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ГЕНЕТИЧЕСКИЕ МАРКЕРЫ ОСТЕОАРТРИТА У ЖЕНЩИН С НЕДИФФЕРЕНЦИРОВАННОЙ ДИСПЛАЗИЕЙ СОЕДИНИТЕЛЬНОЙ ТКАНИ
SEARCH FOR OSTEOARTHRITIS GENETIC MARKERS IN WOMEN WITH UNDIFFERENTIATED CONNECTIVE TISSUE DYSPLASIA
Khusainova, R.I., Tyurin, A.V., Shapovalova, D.A., Khusnutdinova, E.K., Хусаинова Р.И., Тюрин А.В., Шаповалова Д.А., Хуснутдинова Э.К. (2017)
women taking into account the localization of the pathological process, the age of disease manifestation
GENETIC ASPECTS OF KERATOCONUS DEVELOPMENT
Bikbova, M.M., Usubova, E.L., Oganisyana, K.Kh., Lobov, S.L., Khasanovad, R.R., Dzhemilevab, L.U., Khusnutdinova, E.K. (2017)
with keratoconus, firstly, show marked genetic heterogeneity of the disease and, secondly, are associated
MATERIALS OF THE SCIENTIFIC-PRACTICAL CONFERENCE WITH INTERNATIONAL PARTICIPATION "MODERN APPROACHES AND PROSPECTS OF GENETIC RESEARCH IN YAKUTIA", SEPTEMBER 7, 2017, YAKUTSK
Akhmadeeva, G.N., Khidiyatova, I.M., Nasibullin, T.R., Baitimerov, A.R., Magzhanov, R.V., Khusnutdinova, F.K. (2017)
The dopamine metabolism disorder played a major role in the pathogenesis of Parkinson's disease (PD
THE ASSOCIATION OF THE PTPN22 RS2476601 GENE POLYMORPHISM WITH JUVENILE IDIOPATHIC ARTHRITIS IN CHILDREN FROM RUSSIA
Nazarova, L.S., Danilko, K.V., Malievsky, V.A., Viktorova, T.V. (2017)
. The exact cause of the disease is still unknown, but seems to be related to both genetic and environmental
COMPREHENSIVE EVALUATION OF DECELLULARIZED PORCINE CORNEAL AFTER CLINICAL TRANSPLANTATION
Shi, Y., Bikkuzin, T., Song, Z., Jin, X., Jin, H., Li, X., Zhang, H. (2017)
Corneal disease is the second most common blinding disease in the world. The shortage of cornea
OPINIONS OF HEARING PARENTS ABOUT THE CAUSES OF HEARING IMPAIRMENT OF THEIR CHILDREN WITH BIALLELIC GJB2 MUTATIONS
Solovyev, A.V., Dzhemileva, L.U., Posukh, O.L., Barashkov, N.A., Bady-Khoo, M.S., Lobov, S.L., Popova, N.Y., Romanov, G.P., Sazonov, N.N., Bondar, A.A., Morozov, I.V., Tomsky, M.I., Fedorova, S.A., Khusnutdinova, E.K. (2017)
sensory disorder. The results of the molecular-based studies of HI are widely used in various genetic test
ПОЛИМОРФНЫЕ ВАРИАНТЫ ГЕНОВ ГЛУТАМАТНЫХ (GRIK5, GRIN2B) И СЕРОТОНИНОВОГО (HTR2A) РЕЦЕПТОРОВ АССОЦИИРОВАНЫ С ХРОНИЧЕСКОЙ ОБСТРУКТИВНОЙ БОЛЕЗНЬЮ ЛЕГКИХ
POLYMORPHIC VARIANTS OF GLUTAMATE RECEPTOR (GRIK5, GRIN2B) AND SEROTONIN RECEPTOR (HTR2A) GENES ARE ASSOCIATED WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE
Korytina, G.F., Akhmadishina, L.Z., Kochetova, O.V., Aznabaeva, Y.G., Zagidullin, Sh.Z., Victorova, T.V., Корытина Г.Ф., Ахмадишина Л.З., Кочетова О.В., Азнабаева Ю.Г., Загидуллин Ш.З., Викторова Т.В. (2017)
Chronic obstructive pulmonary disease (COPD) is a complex chronic inflammatory disease
РАСПРОСТРАНЕННОСТЬ МАРКЕРОВ ХРОНИЧЕСКОЙ БОЛЕЗНИ ПОЧЕК У ПАЦИЕНТОВ С АРТЕРИАЛЬНОЙ ГИПЕРТОНИЕЙ: РЕЗУЛЬТАТЫ ЭПИДЕМИОЛОГИЧЕСКОГО ИССЛЕДОВАНИЯ ХРОНОГРАФ
PREVALENCE OF MARKERS OF CHRONIC KIDNEY DISEASE IN PATIENTS WITH ARTERIAL HYPERTENSION: RESULTS OF EPIDEMIOLOGICAL STUDY CHRONOGRAF
КОБАЛАВА, Ж.Д., ВИЛЛЕВАЛЬДЕ, С.В., БОРОВКОВА, Н.Ю., ШУТОВ, А.М., НИЧИК, Т.Е., САФУАНОВА, Г.Ш., Kobalava Zhanna D., Villevalde S.V., Borovkova N. Yu., Shutov A.M., Nichik T.E., Safuanova G. Sh. (2017)
PREVALENCE OF MARKERS OF CHRONIC KIDNEY DISEASE IN PATIENTS WITH ARTERIAL HYPERTENSION: RESULTS
КОЛИЧЕСТВЕННЫЙ АНАЛИЗ МИКРОБИОТЫ ПАРОДОНТАЛЬНЫХ КАРМАНОВ И СЛЮНЫ МЕТОДОМ ПЦР В РЕЖИМЕ РЕАЛЬНОГО ВРЕМЕНИ ДО И ПОСЛЕ ЛЕЧЕНИЯ ПАРОДОНТИТА
QUANTITATIVE ANALYSIS OF THE MICROBIOTA OF PERIODONTAL POCKETS AND SALIVA BY REAL-TIME PCR BEFORE AND AFTER TREATMENT OF PERIODONTITIS
BAYMIEV, AL. KH., SHVECA, K. YU., MAVZYUTOV, A.R., TAMAROVA, JE. R., BULGAKOVA, A.I., Баймиев А.Х., Швец К.Ю., Мавзютов А.Р., Тамарова Э.Р., Булгакова А.И. (2017)
INVESTIGATION OF THE ROLE OF CYTOKINE GENES POLYMORPHISMS IN THE DEVELOPMENT OF THE URTICARIA IN THE REPUBLIC OF BASHKORTOSTAN
Gimalova, G.K., Karunas, A.S., Khusuntdinova, E.K., Khantimerova, E.F., Zagidullin, S.Z. (2017)
At present, there is a steady increase in the incidence and prevalence of allergic skin diseases

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