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НАСЛЕДСТВЕННЫЕ НАРУШЕНИЯ РЕЧИ

HEREDITARY SPEECH DISORDERS

Ершов, Н.М., Никифоров, Д.А., Ershov, N.M., Nikiforov, D.A. (2024)

HEREDITARY SPEECH DISORDERS

Genetic Predisposition to Schizophrenia and Depressive Disorder Comorbidity

Shnayder, N.A., Novitsky, M.A., Neznanov, N.G., Limankin, O.V., Asadullin, A.R., Petrov, A.V., Dmitrenko, D.V., Narodova, E.A., Popenko, N.V., Nasyrova, R.F. (2022)

of the pathophysiology and/or genetic predictors of these mental disorders. The aim of this study was to review

Клинико-генетические взаимосвязи у пациентов с алкогольной зависимостью и инсомническими нарушениями в постабстинентном перио де

Clinical and Genetic Relationships in Patients with Alcohol Dependence and Insomnia in the Post-Withdrawal Period

Ефремов, И.С, Efremov, I.S. (2022)

Clinical and Genetic Relationships in Patients with Alcohol Dependence and Insomnia in the Post

Combined Influences of Genetic Factors and Attention Deficit Hyperactivity Disorder on the Development of Dependence on Synthetic Cannabinoids

Gareeva, A.E., Sharafiev, R.R., Akhmetova, E.A., Nasibullin, T.R., Fakhurtdinova, Z.R., Yuldashev, V.L., Asadullin, A.R. (2020)

cannabinoids taking account of the combined influences of genetic predisposition and attention deficit hypera

Genome-Wide Analysis of the Risk Association for the Development of Paranoid Schizophrenia in Russians: Search for Genetic Markers in the 1q43 Chromosomal Region

Gareeva, A.E. (2024)

Abstract: Schizophrenia is a highly hereditary disorder. Genetic risk is associated with a large

Single-Nucleotide Polymorphisms as Biomarkers of Antipsychotic-Induced Akathisia: Systematic Review

Nasyrova, Regina F, Vaiman, Elena E, Repkina, Vera V, Khasanova, Aiperi K, Asadullin, Azat R, Shipulin, German A, Altynbekov, Kuanysh S, Al-Zamil, Mustafa, Petrova, Marina M, Shnayder, Natalia A (2023)

Antipsychotic-induced akathisia (AIA) is a movement disorder characterized by a subjective feeling

Genetic Biomarkers of Antipsychotic-Induced Prolongation of the QT Interval in Patients with Schizophrenia

Vaiman, E.E., Shnayder, N.A., Zhuravlev, N.M., Petrova, M.M., Asadullin, A.R., Al-Zamil, M., Garganeeva, N.R., Shipulin, G.A., Cumming, G., Nasyrova, R.F. (2022)

(LQTS) as a cardiac adverse drug reaction is a multifactorial symptomatic disorder, the development

ГЕНЕТИЧЕСКИЕ ОСОБЕННОСТИ СИНДРОМА ДЕФИЦИТА ВНИМАНИЯ/ГИПЕРАКТИВНОСТИ. СОВРЕМЕННОЕ СОСТОЯНИЕ ПРОБЛЕМЫ

GENETIC PECULIARITIES OF ATTENTION DEFICIT/HYPERACTIVITY DISORDER (ADHD). UPDATE STATUS OF THE PROBLEM

Р. Р. Шарафиев, R. R. Sharafiev, А. Р. Асадуллин, A. R. Asadullin, В. Л. Юлдашев, V. L. Yuldashev, А. В. Анцыборов, A. V. Antsyborov, Л. В. Лямина, L. V. Lyamina, Э. А. Ахметова, E. A. Akhmetova (Медицинский вестник Башкортостана, №4, 2018)

GENETIC PECULIARITIES OF ATTENTION DEFICIT/HYPERACTIVITY DISORDER (ADHD). UPDATE STATUS

A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia

Romanov, G.P., Pshennikova, V.G., Lashin, S.A., Solovyev, A.V., Teryutin, F.M., Cherdonova, A.M., Borisova, T.V., Sazonov, N.N., Khusnutdinova, E.K., Posukh, O.L., Fedorova, S.A., Barashkov, N.A. (2020)

of the prevalence of congenital HL. Since a significant part of congenital HL is due to genetic causes

Population Characteristics of the Spectrum and Frequencies of CFTR Gene Mutations in Patients with Cystic Fibrosis from the Republic of Bashkortostan (Russia)

Ayupova, Guzel, Litvinov, Sergey, Akhmetova, Vita, Minniakhmetov, Ildar, Mokrysheva, Natalia, Khusainova, Rita (2024)

Background/Objectives: Cystic fibrosis (CF) is one of the most common autosomal-recessive disorders

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