Maria R Lalayants (M R Lalayants)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 7

Top Topics

Cerebrospinal Fluid

Duchenne Muscular Dystrophy

Spectrum Disorder

Clinical Evaluation

Top Venues

Vestnik otorinolaringologii

This page only lists publications with an associated author ORCID identifier.

Publications

G Sh Tufatulin, Maria R Lalayants, S A Artyushkin, S M Vikhnina, Ekaterina S Garbaruk, V V Dvorjanchikov, I V Koroleva, M V Kreisman, E K Mefodovskaya, A V Pashkov, I V Savenko, E R Tsygankova, Svetlana Chibisova, George Tavarkiladze
[Clinical protocol: audiological assessment of infants in Russian Federation. Part II]. Vestnik otorinolaringologii 88 (6) (2024)
G Sh Tufatulin, Maria R Lalayants, S A Artyushkin, S M Vikhnina, Ekaterina S Garbaruk, V V Dvorjanchikov, I V Koroleva, M V Kreisman, E K Mefodovskaya, A V Pashkov, I V Savenko, E R Tsygankova, Svetlana Chibisova, George Tavarkiladze
[Clinical protocol: audiological assessment of infants in Russian Federation. Part II]. Vestnik otorinolaringologii 88 (6) (2024)
G Sh Tufatulin, Maria R Lalayants, S A Artyushkin, S M Vikhnina, Ekaterina S Garbaruk, V V Dvorjanchikov, I V Koroleva, M V Kreisman, E K Mefodovskaya, A V Pashkov, I V Savenko, E R Tsygankova, Svetlana Chibisova, George Tavarkiladze
[Clinical protocol: audiological assessment of infants in Russian Federation. Part I]. Vestnik otorinolaringologii 88 (5) (2023)
Maria R Lalayants, T I Chugunova, V V Bakhshinyan, George Tavarkiladze
[Electrically evoked ABR through cochlear implant in children with auditory neuropathy spectrum disorder]. Vestnik otorinolaringologii 87 (2) (2022)
Aisen V Solovyev, Alena Kushniarevich, Elena A Bliznetz, Marita Bady-Khoo, Maria R Lalayants, Tatiana G Markova, Gabriel Minárik, L'udevít Kádasi, Ene Metspalu, Vera G Pshennikova, Fedor M Teryutin, Elza K Khusnutdinova, Alexander Poliakov, Mait Metspalu, Olga L Posukh, Nikolay A Barashkov, Sardana A Fedorova
A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia. Human genetics (2021)
Maria R Lalayants, Olga Mironovich, Elena A Bliznetz, Tatiana G Markova, Alexander V Polyakov, George Tavarkiladze
[OTOF-related auditory neuropathy spectrum disorder]. Vestnik otorinolaringologii 85 (2) (2020)
Tatiana G Markova, N N Alekseeva, Olga Mironovich, Elena A Bliznetz, Maria R Lalayants, Alexander V Polyakov, George Tavarkiladze
[Hearing loss due to mutations or lack of the gene coding protein stereocillin]. Vestnik otorinolaringologii 85 (2) (2020)