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Генетические проблемы ДНК-портретирования как части ДНК-фенотипирования: обзор
Genetic problems of DNA portrait as part of DNA phenotyping: A review
Chemeris, Alexey V., Khalikov, Airat A., Garafutdinov, Ravil R., Chemeris, Dmitry A., Sakhabutdinova, Assol R., Khaliullina, Aigul F., Galyautdinov, Rushan R., Sagidullin, Rafael H., Aminev, Farit G., Чемерис, А .В ., Халиков, А .А ., Гарафутдинов, Р .Р ., Чемерис, Д .А ., Сахабутдинова, А .Р ., Халиуллина, А .Ф ., Галяутдинов, Р .Р ., Сагидуллин, Р .Х ., Аминев, Ф .Г . (2024)
ВЛИЯНИЕ СТРУКТУРЫ И ХАРАКТЕРА ТЕЧЕНИЯ ПОЛИОРГАННОЙ ДИСФУНКЦИИ НА ИСХОД ПОЛИТРАВМЫ
INFLUENCE OF STRUCTURE AND CHARACTER OF COURSE OF MULTIPLE ORGAN DYSFUNCTION ON OUTCOME OF POLYTRAUMA
ГАБДУЛХАКОВ, РАИЛЬ МУНИРОВИЧ, РАХИМОВА, РИТА ФЛЮРОВНА, ЛУТФАРАХМАНОВ, ИЛЬДАР ИЛЬДУСОВИЧ, БУЛАТОВ, РУСЛАН ДАМИРОВИЧ, Gabdulkhakov R.M., Rakhimova R.F., Lutfarakhmanov I.I., Bulatov R.D. (2019)
INFLUENCE OF STRUCTURE AND CHARACTER OF COURSE OF MULTIPLE ORGAN DYSFUNCTION ON OUTCOME
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)
out in 52 unre lated families with HSP from Bashkortostan by SSCP and following sequencing. Previously
PREVALENCE AND CO-OCCURRENCE OF ADDICTIVE BEHAVIORS AMONG RUSSIAN AND SPANISH YOUTH: A REPLICATION STUDY
Tsai, J., Huh, J., Idrisov, B., Galimov, A., Espada, J.P., Gonzálvez, M.T., Sussman, S. (2016)
results highlight the need to address multiple addictions in health education programming.
A NOVEL PATHOGENIC VARIANT C.975G>A (P.TRP325*) IN THE POU3F4 GENE IN YAKUT FAMILY (EASTERN SIBERIA, RUSSIA) WITH THE X-LINKED DEAFNESS-2 (DFNX2)
BARASHKOV, N.A., KLAROV, L.A., TERYUTIN, F.M., SOLOVYEV, A.V., PSHENNIKOVA, V.G., ROMANOV, G.P., TOMSKY, M.I., FEDOROVA, S.A., KONNIKOVA, E.E., TOBOKHOV, A.V., MOROZOV, I.V., BONDAR, A.A., POSUKH, O.L., DZHEMILEVA, L.U., KHUSNUTDINOVA, E.K. (2018)
in two deaf half-brothers from one Yakut family (Eastern Siberia, Russia) with identical inner ear
GLOBAL, REGIONAL, AND NATIONAL LEVELS OF MATERNAL MORTALITY, 1990–2015: A SYSTEMATIC ANALYSIS FOR THE GLOBAL BURDEN OF DISEASE STUDY 2015
GBD 2015 Maternal Mortality Collaborators (2018)
dissemination of health data; expand coverage and improve quality of family planning services, including access
MOLECULAR AND BIOCHEMICAL STUDY OF GLUTARIC ACIDURIA TYPE 1 IN 49 RUSSIAN FAMILIES: NINE NOVEL MUTATIONS IN THE GCDH GENE
KURKINA, M.V., MIHAYLOVA, S.V., BAIDAKOVA, G.V., SAIFULLINA, E.V., KOROSTELEV, S.A., PYANKOV, D.V., KANIVETS, I.V., YUNIN, M.A., PECHATNIKOVA, N.L., ZAKHAROVA, E.YU (2020)
genetic characteristics of 51 patients diagnosed with GA1 from 49 unrelated families in Russia. We
Современные представления о роли кишечной микробиоты в развитии туберкулеза легких
Modern Concepts about the Role of Gut Microbiota in Development of Pulmonary Tuberculosis
ЮНУСБАЕВА, М. М., БОРОДИНА, Л. Я., ЗАКИРОВА, А. М., ШАРИПОВ, Р. А., ЮНУСБАЕВ, Б. Б., YUNUSBAEVA, М. М., BORODINA, L. Ya., ZAKIROVA, А. М., SHARIPOV, R. A., YUNUSBAYEV, B. B. (2023)
multiple drug resistance
Population Characteristics of the Spectrum and Frequencies of CFTR Gene Mutations in Patients with Cystic Fibrosis from the Republic of Bashkortostan (Russia)
Ayupova, Guzel, Litvinov, Sergey, Akhmetova, Vita, Minniakhmetov, Ildar, Mokrysheva, Natalia, Khusainova, Rita (2024)
of the sample. Results: A total of 35 distinct causal variants were found in 139 cases from 129 families. Five
Analysis of ATL1 Gene Mutations and Clinical Features of the Disease Course in Patients with Hereditary Spastic Paraplegia
Khidiyatova, I.M., Saifullina, E.V., Karunas, A.S., Akhmetgaleyeva, A.F., Kutlubaeva, R.F., Smakova, L.A., Lobov, S.L., Polyakov, A.V., Shchagina, O.A., Kadnikova, V.A., Ryzhkova, O.P., Magzhanov, R.V. (2022)
was performed in 63 unrelated families with HSP from the Republic of Bashkortostan. Two pathogenic variants were

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