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Original Research

Effects of EPHX1 and CYP3A4 polymorphisms on carbamazepine metabolism in epileptic patients

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Pages 117-120 | Published online: 02 Apr 2014

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Read on this site (3)

Dora Janeth Fonseca, Adrien Morel, Kevin Llinás-Caballero, David Bolívar-Salazar & Paul Laissue. (2021) Whole-Exome Sequencing in Patients Affected by Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Reveals New Variants Potentially Contributing to the Phenotype. Pharmacogenomics and Personalized Medicine 14, pages 287-299.
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Giulia Bivona, Caterina Maria Gambino, Giorgia Iacolino & Marcello Ciaccio. (2019) Vitamin D and the nervous system. Neurological Research 41:9, pages 827-835.
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Chahra Chbili, Neila Fathallah, Aicha Laouani, Manel Nouira, Anis Hassine, Sana Ben Amor, Sofiene Ben Ammou, Chaker Ben Salem & Saad Saguem. (2016) Effects of EPHX1 and CYP3A4*22 genetic polymorphisms on carbamazepine metabolism and drug response among Tunisian epileptic patients. Journal of Neurogenetics 30:1, pages 16-21.
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Articles from other publishers (7)

Valentin Yu. Skryabin, Mikhail S. Zastrozhin, Evgeny A. Bryun & Dmitry A. Sychev. (2022) Peculiarities of carbamazepine pharmacogenetics and the most common adverse drug reactions during its use (literature review). Reviews on Clinical Pharmacology and Drug Therapy 20:3, pages 255-267.
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Concetta Scazzone, Luisa Agnello, Giulia Bivona, Bruna Lo Sasso & Marcello Ciaccio. (2020) Vitamin D and Genetic Susceptibility to Multiple Sclerosis. Biochemical Genetics 59:1, pages 1-30.
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Beatriz Carvalho Henriques, Esther H. Yang, Diego Lapetina, Michael S. Carr, Vasyl Yavorskyy, Joshua Hague & Katherine J. Aitchison. (2020) How Can Drug Metabolism and Transporter Genetics Inform Psychotropic Prescribing?. Frontiers in Genetics 11.
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Concetta Scazzone, Luisa Agnello, Bruna Lo Sasso, Anna Maria Ciaccio, Rosaria V Giglio, Giulia Bivona & Marcello Ciaccio. (2019) Vitamin D and Multiple Sclerosis: An Open-Ended Story. The Open Biochemistry Journal 13:1, pages 88-98.
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Dora Janeth Fonseca, Luz Adriana Caro, Diana Carolina Sierra-Díaz, Carlos Serrano-Reyes, Olga Londoño, Yohjana Carolina Suárez, Heidi Eliana Mateus, David Bolívar-Salazar, Ana Francisca Ramírez, Alejandra de-la-Torre & Paul Laissue. (2019) Mutant GNLY is linked to Stevens–Johnson syndrome and toxic epidermal necrolysis. Human Genetics 138:11-12, pages 1267-1274.
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Li Wang, Mei Bai, Tianbo Jin, Jianwen Zheng, Yuhe Wang, Yongjun He, Dongya Yuan & Xue He. (2019) Effects of CYP3A4 Polymorphisms on Drug Addiction Risk Among the Chinese Han Population. Frontiers in Public Health 7.
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Luisa Agnello, Concetta Scazzone, Bruna Lo Sasso, Paolo Ragonese, Salvatore Milano, Giuseppe Salemi & Marcello Ciaccio. (2018) CYP27A1, CYP24A1, and RXR-α Polymorphisms, Vitamin D, and Multiple Sclerosis: a Pilot Study. Journal of Molecular Neuroscience 66:1, pages 77-84.
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