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TRANSCATHETER AND SURGICAL REPAIR FOR DEGENERATIVE MITRAL REGURGITATION IN THE ELDERLY: MIDTERM RESULTS FROM A PROPENSITY SCORE ANALYSIS
Mike Saji, Marc Katz, Gorav Ailawadi, Dale Fowler, Damien LaPar, Leora Yarboro, Ravi Ghanta, John Kern, John Dent, Michael Ragosta, Scott Lim (2016)
-adjusted Charlson comorbidity index (hazard ratio 1.33, 95% confidence interval 1.16–1.51, p <0.001), New York Heart
GENETIC DETERMINANTS OF ESSENTIAL HYPERTENSION IN THE POPULATION OF TATARS FROM RUSSIA
Timasheva, Y., Nasibullin, T., Imaeva, E., Mirsaeva, G., Mustafina, O. (2016)
and diastolic blood pressure level. We also showed that the rs213045 polymorphism in ECE1 gene was associated
NZ,(N + 4)Z-DIENOIC FATTY ACIDS: A NEW METHOD FOR THE SYNTHESIS AND INHIBITORY ACTION ON TOPOISOMERASE I AND IIA
D’yakonov, Vladimir A., Dzhemileva, Lilya U., Makarov, Aleksey A., Mulyukova, Alfiya R., Baev, Dmitry S, Khusnutdinova, Elza K, Tolstikova, Tatiana G., Dzhemilev, Usein M. (2016)
unsaturated acids containing a 1Z,5Z-diene group in 61–75 % yields and with[98 % selectivity based on the new
NZ,(N + 4)Z-DIENOIC FATTY ACIDS: A NEW METHOD FOR THE SYNTHESIS AND INHIBITORY ACTION ON TOPOISOMERASE I AND IIA
D’yakonov, Vladimir A., Dzhemileva, Lilya U., Makarov, Aleksey A., Mulyukova, Alfiya R., Baev, Dmitry S., Khusnutdinova, Elza K., Tolstikova, Tatiana G., Dzhemilev, Usein M. (2016)
unsaturated acids containing a 1Z,5Z-diene group in 61–75 % yields and with >98 % selectivity based on the new
SPECTRUM AND FREQUENCY OF THE GJB2 GENE PATHOGENIC VARIANTS IN A LARGE COHORT OF PATIENTS WITH HEARING IMPAIRMENT LIVING IN A SUBARCTIC REGION OF RUSSIA (THE SAKHA REPUBLIC)
Barashkov, Nikolay A., Pshennikova, Vera G., Posukh, Olga L., Teryutin, Fedor M., Solovyev, Aisen V., Klarov, Leonid A., Romanov, Georgii P., Gotovtsev, Nyurgun N., Kozhevnikov, Andrey A., Kirillina, Elena V., Sidorova, Oksana G., Vasilyevа, Lena M., Fedotova, Elvira E., Morozov, Igor V., Bondar, Alexander A., Solovyevа, Natalya A., Kononova, Sardana K., Rafailov, Adyum M., Sazonov, Nikolay N., Alekseev, Anatoliy N., Tomsky, Mikhail I., Dzhemileva, Lilya U., Khusnutdinova, Elza K., Fedorova, Sardana A. (2016)
, the spectrum and frequency of the pathogenic variants in exon 1, exon 2 and the flanking intronic regions
IREB2, CHRNA5, CHRNA3, FAM13A & HEDGEHOG INTERACTING PROTEIN GENES POLYMORPHISMS & RISK OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE IN TATAR POPULATION FROM RUSSIA
Korytina, G.F., Akhmadishina, L.Z., Viktorova, E.V., Kochetova, O.V., Viktorova, T.V. (2016)
.64; P-adj=0.0001, OR=1.41 and P-adj=0.0001, OR=1.47]. The C-G haplotype by rs13180 and rs1051730 was a
SIMPLE MORTALITY PROGNOSTIC RISK CALCULATOR FOR PATIENTS WITH ACUTE CORONARY SYNDROME
Zagidullin, N., Travnikova, E., Zagidullin, B., Zulkarneev, R., Zagidullin, S. (2016)
register, 1000 medical records of patients with ACS were analyzed. Patients were divided into the group 1
ISHCEMIC PRECONDITIONING IN CONTRAST-INDUCED NEPHROPATHY PROPHYLACTICS IN PATIENTS WITH MILD CHRONIC KIDNEY FAILUTE
Zagidullin, N., Dunaeva, A., Sherbakova, E., Zagidullin, S. (2016)
-induced nephropathy (KIN) and secondary – the increase of markers. Results: 26 patients were randomized for IP (60.5±1
PREVALENCE AND RISK FACTORS FOR ERECTILE DYSFUNCTION AND LOWER URINARY TRACT SYMPTOMS IN RUSSIAN FEDERATION MEN: ANALYSIS FROM A NATIONAL POPULATION-BASED MULTICENTER STUDY
Korneyev, I.A., Alexeeva, T.A., Al-Shukri, S.H., Bernikov, A.N., Erkovich, A.A., Kamalov, A.A., Kogan, M.I., Pavlov, V.N., Zhuravlev, V.N., Pushkar, D.Y. (2016)
.2%) and 77 (7.1%) respondents, respectively. According to IPSS assessment, LUTSs were present in 649 (59
АНАЛИЗ АССОЦИАЦИЙ ПОЛИМОРФНОГО МАРКЕРА RS7903146 ГЕНА TCF7L2 С САХАРНЫМ ДИАБЕТОМ 2 ТИПА В ТАТАРСКОЙ ЭТНИЧЕСКОЙ ГРУППЕ, ПРОЖИВАЮЩЕЙ В БАШКОРТОСТАНЕ
THE ASSOCIATION OF TCF7L2 RS7903146 POLYMORPHISM WITH TYPE 2 DIABETES MELLITUS AMONG TATARS OF BASHKORTOSTAN
Авзалетдинова, Д.Ш., Шарипова, Л.Ф., Кочетова, О.В., Моругова, Т.В., Эрдман, В.В., Сомова, Р.Ш., Мустафина, О.Е., Avzaletdinova, D.S., Sharipova, L.F., Kochetova, O.V., Morugova, T.V., Erdman, V.V., Somova, R.S., Mustafina, O.E. (2016)
в 59,5 лет), чем у пациентов с генотипами СТ и СС (56,1 лет, Р=0,044). Уровень базального С

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