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Clinical and Genetic Characteristics of Pediatric Patients with Hypophosphatasia in the Russian Population.
Glotov OS, Savostyanov KV, Nagornova TS, Chernov AN, Fedyakov MA, Raspopova AN, Krasnoukhov KN, Danilov LG, Moiseeva NV, Kalinin RS, Tsai VV, Eismont YA, Voinova VY, Vitebskaya AV, Gurkina EY, Kuzenkova LM, Sosnina IB, Pushkov AA, Zhanin IS, Zakharova EY. Glotov OS, et al. Among authors: pushkov aa. Int J Mol Sci. 2022 Oct 26;23(21):12976. doi: 10.3390/ijms232112976. Int J Mol Sci. 2022. PMID: 36361766 Free PMC article.
Genetic Landscape of Nephropathic Cystinosis in Russian Children.
Savostyanov KV, Pushkov AA, Shchagina OA, Maltseva VV, Suleymanov EA, Zhanin IS, Mazanova NN, Fisenko AP, Mishakova PS, Polyakov AV, Balanovska EV, Zinchenko RA, Tsygin AN. Savostyanov KV, et al. Among authors: pushkov aa. Front Genet. 2022 Apr 28;13:863157. doi: 10.3389/fgene.2022.863157. eCollection 2022. Front Genet. 2022. PMID: 35571017 Free PMC article.
Signatures of Dermal Fibroblasts from RDEB Pediatric Patients.
Beilin AK, Evtushenko NA, Lukyanov DK, Murashkin NN, Ambarchian ET, Pushkov AA, Savostyanov KV, Fisenko AP, Rogovaya OS, Vasiliev AV, Vorotelyak EA, Gurskaya NG. Beilin AK, et al. Among authors: pushkov aa. Int J Mol Sci. 2021 Feb 11;22(4):1792. doi: 10.3390/ijms22041792. Int J Mol Sci. 2021. PMID: 33670258 Free PMC article.
Fabry disease in children: a federal screening programme in Russia.
Namazova-Baranova LS, Baranov AA, Pushkov AA, Savostyanov KV. Namazova-Baranova LS, et al. Among authors: pushkov aa. Eur J Pediatr. 2017 Oct;176(10):1385-1391. doi: 10.1007/s00431-017-2992-y. Epub 2017 Sep 4. Eur J Pediatr. 2017. PMID: 28871487 Free PMC article.
Molecular characteristics of patients with glycosaminoglycan storage disorders in Russia.
Chistiakov DA, Savost'anov KV, Kuzenkova LM, Gevorkyan AK, Pushkov AA, Nikitin AG, Pakhomov AV, Vashakmadze ND, Zhurkova NV, Podkletnova TV, Mayansky NA, Namazova-Baranova LS, Baranov AA. Chistiakov DA, et al. Among authors: pushkov aa. Clin Chim Acta. 2014 Sep 25;436:112-20. doi: 10.1016/j.cca.2014.05.010. Epub 2014 May 26. Clin Chim Acta. 2014. PMID: 24875751
Genetic analysis of 17 children with Hunter syndrome: identification and functional characterization of four novel mutations in the iduronate-2-sulfatase gene.
Chistiakov DA, Kuzenkova LM, Savost'anov KV, Gevorkyan AK, Pushkov AA, Nikitin AG, Vashakmadze ND, Zhurkova NV, Podkletnova TV, Namazova-Baranova LS, Baranov AA. Chistiakov DA, et al. Among authors: pushkov aa. J Genet Genomics. 2014 Apr 20;41(4):197-203. doi: 10.1016/j.jgg.2014.01.007. Epub 2014 Feb 4. J Genet Genomics. 2014. PMID: 24780617
[Polymorphic markers Ala455Val of the THBD gene and Arg353Gln of the F7 gene and association with unfavorable outcomes of coronary atherosclerosis in patients with a history of acute ischemic heart disease].
Pushkov AA, Blagodatskikh KA, Nikitin AG, Agapkina IuV, Brovkin AN, Chudakova DA, Evdokimova MA, Aseĭcheva OIu, Osmolovskaia VS, Minushkina LO, Baklanova TN, Talyzin PA, Donetskaia OP, Tereshchenko SN, Dzhaiani NA, Akatova EA, Glezer MG, Galiavich AS, Zakirova VB, Koziolova NA, Iagoda AV, Boeva OI, Horolets EV, Shlyk SV, Volkova EG, Margarian MP, Guz' IO, Konstantinov VO, Sidorenko BA, Zateĭshchikov DA, Nosikov VV. Pushkov AA, et al. Genetika. 2011 Oct;47(10):1386-92. Genetika. 2011. PMID: 22232927 Russian.
13 results