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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