Zobrazeno 1 - 10
of 77
pro vyhledávání: '"G A, Tavartkiladze"'
Autor:
S. S. Chibisova, E. Alsharjabi, A. S. Zyuzin, E. R. Tsigankova, P. I. Popadyuk, G. A. Tavartkiladze, I. M. Kirichenko
Publikováno v:
Медицинский совет, Vol 0, Iss 14, Pp 63-69 (2022)
Permanent childhood hearing loss is crucial for speech development and restricts learning abilities. Universal newborn hearing screening programs are well established to detect congenital hearing loss and address the need of hearing-impaired babies.
Externí odkaz:
https://doaj.org/article/a06f876c4add479cb1feebba5f947d94
Autor:
S. S. Chibisova, G. S. Tufatulin, L. S. Namazova-Baranova, I. V. Koroleva, E. R. Tsygankova, T. G. Markova, N. N. Volodin, G. A. Tavartkiladze
Publikováno v:
Педиатрическая фармакология, Vol 18, Iss 2, Pp 134-145 (2021)
Background. Nowadays there is a need to revise the Russian list of risk factors of hearing loss and deafness based on their study according to the evidence-based medicine and the analysis of the audiology service capabilities. Moreover, audiologic sc
Externí odkaz:
https://doaj.org/article/82543b889be949e8bf3173fe881b1fab
Autor:
S. S. Chibisova, E. Alsharjabi, A. S. Zyuzin, T. G. Markova, V. I. Popadyuk, G. A. Tavartkiladze
Publikováno v:
Meditsinskiy sovet = Medical Council. 16:107-112
Introduction. Hearing impairments in schoolchildren affects learning and communication. Reliable data on hearing loss prevalence in this group are necessary for planning the audiological care.Aim. To compare data from a population-based study of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a4ea1e580af4974d29441501560236d
https://doi.org/10.21518/2079-701x-2022-16-18-107-112
https://doi.org/10.21518/2079-701x-2022-16-18-107-112
Autor:
A. A. Stepanova, O. R. Ismagilova, N. M. Galeeva, T. G. Markova, G. A. Tavartkiladze, O. Kvlividze, A. V. Polyakov
Publikováno v:
Russian Journal of Genetics. 58:585-592
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfe3a9171ca3f549545ddfd03530e161
https://doi.org/10.1134/s1022795422050106
https://doi.org/10.1134/s1022795422050106
Autor:
E. E. Savelyeva, G. A. Tavartkiladze
Publikováno v:
Медицинский совет, Vol 0, Iss 6, Pp 56-59 (2016)
According to the World Health Organization (WHO) report in 2015, 360 million people suffer from disabling hearing loss worldwide, of which 328 million are adults and 32 million are children [6]. This is over 5% of the world's population. According to
Externí odkaz:
https://doaj.org/article/d52b7d1483a3417297abd79d7f4fbc96
Autor:
Ekaterina Zhilinskaya, Anna Warzybok, M. V. Goykhburg, Maria Boboshko, Birger Kollmeier, G. A. Tavartkiladze
Publikováno v:
International Journal of Audiology. 59:930-940
To validate the Russian matrix sentence test (RUMatrix) for the assessment of speech recognition in quiet and in noise in clinical praxis. The effect of hearing impairment, age, and masking-noise level on speech recognition was examined.All participa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bb51de8791915f566713df9d023c6ae
https://doi.org/10.1080/14992027.2020.1806368
https://doi.org/10.1080/14992027.2020.1806368
Publikováno v:
Human Physiology. 46:119-126
The correlation between ripple spectrum resolution and speech recognition in prelingual and postlingual cochlear implant users was analysed. The test signal had a band-limited rippled spectrum with a bandwidth of 2 octaves. The central frequency of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b7ae1fe9411efc46984636b6b560d56
https://doi.org/10.1134/s0362119720020115
https://doi.org/10.1134/s0362119720020115
Autor:
G A Tavartkiladze, E A Bliznets, E. A. Grigor’eva, A. V. Polyakov, S. S. Chibisova, E. A. Ivanova, T. G. Markova, Russian Scientific
Publikováno v:
Russian Otorhinolaryngology. 19:44-50
To study the prevalence of mutations in the GJB2 gene in deaf and deaf children in the Astrakhan region and compare them with the frequency of mutations in children with hearing impairment living in other regions of the Russian Federation taking into
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9e0a0aabde21d736f7830a42978a579
https://doi.org/10.18692/1810-4800-2020-5-44-50
https://doi.org/10.18692/1810-4800-2020-5-44-50
Autor:
Russian Scientific, A. V. Polyakov, V. V. Khalfina, G A Tavartkiladze, A. A. Stepanova, T. G. Markova, V. A. Nasyrov
Publikováno v:
Russian Otorhinolaryngology. 19:64-71
The purpose of this work was to identify and study the prevalence of mutations in the GJB2 gene encoding the connexin 26 protein in the Kyrgyz Republic. Hearing loss is currently the most widespread disease. This paper presents a study of 89 patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4eb5a26e1d1a14a2f44fda48a99c3162
https://doi.org/10.18692/1810-4800-2020-6-64-71
https://doi.org/10.18692/1810-4800-2020-6-64-71
Autor:
G A Tavartkiladze, S. S. Chibisova, T. G. Markova, E. A. Bliznetz, N N Alekseeva, A. V. Polyakov, M. R. Lalayants, N.M. Galeeva, O. L. Mironovich
Publikováno v:
International journal of pediatric otorhinolaryngology. 138
Congenital sensorineural hearing loss is related to mutations in numerous genes encoding the structures of the inner ear in majority of the cases. Mutations in GJB2 gene are the most frequently identified causes of congenital nonsyndromal hearing los
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b9bf7876d0881b2bf0733efdf23bb69
https://pubmed.ncbi.nlm.nih.gov/32705992
https://pubmed.ncbi.nlm.nih.gov/32705992