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Page 1
Edoxaban for Thromboembolism Prevention in Pediatric Patients With Cardiac Disease.
Portman MA, Jacobs JP, Newburger JW, Berger F, Grosso MA, Duggal A, Tao B, Goldenberg NA; ENNOBLE-ATE Trial Investigators. Portman MA, et al. J Am Coll Cardiol. 2022 Dec 13;80(24):2301-2310. doi: 10.1016/j.jacc.2022.09.031. Epub 2022 Oct 31. J Am Coll Cardiol. 2022. PMID: 36328157 Free article. Clinical Trial.
Clinical features of pediatric Danon disease and the importance of early diagnosis.
Gandaeva L, Sonicheva-Paterson N, McKenna WJ, Savostyanov K, Myasnikov R, Pushkov A, Zhanin I, Barskiy V, Zharova O, Silnova I, Kaverina V, Sdvigova N, Fisenko A, Arad M, Basargina E. Gandaeva L, et al. Among authors: basargina e. Int J Cardiol. 2023 Oct 15;389:131189. doi: 10.1016/j.ijcard.2023.131189. Epub 2023 Jul 14. Int J Cardiol. 2023. PMID: 37454822
Genetic landscape in Russian patients with familial left ventricular noncompaction.
Meshkov AN, Myasnikov RP, Kiseleva AV, Kulikova OV, Sotnikova EA, Kudryavtseva MM, Zharikova AA, Koretskiy SN, Mershina EA, Ramensky VE, Zaicenoka M, Vyatkin YV, Kharlap MS, Nikityuk TG, Sinitsyn VE, Divashuk MG, Kutsenko VA, Basargina EN, Barskiy VI, Sdvigova NA, Skirko OP, Efimova IA, Pokrovskaya MS, Drapkina OM. Meshkov AN, et al. Among authors: basargina en. Front Cardiovasc Med. 2023 May 24;10:1205787. doi: 10.3389/fcvm.2023.1205787. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 37342443 Free PMC article.
The Double Mutation DSG2-p.S363X and TBX20-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report.
Myasnikov R, Brodehl A, Meshkov A, Kulikova O, Kiseleva A, Pohl GM, Sotnikova E, Divashuk M, Klimushina M, Zharikova A, Pokrovskaya M, Koretskiy S, Kharlap M, Mershina E, Sinitsyn V, Basargina E, Gandaeva L, Barskiy V, Boytsov S, Milting H, Drapkina O. Myasnikov R, et al. Among authors: basargina e. Int J Mol Sci. 2021 Jun 24;22(13):6775. doi: 10.3390/ijms22136775. Int J Mol Sci. 2021. PMID: 34202524 Free PMC article.
[Familial left ventricular noncompaction: phenotypes and clinical course. Results of the multicenter registry].
Kulikova OV, Myasnikov RP, Mershina EA, Pilus PS, Koretskiy SN, Meshkov AN, Kiseleva AV, Kharlap MS, Sinitsyn VE, Sdvigova NA, Gandaeva LA, Barskiy VI, Derevnina YV, Zharova OP, Basargina EN, Boytsov SA, Drapkina OM. Kulikova OV, et al. Among authors: basargina en. Ter Arkh. 2021 Apr 15;93(4):381-388. doi: 10.26442/00403660.2021.04.200677. Ter Arkh. 2021. PMID: 36286770 Russian.
Gene symbol: TAZ. Disease: Barth syndrome.
Tikhomirov E, Averyanova N, Basargina E, Degtyareva T. Tikhomirov E, et al. Among authors: basargina e. Hum Genet. 2008 Oct;124(3):315-6. Hum Genet. 2008. PMID: 18846664 No abstract available.
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