunt

University Medical Center Groningen
University of Groningen

73

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4395

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Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.

2017 Brain
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Polyglutamine aggregation in Huntington's disease and spinocerebellar ataxia type 3: similar mechanisms in aggregate formation

2016 Neuropathology and Applied Neurobiology
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Polyglutamine aggregation in Huntington's disease and spinocerebellar ataxia type 3: similar mechanisms in aggregate formation: Polyglutamine aggregation in SCA3 and Huntington's disease

2016 Neuropathology and Applied Neurobiology
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No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra.

2015 Brain
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Huntington's Disease (HD)

2014 Brain Pathology
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Huntington's Disease (HD): Degeneration of Select Nuclei, Widespread Occurrence of Neuronal Nuclear and Axonal Inclusions in the Brainstem: The Brainstem in Huntington's Disease

2014 Brain Pathology
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Degeneration of the Cerebellum in Huntington's Disease (HD): Possible Relevance for the Clinical Picture and Potential Gateway to Pathological Mechanisms of the Disease Process

2013 Brain Pathology
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Degeneration of the cerebellum and brainstem in Huntington's disease (HD)

2013 Journal of the Neurological Sciences
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Involvement of the cholinergic basal forebrain nuclei in spinocerebellar ataxia type 2 (SCA2)

2013 Neuropathology and Applied Neurobiology
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Ataxin-2 Modulates the Levels of Grb2 and Src but Not Ras Signaling

2013 Journal of Molecular Neuroscience
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Citations (38)