Zobrazeno 1 - 10
of 46
pro vyhledávání: '"T. G. Markova"'
Publikováno v:
Вестник анестезиологии и реаниматологии, Vol 18, Iss 3, Pp 72-78 (2021)
Post-cardiac arrest syndrome is an extremely complex nosology, characterized by high mortality and the development of severe neurological disorders. Predicting the neurological outcome in this pathology is an urgent problem, since it allows determini
Externí odkaz:
https://doaj.org/article/79e8bf8009f14e069e314ecbe280601a
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:
V.G. Pshennikova, Olga L. Posukh, Gabriel Minarik, Nikolay A. Barashkov, Elza Khusnutdinova, Ludevit Kadasi, Aisen V. Solovyev, Alexander Poliakov, Mait Metspalu, Alena Kushniarevich, M. R. Lalayants, Fedor M. Teryutin, E. A. Bliznetz, Marita S. Bady-Khoo, T. G. Markova, Ene Metspalu, Sardana A. Fedorova
Publikováno v:
Human Genetics. 141:697-707
Mutations in the GJB2 gene are known to be a major cause of autosomal recessive deafness 1A (OMIM 220290). The most common pathogenic variants of the GJB2 gene have a high ethno-geographic specificity in their distribution, being attributed to a foun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ea4cb3f6840f4e54226b24f20725f9a
https://doi.org/10.1007/s00439-021-02405-w
https://doi.org/10.1007/s00439-021-02405-w
Publikováno v:
Вестник анестезиологии и реаниматологии, Vol 18, Iss 3, Pp 72-78 (2021)
Post-cardiac arrest syndrome is an extremely complex nosology, characterized by high mortality and the development of severe neurological disorders. Predicting the neurological outcome in this pathology is an urgent problem, since it allows determini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8242ad3a295f09f93b6753a1ce888c51
https://www.vair-journal.com/jour/article/view/542
https://www.vair-journal.com/jour/article/view/542
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:
O. P. Ryzhkova, O. L. Mironovich, E. A. Bliznetz, N N Alekseeva, T. G. Markova, T. I. Golybeva, A. V. Polyakov
Publikováno v:
Russian Journal of Genetics. 55:630-638
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disease characterized by a combination of hearing impairment with preauricular pits, cervical fistulas or cysts, and various renal abnormalities. Mutations in the EYA1 gene are responsible fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bf26fd3a3f9237fb1dddcd3eede6d9d
https://doi.org/10.1134/s1022795419050119
https://doi.org/10.1134/s1022795419050119
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