Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease (Q42713950)

5 November 2017

Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease (English)

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5 November 2017

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4

C D Marsden

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5 November 2017

V Planté-Bordeneuve

1

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5 November 2017

M B Davis

series ordinal

2

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5 November 2017

D M Maraganore

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3

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5 November 2017

A E Harding

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5

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5 November 2017

language of work or name

English

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publication date

1 August 1994

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Journal of Neurology, Neurosurgery and Psychiatry

5 November 2017

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5 November 2017

57

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5 November 2017

8

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5 November 2017

911-913

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Strategies for multilocus linkage analysis in humans

5 November 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073072

Parkinson's disease in a Scottish city

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073072

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073072

Oxidative polymorphism of debrisoquine in Parkinson's disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073072

A large kindred with autosomal dominant Parkinson's disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073072

The human CYP2D locus associated with a common genetic defect in drug oxidation: a G1934----A base change in intron 3 of a mutant CYP2D6 allele results in an aberrant 3' splice recognition site

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073072

Identification of the primary gene defect at the cytochrome P450 CYP2D locus

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073072

Deletion of the entire cytochrome P450 CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073072

New insights into the cause of Parkinson's disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073072

Debrisoquine hydroxylation in Parkinson's disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073072

Parkinson's disease in twins studied with 18F-dopa and positron emission tomography

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073072

The identification of presymptomatic parkinsonism: clinical and [18F]dopa positron emission tomography studies in an Irish kindred

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073072

HLA-typing in multiple sclerosis sibling pairs

16 August 2018

1 reference

12 December 2020

A parkinsonian kindred

1 reference

12 December 2020

Debrisoquine oxidation in Parkinson's disease

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12 December 2020

A clinical and genetic study of familial Parkinson's disease

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12 December 2020

Mutant debrisoquine hydroxylation genes in Parkinson's disease

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12 December 2020

Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease

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12 December 2020

Parkinson's disease in 65 pairs of twins and in a set of quadruplets

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12 December 2020

Identifiers

DOI

10.1136/JNNP.57.8.911

1 reference

5 November 2017

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5 November 2017

PubMed publication ID

8057112

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