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По вашему запросу найдено документов: 14

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CLINICAL CASE OF ADULT ONSET NIEMANN-PICK DISEASE TYPE C

Saifullina, E.V., Magzhanov, R.V., Mardanova, A.K., Proshlyakova, T.Yu., Zakharova, E.Yu., Klyushnikov, S.A., Illarioshkin, S.N. (2016)

–Pick disease type C (NPC), a rare neurovisceral lysosomal storage disease. It highlights the main clinical

ASSOCIATION OF VARIABLE RS1801282 LOCUS OF PPARG2 GENE WITH DIABETIC NEPHROPATHY

Avzaletdinova, D.Sh., Sharipova, L.F., Kochetova, O.V., Morugova, T.V., Erdman, V.V., Mustafina, O.E. (2016)

-activated receptor gamma) with type 2 diabetes mellitus and its complications was analyzed in inhabitants

TCTAP C-187 CHALLENGING ANATOMY CAROTID ARTERY ANGIOPLASTY COMBINED FEMORAL - RADIAL ROUTE (CFRR)

Buzaev, I.V., Plechev, V.V., Nikolaeva, I.E., Zagitov, I.G. (2016)

branches found type III aortic arch with erosive calcified atherosclerotic plaque, ostial stenosis of left

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)

7903146 polymorphism with type 2 diabetes mellitus (T2DM) among Tatars of Bashkortostan. Materials

ГЕНЕТИЧЕСКИЕ ОСОБЕННОСТИ ПОПУЛЯЦИИ, ПРОЖИВАЮЩЕЙ НА ТЕРРИТОРИИ РЕСПУБЛИКИ БАШКОРТОСТАН

GENETIC CHARACTERISTICS OF THE POPULATION LIVING IN THE TERRITORY OF THE REPUBLIC OF BASHKORTOSTAN

Логинова, М.А., Парамонов, И.В., В.Н. Павлов, Сафуанова, Г.Ш., Loginova, M.A., Paramonov, I.V., Pavlov, V.N., Safuanova, G.Sh. (Вестник трансплантологии и искусственных органов, 2016)

Sequence based typing was used to identify human leukocyte antigen (HLA)-A, -B, -C, -DRB1 alleles

ОСОБЕННОСТИ РЕМОДЕЛИРОВАНИЯ ЛЕВОГО ЖЕЛУДОЧКА У БОЛЬНЫХ ОСТРЫМ ИНФАРКТОМ МИОКАРДА С ПОДЪЕМОМ И БЕЗ ПОДЪЕМА СЕГМЕНТА ST

LEFT VENTRICULAR REMODELING IN PATIENTS WITH ACUTE MYOCARDIAL INFARCTION WITH AND WITHOUT ST SEGMENT ELEVATION

Закирова, Н.Э., Казиева, З.А., Закирова, А.Н., Zakirova, N.E., Kazieva, Z.A., Zakirova, A.N. (2016)

35 healthy men. Structural and functional state of the LV myocardium and types of its remodeling were

PYROPTOSIS IS INVOLVED IN THE PATHOGENESIS OF HUMAN HEPATOCELLULAR CARCINOMA

Chu, Q., Jiang, Y., Zhang, W., Xu, C., Du, W., Tuguzbaeva, G., Qin, Y., Li, A., Zhang, L., Sun, G., Cai, Y., Feng, Q., Li, G., Li, Y., Yang, B. (2016)

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)

frequent GJB2 pathogenic variant in the Yakut patients was c.-23+1G>A (51.82%) and that the second most

TCTAP C-025 EMBOLIC MYOCARDIAL INFARCTION CAUSED BY LEFT ATRIUM EMBOLI FROM ATRIAL FIBRILLATION

Zagitov, I.G., Plechev, V.V., Nikolaeva, I.E., Buzaev, I.V. (2016)

TCTAP C-025 EMBOLIC MYOCARDIAL INFARCTION CAUSED BY LEFT ATRIUM EMBOLI FROM ATRIAL FIBRILLATION

TWO NOVEL MUTATIONS IN GENE SPG4 IN PATIENTS WITH AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA

Akhmetgaleyevaa, A.F., Khidiyatovaa, I.M., Saifullinac, E.V., Idrisovad, R.F., Magzhanov, R.V., Khusnutdinovaa, E.K. (2016)

undescribed frameshift mutations c.322del29 (p.Val108SerfsX18) and c.885del10 (p.Thr295ThrfsX16) were detected

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