Aleksander V Polyakov
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Explore the profile of Aleksander V Polyakov including associated specialties, affiliations and a list of published articles.
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5
Citations
42
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Recent Articles
1.
Glotov A, Chernykh V, Solovova O, Polyakov A, Donnikov M, Kovalenko L, et al.
Genes (Basel)
. 2024 Jan;
15(1).
PMID: 38254935
A male factor, commonly associated with poor semen quality, is revealed in about 50% of infertile couples. gene (Cystic Fibrosis Transmembrane Conduction Regulator) variants are one of the common genetic...
2.
Sedova A, Shtaut M, Bragina E, Sorokina T, Shmarina G, Andreeva M, et al.
Asian J Androl
. 2023 Mar;
25(5):591-597.
PMID: 36891936
We examined a cohort of 93 cystic fibrosis (CF) male patients who were pancreatic-sufficient (PS-CF; n=40) or pancreatic-insufficient (PI-CF; n = 53). Complex semen examination was performed, including standard semen...
3.
Gundorova P, Kuznetcova I, Baydakova G, Stepanova A, Itkis Y, Kakaulina V, et al.
PLoS One
. 2021 Apr;
16(4):e0249608.
PMID: 33822819
A timely detection of patients with tetrahydrobiopterin (BH4) -deficient types of hyperphenylalaninemia (HPABH4) is important for assignment of correct therapy, allowing to avoid complications. Often HPABH4 patients receive the same...
4.
Gundorova P, Stepanova A, Kuznetsova I, Kutsev S, Polyakov A
PLoS One
. 2019 Jan;
14(1):e0211048.
PMID: 30668579
Phenylalanine hydroxylase (PAH) deficiency is responsible for most cases of phenylketonuria (PKU). Furthermore, numerous studies on BH4-sensitive PAH deficiency have been conducted. To date, BH4, a cofactor of PAH, has...
5.
Gundorova P, Zinchenko R, Kuznetsova I, Bliznetz E, Stepanova A, Polyakov A
PLoS One
. 2018 Aug;
13(8):e0201489.
PMID: 30067850
Phenylketonuria is an inherited disease caused by mutations in the phenylalanine hydroxylase gene PAH. Different PAH pathogenic variants occur in different ethnic groups with various frequencies and the incidence of...