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THE ROLE OF THE NURSE IN THE PREVENTION OF CARDIOVASCULAR DISEASES
Lobov R.A., Sharapova M.V., Denyakina V.V.
a major role among modern medical and social health problems- cardiovascular diseases. The article
Neurohybrid memristive cmos-integrated systems for biosensors and neuroprosthetics
Mikhaylov A., Pimashkin A., Pigareva Y., Gerasimova S., Gryaznov E., Shchanikov S., Zuev A., Talanov M., Lavrov I., Demin V., Erokhin V., Lobov S., Mukhina I., Kazantsev V., Wu H., Spagnolo B.
, Demin, Erokhin, Lobov, Mukhina, Kazantsev, Wu and Spagnolo. Here we provide a perspective concept
Biomechanics of walking before and after surgical treatment of damaged menisci of the knee joint
Skvortsov D.V., Churkin S.N., Akhpashev A.A., Agzamov D.S., Kanaev A.S., Lobov A.N., Plotnikov V.P., Zhuravleva A.I.
A significant part of the knee joint (KJ) damages comprise the lesions of its menisci. Both
Мобильное приложение для контроля расходов и доходов
Лобов, А. В., Мамонов, К. А., Чернышева Т. Ю., Lobov, A. V., Mamonov, K. A., Chernysheva T. Yu.
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.
Abstract: Hereditary spastic paraplegia (HSP) is a group of neurodegenerative disorders with a
ГИДРОЛИЗ ИНУЛИНА В ПРИСУТСТВИИ ЙОДА
МУЛЛАГИЛЬДИНА, К.И., ИВАНОВ, С.П., КОНКИНА, И.Г., ЛОБОВ, А.Н., ДАУТОВА, Л.А., КОЗЛОВ, В.Н., МАКСЮТОВ, Р.Р., МУРИНОВ, Ю.И., ФАЙЗРАХМАНОВ, И.С., Mullagildina, K.I., Ivanov, S.P., Konkina, I.G., Lobov, A.N., Dautova, L.A., Kozlov, V.N., Maxytov, R.R., Murinov, Yu. I., Fayzrakhmanov, I.S.
йода происходит гидролиз инулина с образованием смеси a- и b- изомеров D-глюкозы и D-фруктозы.
HEARING LOSS OF VOLGA-URAL REGION IN RUSSIA
Khusnutdinova, E.K., Dzhemileva, L.U., Lobov, S.L., Kuznetzov, D.U., Nazirova, A.G., Nurgalina, E.M., Barashkov, N.A., Fedorova, S.A.
, 12SrRNA, tRNASer (UCN), SLC26A4 and SLC26A5 in patients with non-syndromic sensorineural hearing
HEARING LOSS OF VOLGA-URAL REGION IN RUSSIA
Khusnutdinova, E.K., Dzhemileva, L.U., Lobov, S.L., Kuznetzov, D.U., Nazirova, A.G., Nurgalina, E.M., Barashkov, N.A., Fedorova, S.A.
, 12SrRNA, tRNASer (UCN), SLC26A4 and SLC26A5 in patients with non-syndromic sensorineural hearing
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.
Abstract Hereditary hearing impairment (HI) caused by recessive GJB2 mutations is a frequent
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.
Abstract Hereditary hearing impairment (HI) caused by recessive GJB2 mutations is a frequent

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