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Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias

Cerebellum (London, England), 2014-04, Vol.13 (2), p.269-302

2014

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Overexpression of human wildtype torsinA and human ΔGAG torsinA in a transgenic mouse model causes phenotypic abnormalities

Neurobiology of disease, 2007-08, Vol.27 (2), p.190-206

2007

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RNA interference of LRRK2–microarray expression analysis of a Parkinson’s disease key player

Neurogenetics, 2008-05, Vol.9 (2), p.83-94

2008

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Impaired olfactory bulb neurogenesis depends on the presence of human wild-type alpha-synuclein

Neuroscience, 2012-10, Vol.222, p.343-355

2012

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The aetiology of sporadic adult-onset ataxia

Brain (London, England : 1878), 2002-05, Vol.125 (5), p.961-968

2002

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Metabolic and Type 1 cannabinoid receptor imaging of a transgenic rat model in the early phase of Huntington disease

Experimental neurology, 2011-06, Vol.229 (2), p.440-449

2011

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Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia

Neurobiology of disease, 2010-05, Vol.38 (2), p.192-200

2010

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The natural history of degenerative ataxia : a retrospective study in 466 patients

Brain (London, England : 1878), 1998-04, Vol.121 (4), p.589-600

1998

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Microarray expression analysis reveals genetic pathways implicated in C621 synphilin-1-mediated toxicity

Journal of Neural Transmission, 2008-07, Vol.115 (7), p.941-958

2008

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Polymorphisms of the α-synuclein promoter: expression analyses and association studies in Parkinson's disease

Journal of Neural Transmission, 2003, Vol.110 (1), p.67-76

2003

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Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)

Annals of neurology, 2003-09, Vol.54 (3), p.367-375

2003

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Stem Cell Quiescence in the Hippocampal Neurogenic Niche Is Associated With Elevated Transforming Growth Factor-β Signaling in an Animal Model of Huntington Disease

Journal of neuropathology and experimental neurology, 2010-07, Vol.69 (7), p.717-728

2010

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Specification of 14-3-3 proteins in Lewy bodies

Annals of neurology, 2003-07, Vol.54 (1), p.135-135

2003

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Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?

Annals of neurology, 1997-12, Vol.42 (6), p.924-932

1997

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New mutations in protein kinase Cγ associated with spinocerebellar ataxia type 14

Annals of neurology, 2005-11, Vol.58 (5), p.720-729

2005

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Protein surveillance machinery in brains with spinocerebellar ataxia type 3: Redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusions

Annals of neurology, 2002-03, Vol.51 (3), p.302-310

2002

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Microarray expression analysis of gad mice implicates involvement of Parkinson's disease associated UCH-L1 in multiple metabolic pathways

Brain research. Molecular brain research., 2004-07, Vol.126 (1), p.88-97

2004

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Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation

Journal of neurochemistry, 2005-08, Vol.94 (3), p.639-650

2005

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Increased susceptibility to sporadic Parkinson's disease by a certain combined α-synuclein/apolipoprotein E genotype

Annals of neurology, 1999-05, Vol.45 (5), p.611-617

1999

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Adult neural precursor cells unaffected in animal models of DYT1 dystonia

Neuroreport, 2009-11, Vol.20 (17), p.1529-1533

2009

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Microarray expression analysis of human dopaminergic neuroblastoma cells after RNA interference of SNCA — A key player in the pathogenesis of Parkinson's disease

Brain research, 2009-02, Vol.1256, p.19-33

2009

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An Isoform of Ataxin-3 Accumulates in the Nucleus of Neuronal Cells in Affected Brain Regions of SCA3 Patients

Brain pathology (Zurich, Switzerland), 1998-10, Vol.8 (4), p.669-679

1998

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Do CTG expansions at the SCA8 locus cause ataxia?

Annals of neurology, 2003-07, Vol.54 (1), p.110-115

2003

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Analysis of the parkin deletion in sporadic and familial Parkinson's disease

Journal of Neural Transmission, 1999-03, Vol.106 (2), p.159-163

1999

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Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigra

Neuroscience letters, 2003-11, Vol.352 (1), p.53-56

2003

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Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias

Overexpression of human wildtype torsinA and human ΔGAG torsinA in a transgenic mouse model causes phenotypic abnormalities

RNA interference of LRRK2–microarray expression analysis of a Parkinson’s disease key player

Impaired olfactory bulb neurogenesis depends on the presence of human wild-type alpha-synuclein

The aetiology of sporadic adult-onset ataxia

Metabolic and Type 1 cannabinoid receptor imaging of a transgenic rat model in the early phase of Huntington disease

Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia

The natural history of degenerative ataxia : a retrospective study in 466 patients

Microarray expression analysis reveals genetic pathways implicated in C621 synphilin-1-mediated toxicity

Polymorphisms of the α-synuclein promoter: expression analyses and association studies in Parkinson's disease

Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)

Stem Cell Quiescence in the Hippocampal Neurogenic Niche Is Associated With Elevated Transforming Growth Factor-β Signaling in an Animal Model of Huntington Disease

Specification of 14-3-3 proteins in Lewy bodies

Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?

New mutations in protein kinase Cγ associated with spinocerebellar ataxia type 14

Protein surveillance machinery in brains with spinocerebellar ataxia type 3: Redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusions

Microarray expression analysis of gad mice implicates involvement of Parkinson's disease associated UCH-L1 in multiple metabolic pathways

Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation

Increased susceptibility to sporadic Parkinson's disease by a certain combined α-synuclein/apolipoprotein E genotype

Adult neural precursor cells unaffected in animal models of DYT1 dystonia

Microarray expression analysis of human dopaminergic neuroblastoma cells after RNA interference of SNCA — A key player in the pathogenesis of Parkinson's disease

An Isoform of Ataxin-3 Accumulates in the Nucleus of Neuronal Cells in Affected Brain Regions of SCA3 Patients

Do CTG expansions at the SCA8 locus cause ataxia?

Analysis of the parkin deletion in sporadic and familial Parkinson's disease

Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigra

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