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卷 97, 编号 9 (2025): Issues of cardiology
Phenotypic clusters of obesity: gender, clinical, laboratory and genetic characteristics
Podzolkov V., Bragina A., Vasilchenko M., Osadchiy K., Pilipenko M., Antonenko V., Mansimova L., Rodionova Y.
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(Rus)
卷 90, 编号 12 (2018)
The prognostic role of depression as a predictor of chronic somatic diseases manifestation
Neznanov N., Kibitov A., Rukavishnikov G., Mazo G.
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(Rus)
卷 79, 编号 6 (2004)
Moleculargenetic and cellular aspects of heart and vessel remodeling in essential hypertension (review)
Shlyakhto E., Konradi A., Moiseeva О.
卷 89, 编号 7 (2017)
Prognostic value of 1q21 amplification in multiple myeloma
Abramova T., Obukhova T., Mendeleeva L., Pokrovskaya O., Gribanova E., Ryzhko V., Grebenyuk L., Nareyko M., Solovyev M., Votyakova O., Kulikov S., Rusinov M., Savchenko V.
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(Rus)
卷 78, 编号 6 (2003)
The role of genetic studies in development ofnephrology
Ignatova M.
卷 89, 编号 5 (2017)
The influence of STAT4 rs7574865 (G/T) polymorphism on the risk of clinical and immunological phenotypes of systemic sclerosis in a Russian patient population: Results of a pilot study
Krylov M., Ananyeva L., Koneva О., Starovoytova M., Desinova O., Ovsyannikova O., Aleksandrova E., Novikov A., Guseva I., Konovalova N., Varlamov D.
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(Rus)
卷 87, 编号 10 (2015)
Hereditary pheochromocytoma-associated syndromes. Part 2
Yukina M., Troshina E., Beltsevich D.
卷 87, 编号 8 (2015)
Type 2 diabetes mellitus: Clinical aspects of genetics, nutrigenetics, and pharmacogenetics
Ametov A., Kamynina L., Akhmedova Z.
卷 87, 编号 9 (2015)
Hereditary pheochromocytoma-associated syndromes. Part 1
Yukina M., Troshina E., Beltsevich D.
卷 92, 编号 10 (2020)
The pharmacogenetics of hypoglycemia and the glycemic variability at the patients ith type 2 diabetes mellitus
Chernikova N., Kamynina L., Ametov A., Sychev D., Grishina E., Ryzhikova K.
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(Rus)
卷 86, 编号 1 (2014)
The contribution of current investigations to understanding the nature of type 2 diabetes mellitus, and treatment perspectives
Ametov A.
卷 92, 编号 9 (2020)
Hypertrophic cardiomyopathy in elderly: causes, diagnostic and treatment approaches
Chumakova O.
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(Rus)
卷 85, 编号 9 (2013)
Endothelial NO synthase and connexin 37 gene polymorphisms as a risk factor for myocardial infarction in subjects without a history of coronary artery disease
Balatskiĭ A., Andreenko E., Samokhodskaia L., Boĭtsov S., Tkachuk V.
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