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Year | Number of Results |
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2020 | 1 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
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Page 1
Pediatric Patients with Sitosterolemia: Next-Generation Sequencing and Biochemical Examination in Clinical Practice.
J Pers Med. 2023 Oct 14;13(10):1492. doi: 10.3390/jpm13101492.
J Pers Med. 2023.
PMID: 37888103
Free PMC article.
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.
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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.
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