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Title
Authors
Vol 28, No 4 (2017)
OBSTRUCTIVE SLEEP APNEA/HYPOPNEA SYNDROME AND OBESITY
Alekseeva O., Shnaider N., Demko I., Petrova M., Zobova S.
PDF
(Rus)
Vol 27, No 2 (2016)
INNOVATIVE TREATMENTS FOR CYSTIC FIBROSIS
Kondratyeva Y.
PDF
(Rus)
Vol 35, No 4 (2024)
Functional aspects of memory and forgetting
Volobuev A.N., Romanchuk P.I., Romanchuk N.P., Krasnov S.V., Davydkin I.L.
PDF
(Rus)
Vol 24, No 12 (2013)
THE DEVELOPMENT OF PRIMARY ISCHEMIC STROKE AND THE SPREAD OF DIFFERENT TYPES OF APOLIPOPROTEIN E GENE POLYMORPHISM IN A MOSCOW POPULATION
Shlshkova V., Remennik A., Shklovsky V., Fukalov Y.
PDF
(Rus)
Vol 29, No 11 (2018)
Carriage of cystic fibrosis mutation through the prism of ART (the current state of the problem)
Krasnopolskaya K., Shuginin I., Sesina N., Voskoboeva E., Beketova A.
PDF
(Rus)
Vol 24, No 10 (2013)
DETERMINANTS OF A RISK FOR CHRONIC KIDNEY DISEASE IN DIABETES MELLITUS
Vikulova O., Zheleznyakova A., Nosikov V., Shestakova M.
PDF
(Rus)
Vol 29, No 7 (2018)
The foundation for stroke prevention in current clinical practice
Shishkova V., Adasheva T., Kapustina L.
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(Rus)
Vol 32, No 9 (2021)
CARDIAC RHABDOMYOMAS
Delyagin V.M., Balina E.A.
PDF
(Rus)
Vol 28, No 6 (2017)
A FAMILY CASE OF FABRY DISEASE
Ivanova R., Sukhomyasova A., Gurlnova E., Vasilyev F., Guryeva P., Gorokhova A., Makslmova N.
PDF
(Rus)
Vol 31, No 9 (2020)
Possibilities of using the rs2070744 polymorphism of the endothelial nitric oxide synthase gene for the identification of severe coronary atherosclerosis in young and middle-aged patients with myocardial infarction
Shishkina E.A., Khlynova O.V., Tuev A.V.
PDF
(Rus)
Vol 28, No 6 (2017)
A CASE OF HEREDITARY DISEASE IN ONE FAMILY HAVING SEVERAL CHILDREN WITH DIFFERENT BIOLOGICAL FATHERS
Kuznetsova M., Zryachkin N., Tsareva Y., Elizarova T.
PDF
(Rus)
Vol 30, No 12 (2019)
Ankylosing spondylitis: genetic aspects
Mordovsky V., Kapustina E., Chernova A., Nikulina S., Aksyutina N., Potupchik T.
PDF
(Rus)
Vol 28, No 8 (2017)
OSTEOGENESIS IMPERFECTA
Farkhutdlnova L.
PDF
(Rus)
Vol 30, No 11 (2019)
Chromosomal anomalies. Role of cytogenetic study at the stage of prenatal diagnostics
Morozova V., Aseeva A., Domracheva E., Gleslnger O., Sllklna T.
PDF
(Rus)
1 - 14 of 14 Items

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