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Mutant COQ2 in Multiple-System Atrophy

The New England journal of medicine, 2014-07, Vol.371 (1), p.80-83

2014

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Lack of Nigral Pathology in Transgenic Mice Expressing Human α-Synuclein Driven by the Tyrosine Hydroxylase Promoter

Neurobiology of disease, 2001-06, Vol.8 (3), p.535-539

2001

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NEUROGENETICS: A GUIDE FOR CLINICIANS. 2012. Edited by Nicholas W. Wood. Published by Cambridge University Press. 241 pages. C$70.00 approx

Canadian journal of neurological sciences, 2013-11, Vol.40 (6), p.903-903

Farrer, Matt

2013

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NEUROGENETICS: A GUIDE FOR CLINICIANS. 2012. Edited byWood Nicholas W.. Published by Cambridge University Press. 241 pages. C$70.00 approx

Canadian journal of neurological sciences, 2013-11, Vol.40 (6), p.903

Farrer, Matt

2013

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Low frequency of pathogenic mutations in the ubiquitin carboxyterminal hydrolase gene in familial Parkinsonʼs disease

Neuroreport, 1999-02, Vol.10 (2), p.427-429

1999

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Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium

Neurology, 2022-08, Vol.99 (7)

2022

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α-Synuclein Repeat Polymorphisms and Pesticide Exposure in Parkinsonʼs Disease

Epidemiology (Cambridge, Mass.), 2009-11, Vol.20, p.S124

2009

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A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1

Nature medicine, 1998-04, Vol.4 (4), p.452-455

1998

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Mutant COQ2 in multiple-system atrophy

The New England journal of medicine, 2014-07, Vol.371 (1), p.80

2014

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Tau neurotoxicity without the lesions: a fly challenges a tangled web

Trends in neurosciences (Regular ed.), 2002-07, Vol.25 (7), p.327-329

2002

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[alpha]-Synuclein Gene May Interact with Environmental Factors in Increasing Risk of Parkinson's Disease

Neuroepidemiology, 2010-10, Vol.35 (3), p.191-195

2010

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P1-106: LRRK2 as a common link between tauopathies and synucleinopathies

Alzheimer's & dementia, 2008-07, Vol.4 (4), p.T237-T238

2008

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P4-158 Tau H1 haplotype disease association and splice mutations: investigations into mutational mechanisms

Neurobiology of aging, 2004-07, Vol.25, p.S520-S520

2004

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A family with a tau P301L mutation presenting with parkinsonism

Parkinsonism & related disorders, 2002-12, Vol.9 (2), p.121-123

2002

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Clinical, 18 F‐dopa PET, and genetic analysis of an ethnic Chinese kindred with early‐onset parkinsonism and parkin gene mutations

Movement disorders, 2002-07, Vol.17 (4), p.670-675

2002

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Lack of Nigral Pathology in Transgenic Mice Expressing Human a-Synuclein Driven by the Tyrosine Hydroxylase Promoter

Neurobiology of disease, 2001-06, Vol.8 (3), p.535-539

2001

Volltextzugriff (PDF)

NEUROGENETICS: A GUIDE FOR CLINICIANS. 2012. Edited by WoodNicholas W.. Published by Cambridge University Press. 241 pages. C$70.00 approx

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 2013, Vol.40 (6), p.903-903

Farrer, Matt

2013

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Accurate determination of ataxin-2 polyglutamine expansion in patients with intermediate-range repeats

Genetic testing, 2002, Vol.6 (3), p.217-220

2002

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Strain and temperature dependent aggregation of Candida auris is attenuated by inhibition of surface amyloid proteins

Cell surface (Amsterdam), 2023-12, Vol.10, p.100110-100110, Article 100110

2023

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Weekend specialist intensity and admission mortality in acute hospital trusts in England: a cross-sectional study

The Lancet (British edition), 2016-07, Vol.388 (10040), p.178-186

2016

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Dynamic aberrometer/topographer designed for clinical measurement and treatment of highly aberrated eyes

Optical engineering, 2022-12, Vol.61 (12)

2022

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Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions

Acta neuropathologica, 2007-05, Vol.113 (5), p.601-606

2007

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Management of Obstructive Sleep Apnea: An Evidence-Based, Multidisciplinary Textbook

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Leg Ulcers in Sickle Cell Anemia Are Associated with Laboratory Markers of Hemolysis and SNPs in KL and Genes of the TGF-β/BMP Pathway

Blood, 2005-11, Vol.106 (11), p.2317-2317

2005

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Mutant COQ2 in Multiple-System Atrophy

Lack of Nigral Pathology in Transgenic Mice Expressing Human α-Synuclein Driven by the Tyrosine Hydroxylase Promoter

NEUROGENETICS: A GUIDE FOR CLINICIANS. 2012. Edited by Nicholas W. Wood. Published by Cambridge University Press. 241 pages. C$70.00 approx

NEUROGENETICS: A GUIDE FOR CLINICIANS. 2012. Edited byWood Nicholas W.. Published by Cambridge University Press. 241 pages. C$70.00 approx

Low frequency of pathogenic mutations in the ubiquitin carboxyterminal hydrolase gene in familial Parkinsonʼs disease

Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium

α-Synuclein Repeat Polymorphisms and Pesticide Exposure in Parkinsonʼs Disease

A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1

Mutant COQ2 in multiple-system atrophy

Tau neurotoxicity without the lesions: a fly challenges a tangled web

[alpha]-Synuclein Gene May Interact with Environmental Factors in Increasing Risk of Parkinson's Disease

P1-106: LRRK2 as a common link between tauopathies and synucleinopathies

P4-158 Tau H1 haplotype disease association and splice mutations: investigations into mutational mechanisms

A family with a tau P301L mutation presenting with parkinsonism

Clinical, 18 F‐dopa PET, and genetic analysis of an ethnic Chinese kindred with early‐onset parkinsonism and parkin gene mutations

Lack of Nigral Pathology in Transgenic Mice Expressing Human a-Synuclein Driven by the Tyrosine Hydroxylase Promoter

NEUROGENETICS: A GUIDE FOR CLINICIANS. 2012. Edited by WoodNicholas W.. Published by Cambridge University Press. 241 pages. C$70.00 approx

Accurate determination of ataxin-2 polyglutamine expansion in patients with intermediate-range repeats

Strain and temperature dependent aggregation of Candida auris is attenuated by inhibition of surface amyloid proteins

Weekend specialist intensity and admission mortality in acute hospital trusts in England: a cross-sectional study

Dynamic aberrometer/topographer designed for clinical measurement and treatment of highly aberrated eyes

Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions

Management of Obstructive Sleep Apnea: An Evidence-Based, Multidisciplinary Textbook

Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias: e1004606

Leg Ulcers in Sickle Cell Anemia Are Associated with Laboratory Markers of Hemolysis and SNPs in KL and Genes of the TGF-β/BMP Pathway

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