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EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood

European journal of neurology, 2014-04, Vol.21 (4), p.552-562

2014

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Olfactory bulb atrophy and caspase activation observed in the BACHD rat models of Huntington disease

Neurobiology of disease, 2019-05, Vol.125, p.219-231

2019

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A behavioral comparison of the common laboratory rat strains Lister Hooded, Lewis, Fischer 344 and Wistar in an automated homecage system

Genes, brain and behavior, 2014-03, Vol.13 (3), p.305-321

2014

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Behavioral and in vivo electrophysiological evidence for presymptomatic alteration of prefrontostriatal processing in the transgenic rat model for huntington disease

The Journal of neuroscience, 2011-06, Vol.31 (24), p.8986-8997

2011

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Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis

Lancet neurology, 2004-05, Vol.3 (5), p.291-304

2004

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14-3-3 proteins in the nervous system

Nature reviews. Neuroscience, 2003-09, Vol.4 (9), p.752-762

2003

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Involvement of alpha-synuclein in Parkinson's disease and other neurodegenerative disorders

Journal of Neural Transmission, 2000-01, Vol.107 (1), p.31-40

2000

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Mutation analysis of the seven in absentia homolog 1 (SIAH1) gene in Parkinson's disease

Journal of Neural Transmission, 2006-12, Vol.113 (12), p.1903-1908

2006

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Iron in neurodegenerative disorders

Neurotoxicity research, 2002-01, Vol.4 (7-8), p.637-653

2002

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The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodies

Journal of Neural Transmission, 2005-09, Vol.112 (9), p.1249-1254

2005

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Nuclear Localization of Ataxin-3 Is Required for the Manifestation of Symptoms in SCA3: In Vivo Evidence

The Journal of neuroscience, 2007-07, Vol.27 (28), p.7418-7428

2007

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Normal sensitivity to excitotoxicity in a transgenic Huntington's disease rat

Brain research bulletin, 2006-04, Vol.69 (3), p.306-310

2006

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Screening for mutations of the IRP2 gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra

Journal of Neural Transmission, 2004-04, Vol.111 (4), p.515-521

2004

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Disturbance of iron metabolism in Parkinson's disease -- ultrasonography as a biomarker

Neurotoxicity research, 2006-01, Vol.9 (1), p.1-13

2006

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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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Blood level of brain-derived neurotrophic factor mRNA is progressively reduced in rodent models of Huntington's disease: Restoration by the neuroprotective compound CEP-1347

Molecular and cellular neuroscience, 2008-09, Vol.39 (1), p.1-7

2008

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Protocol and Methodology of the Stroke in Young Fabry Patients (sifap1) Study: A Prospective Multicenter European Study of 5,024 Young Stroke Patients Aged 18–55 Years

Cerebrovascular diseases (Basel, Switzerland), 2011-01, Vol.31 (3), p.253-262

2011

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Behavioral deficits and striatal DA signaling in LRRK2 p.G2019S transgenic rats: a multimodal investigation including PET neuroimaging

Journal of Parkinson's disease, 2014, Vol.4 (3), p.483-498

2014

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Mutation analysis and association studies of the UCHL1 gene in German Parkinsonʼs disease patients

Neuroreport, 2000-07, Vol.11 (10), p.2079-2082

2000

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Genetic causes of Parkinson’s disease: extending the pathway

Journal of neural transmission. Supplementum, 2006 (70), p.181-189

2006

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Characterization of the rat spinocerebellar ataxia type 3 gene

Neurogenetics, 1997-11, Vol.1 (2), p.103-112

1997

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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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Screening for mutations in synaptotagmin XI in Parkinson's disease

Journal of neural transmission. Supplementum, 2004 (68), p.21

2004

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Cellular and subcellular localization of Huntingtin aggregates in the brain of a rat transgenic for Huntington disease

Journal of comparative neurology (1911), 2007-05, Vol.502 (3), p.483-483

2007

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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 (4), p.1167-1167

2005

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EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood

Olfactory bulb atrophy and caspase activation observed in the BACHD rat models of Huntington disease

A behavioral comparison of the common laboratory rat strains Lister Hooded, Lewis, Fischer 344 and Wistar in an automated homecage system

Behavioral and in vivo electrophysiological evidence for presymptomatic alteration of prefrontostriatal processing in the transgenic rat model for huntington disease

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis

14-3-3 proteins in the nervous system

Involvement of alpha-synuclein in Parkinson's disease and other neurodegenerative disorders

Mutation analysis of the seven in absentia homolog 1 (SIAH1) gene in Parkinson's disease

Iron in neurodegenerative disorders

The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodies

Nuclear Localization of Ataxin-3 Is Required for the Manifestation of Symptoms in SCA3: In Vivo Evidence

Normal sensitivity to excitotoxicity in a transgenic Huntington's disease rat

Screening for mutations of the IRP2 gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra

Disturbance of iron metabolism in Parkinson's disease -- ultrasonography as a biomarker

Specification of 14-3-3 proteins in Lewy bodies

Blood level of brain-derived neurotrophic factor mRNA is progressively reduced in rodent models of Huntington's disease: Restoration by the neuroprotective compound CEP-1347

Protocol and Methodology of the Stroke in Young Fabry Patients (sifap1) Study: A Prospective Multicenter European Study of 5,024 Young Stroke Patients Aged 18–55 Years

Behavioral deficits and striatal DA signaling in LRRK2 p.G2019S transgenic rats: a multimodal investigation including PET neuroimaging

Mutation analysis and association studies of the UCHL1 gene in German Parkinsonʼs disease patients

Genetic causes of Parkinson’s disease: extending the pathway

Characterization of the rat spinocerebellar ataxia type 3 gene

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

Screening for mutations in synaptotagmin XI in Parkinson's disease

Cellular and subcellular localization of Huntingtin aggregates in the brain of a rat transgenic for Huntington disease

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

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