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Issue Title Abstract File
Vol 2, No 1 (2018) Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23 gene in child from Russia Abstract   PDF
Kulikova K.S., Vasiliev E.V., Petrov V.M., Tiulpakov A.N.
Vol 1, No 1 (2017) Genotype-based personalized correction of glycemic control in patients with MODY due to mutations in GCK, HNF1A AND HNF4A genes Abstract   PDF
Zubkova N.A., Gioeva O.A., Tikhonovich Y.V., Petrov V.M., Vasiliev E.V., Tyulpakov A.N., Dedov I.I.
Vol 1, No 1 (2017) Perspectives of pharmacogenetics approach to personalized tamoxifen therapy Abstract   PDF
Savelyeva M.I., Panchenko J.S., Urvantseva I.A., Ignatova A.K., Poddubnaya I.V.
Vol 1, No 1 (2017) Pharmacodynamic gene polymorphism and adverse drug reactionsthen applying antipsychotic drugs Abstract   PDF
Zastrozhin M.S., Sychev D.A., Grishina E.A., Savchenko L.M., Bryun E.A.
Vol 1, No 1 (2017) Pharmacogenetic evaluation of adverse events’ risk in patients with alcohol withdrawal syndrome taking bromdihydrochlorphenylbenzodiazepine: The role of CYP2C19 gene polymorphisms Abstract   PDF
Ivashchenko D.V., Ryzhykova K.A., Sozaeva Z.A., Zastrozhin M.S., Grishina E.A., Savchenko L.M., Bryun E.A., Sychev D.A.
Vol 1, No 1 (2017) Stages of development and implementation of personalized medicine technologies in clinical practice Abstract   PDF
Sychev D.A.
Vol 1, No 1 (2017) The personalized approach to neonatal diabetes therapy depending on the genetic defect Abstract   PDF
Tikhonovich Y.V., Zubkova N.A., Tiulpakov A.N.
Vol 1, No 1 (2017) The prospect of pluripotent stem cells for diabetes mellitus treatment Abstract   PDF
Panova A.V., Goliudsova D.V., Kiselev S.L.
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