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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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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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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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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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

α-Synuclein Repeat Polymorphisms and Pesticide Exposure in Parkinsonʼs Disease

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

2009

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Mutant COQ2 in multiple-system atrophy

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

2014

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

[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

Volltextzugriff (PDF)

Parkinson’s Genetics: Molecular Insights for the New Millennium

Neurotoxicology (Park Forest South), 2002-10, Vol.23 (4), p.503-514

2002

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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

Volltextzugriff (PDF)

Parkinson's genetics: An embarrassment of riches

Annals of neurology, 2002-01, Vol.51 (1), p.7-8

2002

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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

Volltextzugriff (PDF)

A family with a tau P301L mutation presenting with parkinsonism

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

2002

Volltextzugriff (PDF)

Identifying genetic factors in Parkinson disease

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

2002

Volltextzugriff (PDF)

Genetics of Parkinson's Disease

Science (American Association for the Advancement of Science), 1997-11, Vol.278 (5341), p.1209-1213

1997

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

2002

Volltextzugriff (PDF)

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Doubts about TMEM230 as a gene for parkinsonism

Mutant COQ2 in Multiple-System Atrophy

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

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

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

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

Parkinson’s Genetics: Molecular Insights for the New Millennium

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

Parkinson's genetics: An embarrassment of riches

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

A family with a tau P301L mutation presenting with parkinsonism

Identifying genetic factors in Parkinson disease

Genetics of Parkinson's Disease

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

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