| Стптьи на английском языке | |
| Kolářová H., Tesařová M., Švecová Š., Stránecký V., Přistoupilová A., Zima T., Uhrová J., Volgina S.Ya., Zeman J., Honzík T. Lipoprotein lipase deficiency: clinical, biochemical and molecular characteristics in three patients with novel mutations in the LPL gene // Folia Biol (Praha). – 2014. — 60 (5). – P. 235-243. Scopus | https://xn—-7sbbagcetx2agtgd5cs.xn--p1ai/wp-content/uploads/2023/03/File-1.pdf |
| Mirrahimova M.Kh., Khalmatova B.T., Volgina S., Tashmatova G.A. Bronchial asthma: prevalence and risk factors in children living in the industrial zones of the tashkent region. Central Asian Journal of Medicine: Vol. 2020: Iss. 1, Article 3. P. 28-35. Available at: https://uzjournals.edu.uz/tma/vol2020/iss1/3 | |
| Volgina S.Ya., Sokolov A.A. An Analysis of Medical Care Services for Children With Rare Diseases in the Russian Federation. Review. Front. Pharmacol., 24 November 2021. P. 1-14. Scopus IF – 5,81 (2020) (Q-1) (2-х летний IF-5,331, 3-х летний IF-5,483, 4-х летний IF-5,431; SiteScore 6,2 IF 2020 от Web of Science – 4,225 https://doi.org/10.3389/fphar.2021.754073 Al Kaissi Ali, Hilm M., Volgina S., Kenis V., Ryabykh S., Ochirova P., Jemaa L.D., Bouchoucha S., Shboul M., Kircher S.G., Grill F. Desbuquois Syndrome: Misleading Phenotypic Manifestations. J of Clinical Pediatrics and Mother Health. 1 (1). P.1-8. Doi:10.31579/jcpmh.2021/015 Индексация в WorldCat | https://xn—-7sbbagcetx2agtgd5cs.xn--p1ai/wp-content/uploads/2023/03/File-3.pdfhttps://xn—-7sbbagcetx2agtgd5cs.xn--p1ai/wp-content/uploads/2023/03/File-4.pdf |
| Тезисы на английском языке | |
| Volgina S.Ya., Sadykova D., Mustafin I., Shakirova A., Tylki-Szymanska A. Case report: glycosylphosphatidylinositol biosynthesis defect 11 caused by PIGW mutation //Book of abstracts: SSIEM 2019: Annual Symposium of the Society for the Study of Inborn Error of Metabolism, Rotterdam, The Netherlands, 3-6 September 2019. – P. 269-270. | |
| Volgina S.Ya. Diagnosis of glycosylphosphatidylinositol biosynthesis defect 11 //Book of abstracts: 17th International Conference on Rare Diseases «Don’t miss a rare diseases» – 28.06-30.06.2019, Serock. – 2019. – P. 48-49. Volgina S.Ya. Tuberous Sclerosis Complex Diagnostic Criteria Update. XVI International Conference on Rare Diseases “Understanding rare disease”, Serock 28.06-01.07.2018, Poland, 2018. | |
| Volgina S.Ya. Rett syndrome in children //Book of abstracts: 14th International Conference on Rare Diseases «Rare Diseases – Our task» — 1-3.07.2016, Bialobrzegi. – 2016. — P. 39-40. | |
| Volgina S.Ya. Lipoprotein lipase deficiency in an infant //Book of abstracts: 13th European Conference on Rare Diseases «Rare Diseases – Crossing Borders Together» — 2-6.07.2015, Bialobrzegi. – 2015. — P. 45. | |
| Volgina S. Fabry disease in the chidren: from the onset of clinical symptoms until diagnosis //Book of abstracts: 12th European Conference on Rare Diseases «Living With A Rare Disease» — 4-6.07.2014, Spala. – 2014. — P. 43. | |
| Aminova Z., Volgina S., Yafarova S. Health condition of adolescents with child cerebral paralysis // 4th Europaediatrics, Moscow 3-6 July 2009. — Moscow, 2009.- P. 27. |