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Functional aspects of memory and forgetting
Volobuev A.N., Romanchuk P.I., Romanchuk N.P., Krasnov S.V., Davydkin I.L.
Ankylosing spondylitis: genetic aspects
Mordovsky V., Kapustina E., Chernova A., Nikulina S., Aksyutina N., Potupchik T.
DETERMINANTS OF A RISK FOR CHRONIC KIDNEY DISEASE IN DIABETES MELLITUS
Vikulova O., Zheleznyakova A., Nosikov V., Shestakova M.
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.
CARDIAC RHABDOMYOMAS
Delyagin V.M., Balina E.A.
The foundation for stroke prevention in current clinical practice
Shishkova V., Adasheva T., Kapustina L.
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.
A FAMILY CASE OF FABRY DISEASE
Ivanova R., Sukhomyasova A., Gurlnova E., Vasilyev F., Guryeva P., Gorokhova A., Makslmova N.
A CASE OF HEREDITARY DISEASE IN ONE FAMILY HAVING SEVERAL CHILDREN WITH DIFFERENT BIOLOGICAL FATHERS
Kuznetsova M., Zryachkin N., Tsareva Y., Elizarova T.
Chromosomal anomalies. Role of cytogenetic study at the stage of prenatal diagnostics
Morozova V., Aseeva A., Domracheva E., Gleslnger O., Sllklna T.
OSTEOGENESIS IMPERFECTA
Farkhutdlnova L.
OBSTRUCTIVE SLEEP APNEA/HYPOPNEA SYNDROME AND OBESITY
Alekseeva O., Shnaider N., Demko I., Petrova M., Zobova S.
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.
1 - 13 of 13 Items

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