(Q34397680)

1 August 2017

title

Mephenytoin and sparteine oxidation: genetic polymorphisms in Denmark (English)

1 reference

1 August 2017

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Drøhse A

1

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1 August 2017

Bathum L

series ordinal

2

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1 August 2017

Brøsen K

series ordinal

3

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1 August 2017

Gram LF

series ordinal

4

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1 August 2017

language of work or name

English

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publication date

1 May 1989

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British Journal of Clinical Pharmacology

1 August 2017

published in

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1 August 2017

volume

27

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1 August 2017

issue

5

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1 August 2017

page(s)

620-625

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A family and population study of the genetic polymorphism of debrisoquine oxidation in a white British population.

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1379929

Sparteine metabolism in Canadian Caucasians

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1379929

Mephenytoin hydroxylation deficiency: kinetics after repeated doses

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1379929

Sparteine oxidation polymorphism in Denmark

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1379929

Interethnic differences in genetic polymorphism of debrisoquin and mephenytoin hydroxylation between Japanese and Caucasian populations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1379929

Genetic polymorphism of mephenytoin p(4')-hydroxylation: difference between Orientals and Caucasians

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1379929

Family studies of mephenytoin hydroxylation deficiency

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1379929

Genetic polymorphism of human cytochrome P-450 (S)-mephenytoin 4-hydroxylase. Studies with human autoantibodies suggest a functionally altered cytochrome P-450 isozyme as cause of the genetic deficiency

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1379929

Characterization of the common genetic defect in humans deficient in debrisoquine metabolism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1379929

Genetically determined variability in acetylation and oxidation. Therapeutic implications

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1379929

Defective N-oxidation of sparteine in man: A new pharmacogenetic defect

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1379929

Importance of genetic factors in the regulation of diazepam metabolism: relationship to S-mephenytoin, but not debrisoquin, hydroxylation phenotype.

6 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1365-2125.1989.TB03426.X

Mephenytoin and sparteine pharmacogenetics in Canadian Caucasians

21 January 2018

1 reference

12 December 2020

Pharmacogenetics of mephenytoin: a new drug hydroxylation polymorphism in man

1 reference

12 December 2020

Mephenytoin hydroxylation deficiency in Caucasians: frequency of a new oxidative drug metabolism polymorphism

1 reference

12 December 2020

Stereoselective mephobarbital hydroxylation cosegregates with mephenytoin hydroxylation

1 reference

12 December 2020

10.1111/J.1365-2125.1989.TB03426.X

Identifiers

DOI

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1 August 2017

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1 August 2017

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