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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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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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Chapter 28 - Instant Emulsions

Food Colloids: Self-Assembly and Material Science, 2007, p.413-422

2007

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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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Doubts about TMEM230 as a gene for parkinsonism

Nature genetics, 2019-03, Vol.51 (3), p.367-368

Farrer, Matt J

2019

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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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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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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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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), p.e698

2022

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Identifying genetic factors in Parkinson disease

JAMA : the journal of the American Medical Association, 2002-02, Vol.287 (6), p.715

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

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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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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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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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LRRK2: a common pathway for parkinsonism, pathogenesis and prevention?

Trends in molecular medicine, 2006-02, Vol.12 (2), p.76-82

2006

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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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Mutant COQ2 in multiple-system atrophy

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

2014

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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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Mutations in LRRK2 increase phosphorylation of peroxiredoxin 3 exacerbating oxidative stress-induced neuronal death

Human mutation, 2011-12, Vol.32 (12), p.1390-1397

2011

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

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

Chapter 28 - Instant Emulsions

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

Doubts about TMEM230 as a gene for parkinsonism

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

A family with a tau P301L mutation presenting with parkinsonism

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

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

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

Identifying genetic factors in Parkinson disease

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

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

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

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

LRRK2: a common pathway for parkinsonism, pathogenesis and prevention?

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

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

Mutant COQ2 in multiple-system atrophy

Mutant COQ2 in Multiple-System Atrophy

Mutations in LRRK2 increase phosphorylation of peroxiredoxin 3 exacerbating oxidative stress-induced neuronal death

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 by WoodNicholas W.. 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

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

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