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По вашему запросу найдено документов: 241

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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)

Abstract Hereditary hearing impairment (HI) caused by recessive GJB2 mutations is a frequent

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. (2017)

in various proportions. The data on the prevalence of hereditary non-syndromic sensorineural hearing loss

РУССКОЯЗЫЧНАЯ ВЕРСИЯ ОПРОСНИКА PEACH (ВАЛИДАЦИЯ И НОРМАТИВНЫЕ ДАННЫЕ)

RUSSIAN VERSION OF PEACH SCALE (VALIDATION AND NORMATIVE DATA)

ТУФАТУЛИН, Г.Ш., ЧИНГ, Т., САВЕЛЬЕВА, Е.Е., САВЕЛЬЕВ, Е.С., TUFATULIN, G.SH., CHING, T., SAVELIEVA, E.E., SAVELIEV, E.S. (2021)

HEARING LOSS IN CHILDREN

A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia

Romanov, G.P., Pshennikova, V.G., Lashin, S.A., Solovyev, A.V., Teryutin, F.M., Cherdonova, A.M., Borisova, T.V., Sazonov, N.N., Khusnutdinova, E.K., Posukh, O.L., Fedorova, S.A., Barashkov, N.A. (2020)

of congenital hearing loss (HL) around the world. Sign language (SL) is known as the main type of communication

Prevalence of depression, anxiety and suicidal ideas and associated factors, in particular sensory impairments, in a population of Bashkortostan in Russia

Bikbov, Mukharram M., Gilmanshin, Timur R., Kazakbaeva, Gyulli M., Iakupova, Ellina M., Panda-Jonas, Songhomitra, Zainullin, Rinat M., Fakhretdinova, Albina A., Fakhretdinova, Albina A., Gilemzianova, Leisan I., Khakimov, Dinar A., Miniazeva, Liana A., Jonas, Jost B. (2023)

, namely vision and hearing impairment, which belonged to the determinants of depression and anxiety

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)

of hearing impairment (HI). More than 300 allelic variants have been identified in the GJB2 gene. Spectrum

ПОИСК МУТАЦИЙ В ГЕНЕ ИНТЕРФЕРОН-ИНДУЦИРОВАННОГО ТРАНСМЕМБРАННОГО БЕЛКА 5 (IFITM5) У БОЛЬНЫХ НЕСОВЕРШЕННЫМ ОСТЕОГЕНЕЗОМ

SEARCH FOR MUTATIONS OF THE INTERFERON-INDUCED TRANSMEMBRANE PROTEIN 5 (IFITM5) GENE IN PATIENTS WITH OSTEOGENESIS IMPERFECTA

Зарипова, А.Р., Нургалиева, Л.Р., Тюрин, А.В., Минниахметов, И.Р., Хусаинова, Р.И., Zaripova, A.R., Nurgalieva, L.R., Tyurin, A.V., Minniakhmetov, I.R., Khusainova, R.I. (2019)

СТАЦИОНАРНЫЕ СЛУХОВЫЕ ВЫЗВАННЫЕ ПОТЕНЦИАЛЫ В КЛИНИЧЕСКОЙ ПРАКТИКЕ

AUDITORY EVOKED POTENTIALS ON AN INPATIENT BASIS IN CLINICAL PRACTICE

САВЕЛЬЕВА, Е.Е., ТУФАТУЛИН, Г.Ш., САВЕЛЬЕВ, Е.С., Savelieva, E.E., Tufatulin, G.Sh., Saveliev, E.S. (2020)

HEARING LOSS

Кохлеарная имплантация – эффективный способ реабилитации детей с глубокой степенью потери слуха

Cochlear implantation is an effective way to rehabilitate children with severe hearing loss

Savelev, Evgenii S., Popadyuk, Valentin I., Saveleva, Elena E., Machalov, Anton S., Kirichenko, Irina M., Савельев, Е. С., Попадюк, В. И., Савельева, Е. Е., Мачалов, А. С., Кириченко, И. М. (2025)

Cochlear implantation is an effective way to rehabilitate children with severe hearing loss

Наследственные спастические параплегии

Hereditary spastic paraplegias

Kutlubaeva, R.F., Kutlubaev, M.A., Magzhanov, R.V., Sayfullina, E.V., Khidiyatova, I.M., Кутлубаева, Р.Ф., Кутлубаев, М.А., Магжанов, Р.В., Сайфуллина, Е.В., Хидиятова, И.М. (2023)

Hereditary spastic paraplegias

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