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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 3 |
2022 | 3 |
2023 | 1 |
2024 | 0 |
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7 results
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Page 1
Genetic landscape in Russian patients with familial left ventricular noncompaction.
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.
Diversities in the Gut Microbial Patterns in Patients with Atherosclerotic Cardiovascular Diseases and Certain Heart Failure Phenotypes.
Drapkina OM, Ashniev GA, Zlobovskaya OA, Yafarova AA, Dementeva EV, Kaburova AN, Meshkov IO, Sheptulina AF, Kiselev AR, Kontsevaya AV, Zhamalov LM, Koretskiy SN, Pokrovskaya MS, Akinshina AI, Zagaynova AV, Lukashina MV, Kirillov AV, Abramov IA, Tolkacheva LR, Bikaeva IO, Glazunova EV, Shipulin GA, Bobrova MM, Makarov VV, Keskinov AA, Yudin VS, Yudin SM.
Drapkina OM, et al. Among authors: koretskiy sn.
Biomedicines. 2022 Oct 31;10(11):2762. doi: 10.3390/biomedicines10112762.
Biomedicines. 2022.
PMID: 36359282
Free PMC article.
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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: koretskiy sn.
Genes (Basel). 2022 Sep 28;13(10):1750. doi: 10.3390/genes13101750.
Genes (Basel). 2022.
PMID: 36292635
Free PMC article.
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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: koretskiy s.
Genes (Basel). 2022 Feb 7;13(2):309. doi: 10.3390/genes13020309.
Genes (Basel). 2022.
PMID: 35205353
Free PMC article.
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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: koretskiy s.
Int J Mol Sci. 2021 Jun 24;22(13):6775. doi: 10.3390/ijms22136775.
Int J Mol Sci. 2021.
PMID: 34202524
Free PMC article.
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Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset.
Brodehl A, Meshkov A, Myasnikov R, Kiseleva A, Kulikova O, Klauke B, Sotnikova E, Stanasiuk C, Divashuk M, Pohl GM, Kudryavtseva M, Klingel K, Gerull B, Zharikova A, Gummert J, Koretskiy S, Schubert S, Mershina E, Gärtner A, Pilus P, Laser KT, Sinitsyn V, Boytsov S, Drapkina O, Milting H.
Brodehl A, et al. Among authors: koretskiy s.
Int J Mol Sci. 2021 Apr 6;22(7):3786. doi: 10.3390/ijms22073786.
Int J Mol Sci. 2021.
PMID: 33917638
Free PMC article.
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The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy.
Kulikova O, Brodehl A, Kiseleva A, Myasnikov R, Meshkov A, Stanasiuk C, Gärtner A, Divashuk M, Sotnikova E, Koretskiy S, Kharlap M, Kozlova V, Mershina E, Pilus P, Sinitsyn V, Milting H, Boytsov S, Drapkina O.
Kulikova O, et al. Among authors: koretskiy s.
Genes (Basel). 2021 Jan 19;12(1):121. doi: 10.3390/genes12010121.
Genes (Basel). 2021.
PMID: 33478057
Free PMC article.
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