Hyperhomocysteinemia in Patients on Antiepileptic Drugs - Relation to the Mutation of the MTHFR Gene

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023884%3A_____%2F01%3A00004845" target="_blank" >RIV/00023884:_____/01:00004845 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Hyperhomocysteinemia in Patients on Antiepileptic Drugs - Relation to the Mutation of the MTHFR Gene

Original language description

The causes of hyperhomocysteinemia are multifactorial and include both genetic and acquired components (deficiency of vitamins, drug interference). Treatment with some antiepileptic drugs - phenytoin, carbamazepine, primidone or phenobarbital, (hepatic microsomal enzyme inductors) or their combinations is associated with a risk of increased plasma total homocysteine concentrations and deficiencies in vitamins important for homocysteine remethylation., ,

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

FP - Other medical fields

OECD FORD branch

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Project

<a href="/en/project/NE5489" target="_blank" >NE5489: Differentiation of mild hyperhomocysteinemia, its diagnostic significance and possible use as the selective screening in population of children with risk for ca</a><br>

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year

2001

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Clinical Chemistry and Laboratory Medicine

ISSN

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e-ISSN

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Volume of the periodical

39

Issue of the periodical within the volume

suppl.

Country of publishing house

DE - GERMANY

Number of pages

1

Pages from-to

"S341"

UT code for WoS article

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EID of the result in the Scopus database

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