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[Actual nutrition in adults with familial hypercholesterolemia].
Blokhina AV, Ershova AI, Kopylova OV, Limonova AS, Karamnova NS, Shvabskaya OB, Kiseleva AV, Derbeneva SA, Meshkov AN, Drapkina OM. Blokhina AV, et al. Among authors: meshkov an. Vopr Pitan. 2023;92(4):49-58. doi: 10.33029/0042-8833-2023-92-4-49-58. Epub 2023 Jun 30. Vopr Pitan. 2023. PMID: 37801454 Russian.
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. 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.
A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy.
Myasnikov RP, Kulikova OV, Meshkov AN, Bukaeva AA, Kiseleva AV, Ershova AI, Petukhova AV, Divashuk MG, Zotova ED, Sotnikova EA, Abisheva AA, Muraveva AV, Koretskiy SN, Popov SV, Utkina MV, Snigir EA, Mitrofanov SI, Konureeva KD, Mershina EA, Sinitsyn VE, Yudin SM, Drapkina OM. Myasnikov RP, et al. Among authors: meshkov an. Genes (Basel). 2022 Sep 28;13(10):1750. doi: 10.3390/genes13101750. Genes (Basel). 2022. PMID: 36292635 Free PMC article.
Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive Diseases.
Sotnikova EA, Kiseleva AV, Kutsenko VA, Zharikova AA, Ramensky VE, Divashuk MG, Vyatkin YV, Klimushina MV, Ershova AI, Revazyan KZ, Skirko OP, Zaicenoka M, Efimova IA, Pokrovskaya MS, Kopylova OV, Glechan AM, Shalnova SA, Meshkov AN, Drapkina OM. Sotnikova EA, et al. Among authors: meshkov an. J Pers Med. 2022 Jul 12;12(7):1132. doi: 10.3390/jpm12071132. J Pers Med. 2022. PMID: 35887629 Free PMC article.
A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene.
Myasnikov R, Bukaeva A, Kulikova O, Meshkov A, Kiseleva A, Ershova A, Petukhova A, Divashuk M, Zotova E, Sotnikova E, Kharlap M, Zharikova A, Vyatkin Y, Ramensky V, Abisheva A, Muraveva A, Koretskiy S, Kudryavtseva M, Popov S, Utkina M, Mershina E, Sinitsyn V, Kogan E, Blagova O, Drapkina O. Myasnikov R, et al. Among authors: meshkov a. Genes (Basel). 2022 Feb 7;13(2):309. doi: 10.3390/genes13020309. Genes (Basel). 2022. PMID: 35205353 Free PMC article.
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