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Application of pharmacogenetics in oncology.
Miteva-Marcheva NN, Ivanov HY, Dimitrov DK, Stoyanova VK. Miteva-Marcheva NN, et al. Among authors: stoyanova vk. Biomark Res. 2020 Aug 17;8:32. doi: 10.1186/s40364-020-00213-4. eCollection 2020. Biomark Res. 2020. PMID: 32821392 Free PMC article. Review.
Autism Spectrum Disorder - A Complex Genetic Disorder.
Ivanov HY, Stoyanova VK, Popov NT, Vachev TI. Ivanov HY, et al. Among authors: stoyanova vk. Folia Med (Plovdiv). 2015 Jan-Mar;57(1):19-28. doi: 10.1515/folmed-2015-0015. Folia Med (Plovdiv). 2015. PMID: 26431091 Review.
Mutations Associated with Imatinib Mesylate Resistance - Review.
Linev AJ, Ivanov HJ, Zhelyazkov IG, Ivanova H, Goranova-Marinova VS, Stoyanova VK. Linev AJ, et al. Among authors: stoyanova vk. Folia Med (Plovdiv). 2018 Dec 1;60(4):617-623. doi: 10.2478/folmed-2018-0030. Folia Med (Plovdiv). 2018. PMID: 31188765 Review.
Epigenetic aspects in schizophrenia etiology and pathogenesis.
Popov NT, Stoyanova VK, Madzhirova NP, Vachev TI. Popov NT, et al. Among authors: stoyanova vk. Folia Med (Plovdiv). 2012 Apr-Jun;54(2):12-6. doi: 10.2478/v10153-011-0082-x. Folia Med (Plovdiv). 2012. PMID: 23101279 Review.
Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children.
Ivanov IS, Azmanov DN, Ivanova MB, Chamova T, Pacheva IH, Panova MV, Song S, Morar B, Yordanova RV, Galabova FK, Sotkova IG, Linev AJ, Bitchev S, Shearwood AM, Kancheva D, Gabrikova D, Karcagi V, Guergueltcheva V, Geneva IE, Bozhinova V, Stoyanova VK, Kremensky I, Jordanova A, Savov A, Horvath R, Brown MA, Tournev I, Filipovska A, Kalaydjieva L. Ivanov IS, et al. Among authors: stoyanova vk. Mol Genet Metab. 2014 Sep-Oct;113(1-2):76-83. doi: 10.1016/j.ymgme.2014.07.017. Epub 2014 Jul 21. Mol Genet Metab. 2014. PMID: 25087164 Free article.
12 results