Strokova T - Search Results

1

A kinetic assay of total lipase activity for detecting lysosomal acid lipase deficiency (LAL-D) and the molecular characterization of 18 LAL-D patients from Russia.

Mayanskiy N, Brzhozovskaya E, Pushkov A, Strokova T, Vlasov N, Surkov A, Gundobina O, Savostianov K. Mayanskiy N, et al. Among authors: strokova t. JIMD Rep. 2019 Jun 3;48(1):75-82. doi: 10.1002/jmd2.12050. eCollection 2019 Jul. JIMD Rep. 2019. PMID: 31392116 Free PMC article.

2

The novel synonymous variant in LIPA gene affects splicing and causes lysosomal acid lipase deficiency.

Bychkov IO, Kamenets EA, Filatova AY, Skoblov MY, Mikhaylova SV, Strokova TV, Gundobina OS, Zakharova EY. Bychkov IO, et al. Among authors: strokova tv. Mol Genet Metab. 2019 Jul;127(3):212-215. doi: 10.1016/j.ymgme.2019.06.005. Epub 2019 Jun 15. Mol Genet Metab. 2019. PMID: 31230978

3

Hepatic glycogen synthase (GYS2) deficiency: seven novel patients and seven novel variants.

Kamenets EA, Gusarova EA, Milovanova NV, Itkis YS, Strokova TV, Melikyan MA, Garyaeva IV, Rybkina IG, Nikitina NV, Zakharova EY. Kamenets EA, et al. Among authors: strokova tv. JIMD Rep. 2020 Feb 25;53(1):39-44. doi: 10.1002/jmd2.12082. eCollection 2020 May. JIMD Rep. 2020. PMID: 32395408 Free PMC article.

4

[Functional performance of the cardiovascular system in patients with overweight and obesity].

Bogdanov AR, Derbeneva SA, Strokova TV, Surkov AG, Kaganov BS. Bogdanov AR, et al. Among authors: strokova tv. Vopr Pitan. 2012;81(1):69-74. Vopr Pitan. 2012. PMID: 22642168 Russian.

5

[Age-dependent characteristics of nutritional status and resting metabolism in overweight and obese children].

Pavlovskaia EV, Strokova TV, Surkov AG, Bogdanov AR, Borodina GV, Kutyreva EN, Sentsova TB. Pavlovskaia EV, et al. Among authors: strokova tv. Vopr Pitan. 2014;83(4):42-51. Vopr Pitan. 2014. PMID: 25549473 Russian.

6

[Biomarkers of vitamin status in obese school children].

Beketova NA, Pavlovskaya EV, Kodentsova VM, Vrzhesinskaya OA, Kosheleva OA, Sokolnikov AA, Strokova TV. Beketova NA, et al. Among authors: strokova tv. Vopr Pitan. 2019;88(4):66-74. doi: 10.24411/0042-8833-2019-10043. Epub 2019 Jul 15. Vopr Pitan. 2019. PMID: 31722143 Clinical Trial. Russian.

7

[Nutrition and orphan diseases].

Strokova TV, Bagaeva ME, Zubovich AI, Pavlovskaya EV, Taran NN, Tin IF, Matinyan IA, Dremucheva TA, Kutyreva EA, Vasil'eva EA. Strokova TV, et al. Vopr Pitan. 2020;89(4):193-202. doi: 10.24411/0042-8833-2020-10053. Epub 2020 Jul 29. Vopr Pitan. 2020. PMID: 32986332 Russian.

8

A Clinical Case of a Homozygous Deletion in the APOA5 Gene with Severe Hypertriglyceridemia.

Vasiluev PA, Ivanova ON, Semenova NA, Strokova TV, Taran NN, Chubykina UV, Ezhov MV, Zakharova EY, Dadli EL, Kutsev SI. Vasiluev PA, et al. Among authors: strokova tv. Genes (Basel). 2022 Jun 14;13(6):1062. doi: 10.3390/genes13061062. Genes (Basel). 2022. PMID: 35741823 Free PMC article.

9

[A case report of Byler's syndrome].

Kaganov BS, Strokova TV, Machulan IV, Kamenets EA, Zakharova EIu. Kaganov BS, et al. Among authors: strokova tv. Eksp Klin Gastroenterol. 2012;(1):43-9. Eksp Klin Gastroenterol. 2012. PMID: 22808778 Russian.

10

[The third case report a patient with primary aldosteronism, seizures, and neurologic abnormalities (PASNA) syndrome de novo variant mutations in the CACNA1D gene].

Semenova NA, Ryzhkova OR, Strokova TV, Taran NN. Semenova NA, et al. Among authors: strokova tv. Zh Nevrol Psikhiatr Im S S Korsakova. 2018;118(12):49-52. doi: 10.17116/jnevro201811812149. Zh Nevrol Psikhiatr Im S S Korsakova. 2018. PMID: 30698561 Russian.

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