N P. Alekseeva
Moscow, MOW, Russian Federation
Last Updated: 09/26/2026
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Found 8 publications
Hearing loss due to mutations in the genes responsible for Usher syndrome
Journal: Vestnik otorinolaringologii
Published: March 11, 2022
Early audiological phenotype in patients with mutations in the USH2A gene.
Journal: International journal of pediatric otorhinolaryngology
Published: October 18, 2021
Clinical features of temporal lobe epilepsy with involvement of the insular lobe
Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: July 20, 2021
Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population.
Journal: International journal of pediatric otorhinolaryngology
Published: June 17, 2020
Hearing loss due to mutations or lack of the gene coding protein stereocillin
Journal: Vestnik otorinolaringologii
Published: June 02, 2020
Epidemiology of hearing loss in children of the first year of life
Journal: Vestnik otorinolaringologii
Published: August 17, 2018
A pharmacogenetic analysis of dopaminergic and opioidergic genes in opioid addicts treated with the combination of naltrexone and guanfacine
Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: January 01, 2016
Stabilization of remission in patients with opioid dependence with naltrexone implant: a pharmacogenetic approach
Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: August 20, 2015
Showing 1-8 of 8
Last Updated: 09/26/2026