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Platelet functional abnormalities and clinical presentation in pediatric patients with germline RUNX1, ANKRD26, and ETV6 mutations.
Ovsyannikova GS, Fedorova DV, Tesakov IP, Martyanov AA, Ignatova AA, Ponomarenko EA, Zharkov PA, Pavlova AV, Raykina EV, Maschan MA, Panteleev MA, Novichkova GA, Sveshnikova AN, Smetanina NS. Ovsyannikova GS, et al. Among authors: smetanina ns. Haematologica. 2022 Oct 1;107(10):2511-2516. doi: 10.3324/haematol.2022.281340. Haematologica. 2022. PMID: 35796010 Free PMC article. No abstract available.
Free-breathing T2* mapping for MR myocardial iron assessment at 3 T.
Nazarova EE, Tereshchenko GV, Kupriyanov DA, Smetanina NS, Novichkova GA. Nazarova EE, et al. Among authors: smetanina ns. Eur Radiol Exp. 2020 Apr 17;4(1):25. doi: 10.1186/s41747-020-00156-3. Eur Radiol Exp. 2020. PMID: 32303909 Free PMC article.
The hemostasis system in children with hereditary spherocytosis.
Seregina EA, Poletaev AV, Bondar EV, Vuimo TA, Ataullakhanov FI, Smetanina NS. Seregina EA, et al. Among authors: smetanina ns. Thromb Res. 2019 Apr;176:11-17. doi: 10.1016/j.thromres.2019.02.004. Epub 2019 Feb 5. Thromb Res. 2019. PMID: 30763822
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