The role of CYP2C9 polymorphisms in phenytoin-related cerebellar atrophy

Seizure

Volumn 22, Issue 3, 2013, Pages 194-197

  Twardowschy, Carlos A ^a   Werneck, Lineu C ^a   Scola, Rosana H ^a   Borgio, João G ^a   De Paola, Luciano ^a   Silvado, Carlos ^a  

^a FEDERAL UNIVERSITY OF PARANÁ   (Brazil)

Author keywords

Atrophy; Cerebellar; CYP2C9; Phenytoin

Indexed keywords

CYTOCHROME P450 2C9; PHENYTOIN;

ADULT; ARTICLE; BRAIN SIZE; CEREBELLUM ATROPHY; CLINICAL ARTICLE; CONTROLLED STUDY; EPILEPSY; FEMALE; GENETIC POLYMORPHISM; GENOTYPE; GRAY MATTER; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; WHITE MATTER;

ADOLESCENT; ADULT; AGED; ALLELES; ANTICONVULSANTS; ARYL HYDROCARBON HYDROXYLASES; ATROPHY; CEREBELLAR DISEASES; EPILEPSY; FEMALE; GENE-ENVIRONMENT INTERACTION; GENOTYPE; HUMANS; MALE; MIDDLE AGED; PHENYTOIN; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84875226842     PISSN: 10591311     EISSN: 15322688     Source Type: Journal    
DOI: 10.1016/j.seizure.2012.12.004     Document Type: Article

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