(Q35927013)

11 August 2017

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title

Genetic testing in Parkinson's disease. (English)

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11 August 2017

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4

John Hardy

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11 August 2017

3

Katrina Gwinn-Hardy

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PubMed ID

15503301

11 August 2017

Aideen M McInerney-Leo

series ordinal

1

object named as

Aideen McInerney-Leo

1 reference

11 August 2017

Donald W Hadley

2

1 reference

PubMed ID

15503301

11 August 2017

language of work or name

English

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publication date

1 January 2005

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11 August 2017

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11 August 2017

20

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1

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11 August 2017

1-10

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Systematic review of incidence studies of Parkinson's disease

11 August 2017

1 reference

Vascular parkinsonism: a distinct, heterogeneous clinical entity

21 January 2018

1 reference

Ecogenetics of Parkinson's disease: 4-hydroxylation of debrisoquine

21 January 2018

1 reference

Is Parkinson's disease the heterozygote form of Wilson's disease: PD = 1/2 WD?

21 January 2018

1 reference

Familial aggregation of Parkinson disease: a comparative study of early-onset and late-onset disease

21 January 2018

1 reference

Parkinson disease in twins: an etiologic study

21 January 2018

1 reference

alpha-Synuclein locus triplication causes Parkinson's disease

21 January 2018

1 reference

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 January 2018

1 reference

Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians

21 January 2018

1 reference

Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene

21 January 2018

1 reference

Mapping of a gene for Parkinson's disease to chromosome 4q21-q23

21 January 2018

1 reference

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

21 January 2018

1 reference

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

21 January 2018

1 reference

Alpha-synuclein in Lewy bodies

21 January 2018

1 reference

Hereditary form of parkinsonism--dementia

21 January 2018

1 reference

Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications

21 January 2018

1 reference

The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia

21 January 2018

1 reference

Alpha synuclein promoter and risk of Parkinson's disease: microsatellite and allelic size variability

21 January 2018

1 reference

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

How much phenotypic variation can be attributed to parkin genotype?

21 January 2018

1 reference

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

21 January 2018

1 reference

Association between early-onset Parkinson's disease and mutations in the parkin gene

21 January 2018

1 reference

Parkin disease: a phenotypic study of a large case series

21 January 2018

1 reference

Parkin mutations are frequent in patients with isolated early-onset parkinsonism.

21 January 2018

1 reference

Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study

21 January 2018

1 reference

Functional association of the parkin gene promoter with idiopathic Parkinson's disease

21 January 2018

1 reference

PINK1 mutations are associated with sporadic early-onset parkinsonism

21 January 2018

1 reference

Phenotypic characterisation of autosomal recessive PARK6-linked parkinsonism in three unrelated Italian families

21 January 2018

1 reference

Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: an 18F-dopa PET study

21 January 2018

1 reference

Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease

21 January 2018

1 reference

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

21 January 2018

1 reference

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

21 January 2018

1 reference

Genetic testing in Huntington's disease

21 January 2018

1 reference

Intentions to use predictive testing by those at risk for Huntington's disease: implications for prevention

21 January 2018

1 reference

Attitudes toward direct predictive testing for the Huntington disease gene. Relevance for other adult-onset disorders. The Canadian Collaborative Group on Predictive Testing for Huntington Disease

21 January 2018

1 reference

Uptake of presymptomatic predictive testing for Huntington's disease

21 January 2018

1 reference

Psychological impact of predicting individuals' risks of illness: a systematic review.

21 January 2018

1 reference

Psychological aspects of genetic counselling: a review of the experience with Huntington's disease

21 January 2018

1 reference

The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service

21 January 2018

1 reference

Predisposition genetic testing for late-onset disorders in adults. A position paper of the National Society of Genetic Counselors.

21 January 2018

1 reference

alpha-synuclein gene haplotypes are associated with Parkinson's disease

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MDS.20316

1 reference

11 August 2017

1 reference

PubMed ID

15503301