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[PRENATAL DIAGNOSIS OF FOETAL TRISOMY 3Q WITH PATERNAL ORIGIN].
Stoyanova V, Nedeva N, Linev A, Ivanov H, Petrova P, Krushkov K, Stratieva V, Vachev T. Stoyanova V, et al. Among authors: linev a. Akush Ginekol (Sofiia). 2015;54(3):43-7. Akush Ginekol (Sofiia). 2015. PMID: 26137780 Bulgarian.
Analysis and evaluation of correlation between DNA polymorphism in the genes MTHFR, PAI-1 and serum creatinine, creatinine clearance and albumin/creatinine ratio in morning urine of patients with type 2 diabetes mellitus and diabetic nephropathy.
Nikolov D, Stoyanova VK, Vladimirova-Kitova L, Linev A, Nikolov G, Kitov S. Nikolov D, et al. Among authors: linev a. Folia Med (Plovdiv). 2022 Dec 31;64(6):896-904. doi: 10.3897/folmed.64.e67912. Folia Med (Plovdiv). 2022. PMID: 36876568
Mutations Associated with Imatinib Mesylate Resistance - Review.
Linev AJ, Ivanov HJ, Zhelyazkov IG, Ivanova H, Goranova-Marinova VS, Stoyanova VK. Linev AJ, et al. Folia Med (Plovdiv). 2018 Dec 1;60(4):617-623. doi: 10.2478/folmed-2018-0030. Folia Med (Plovdiv). 2018. PMID: 31188765 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: linev aj. 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.
14 results