| Issue | Title | |
| Vol 2, No 1 (2018) | Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23 gene in child from Russia | Abstract PDF (Rus) |
| Kristina S. Kulikova, Eugeny V. Vasiliev, Vasily M. Petrov, Anatoly N. Tiulpakov | ||
| 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 (Rus) |
| Natalia A. Zubkova, Olesya A. Gioeva, Yulia V. Tikhonovich, Vasily M. Petrov, Evgeny V. Vasiliev, Anatoliy N. Tyulpakov, Ivan I. Dedov | ||
| Vol 1, No 1 (2017) | Perspectives of pharmacogenetics approach to personalized tamoxifen therapy | Abstract PDF (Rus) |
| Marina I. Savelyeva, Julia S. Panchenko, Irina A. Urvantseva, Anna K. Ignatova, Irina V. Poddubnaya | ||
| Vol 1, No 1 (2017) | Pharmacodynamic gene polymorphism and adverse drug reactionsthen applying antipsychotic drugs | Abstract PDF (Rus) |
| Mikhail S. Zastrozhin, Dmitry A. Sychev, Elena A. Grishina, Ludmila M. Savchenko, Evgeny A. Bryun | ||
| 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 (Rus) |
| Dmitriy V. Ivashchenko, Kristina A. Ryzhykova, Zhannet A. Sozaeva, Mikhail S. Zastrozhin, Elena A. Grishina, Lyudmila M. Savchenko, Eugeniy A. Bryun, Dmitriy A. Sychev | ||
| Vol 1, No 1 (2017) | Stages of development and implementation of personalized medicine technologies in clinical practice | Abstract PDF (Rus) |
| Dmitriy A. Sychev | ||
| Vol 1, No 1 (2017) | The personalized approach to neonatal diabetes therapy depending on the genetic defect | Abstract PDF (Rus) |
| Yulia V. Tikhonovich, Natalia A. Zubkova, Anatoly N. Tiulpakov | ||
| Vol 1, No 1 (2017) | The prospect of pluripotent stem cells for diabetes mellitus treatment | Abstract PDF (Rus) |
| Alexandra V. Panova, Daria V. Goliudsova, Sergey L. Kiselev | ||
| 1 - 8 of 8 Items | ||
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Keywords
ABCC8
ATP-sensitive potassium channel
Autosomal dominant hypophosphatemic rickets
DEND-syndrome
FGF23
GCK
HNF4A, personalized therapy
KCNJ11
MODY
NGS
case report
fibroblast growth factor 23
glibenclamide
hyperphosphaturia
hypophosphatemia
iDEND-syndrome
lower extremity deformities
mutation
neonatal diabetes mellitus
pharmacogenetics
pharmacogenomics
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