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Profil bibliographique

Г А Таварткиладзе

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

136Publications signalées
1245Citations signalées
0Affiliations récentes

Les domaines associés

Hearing, Cochlea, Tinnitus, GeneticsHearing Loss and RehabilitationNoise Effects and ManagementVestibular and auditory disordersEar Surgery and Otitis Media

Les publications récentes

Accès ouvert 2026 article OpenAlex

Joint Committee on Children’s Hearing: Position Statement on Vaccination Prior and After Cochlear Implantation

Г Ш Туфатулин, A. V. Pashkov, Мarina V. Fedoseenko, Lilia R. Selimzyanova et autres

The article presents the position of experts from the Joint Committee on Infant Hearing on the role of immunoprophylaxis in patients with cochlear implants. It emphasizes that viral and bacterial infections are a significant cause of sensorineural hearing loss, underscoring the importance …

ru, ca (code pays fourni par la source)

0 citations Педиатрическая фармакология
2025 article OpenAlex

Balance disorders in hearing impaired children: prevalence, current possibilities of diagnostics and rehabilitation (scoping review)

Г Ш Туфатулин, M.A. Kozarenko, G.V. Chernyak, V. V. Dvoryanchikov et autres

The review is devoted to the problem of balance disorders combined with hearing loss in pediatric population. The balance function is implemented by three systems: visual, somatosensory and vestibular and plays an important role in the child's development. The critical period for …

ru, us (code pays fourni par la source)

0 citations Russian Bulletin of Otorhinolaryngology
Accès ouvert 2025 article OpenAlex

Position Statement of the Joint Committee on Children’s Hearing on Hearing Loss Associated with Congenital Cytomegalovirus Infection

Г Ш Туфатулин, Sof’ya M. Vikhnina, A. V. Pashkov, Е С Гарбарук et autres

Congenital cytomegalovirus infection (cCMV) can cause a wide range of diseases in newborns, it is most often associated with sensorineural hearing loss (SNHL). cCMV is the leading cause of non-hereditary SNHL (up to 25% of all SNHL cases in). SNHL can be …

ru, ch, ca (code pays fourni par la source)

0 citations Педиатрическая фармакология
Accès ouvert 2025 article OpenAlex

Hearing loss configurations in low- and middle-income countries

John Newall, Rebecca Kim, Piers Dawes, Fadwa Alnafjan et autres

OBJECTIVE: The majority of individuals with hearing loss worldwide reside in low- and middle-income countries (LMICs), but there is limited information regarding the characteristics of hearing loss in these regions. This descriptive study aims to address this knowledge gap by analysing audiogram …

au, Égypte, in, jo, Malawi, my, np, ph, ru, hr, ws, Afrique du Sud, th, tr, ir (code pays fourni par la source)

6 citations International Journal of Audiology
Accès ouvert 2024 article OpenAlex

Development of Measures for d/Deaf and Hard of Hearing Stigma: Introduction to the Special Supplement on Stigma Measurement Tools

Melissa A. Stockton, Howard W. Francis, Jessica West, Rachel D. Stelmach et autres

People who are d/Deaf or hard of hearing (d/DHH) often experience stigma and discrimination in their daily lives. Qualitative research describing their lived experiences has provided useful, in-depth insights into the pervasiveness of stigma. Quantitative measures could facilitate further investigation of the …

us, Ghana, ch, in, au, Nigéria, ru (code pays fourni par la source)

15 citations Ear and Hearing
Accès ouvert 2024 article OpenAlex

Towards Comprehensive Newborn Hearing and Genetic Screening in Russia: Perspectives of Implementation

S S Chibisova, Т. В. Маркова, Evgenia Tsigankova, Г А Таварткиладзе

The universal newborn hearing screening (NHS) program was implemented in Russia in 2008 to replace the high-risk newborn hearing screening. More than 95% coverage and significant improvement in early detection and intervention is achieved. Meanwhile, it was shown that current OAE-based hearing …

ru (code pays fourni par la source)

1 citation Journal of Otorhinolaryngology Hearing and Balance Medicine
Accès ouvert 2024 article OpenAlex

Auditory Phenotype of a Novel Missense Variant in the CEACAM16 Gene in a Large Russian Family With Autosomal Dominant Nonsyndromic Hearing Loss

Т Г Маркова, A. V. Polyakov, S S Chibisova, Olesya Sagaydak et autres

Autosomal dominant hearing loss is represented by a large number of genetically determined forms. Over 50 genes associated with dominant nonsyndromic hearing impairments were described. Pathogenic variants in the CEACAM16 gene lead to the development of DFNA4B hearing loss. Currently, 8 pathogenic …

ru (code pays fourni par la source)

1 citation The Journal of International Advanced Otology
Accès ouvert 2024 article OpenAlex

SWOT analysis of Russian universal newborn hearing screening program

M V Kreisman, Г Ш Туфатулин, S S Chibisova, Evgenia Tsigankova et autres

Introduction. The negative impact of congenital hearing loss on child’s development, education and socialization can be reduced by early identification and intervention as a result of universal newborn hearing screening. The screening program needs continuous improvement by monitoring of outcomes and correction …

ru (code pays fourni par la source)

1 citation Health Care of the Russian Federation
Accès ouvert 2024 article OpenAlex

Objective Measures at Different Stages of Cochlear Implantation: A Data Analysis

Г А Таварткиладзе, V V Bakhshinyan

Objectives: The aim of this literature review was to summarize the results of scientific publications on the use of objective electrophysiological methods at different stages of cochlear implantation. The following aspects were evaluated: usefulness of electrocochleography and auditory evoked brainstem response registration …

ru (code pays fourni par la source)

1 citation Medical Research Archives

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