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Risk-management decision-making data from a community-based sample of racially diverse women at high risk of breast cancer: rationale, methods, and sample characteristics of the Daughter Sister Mother Project survey.
Padamsee TJ, Bijou C, Swinehart-Hord P, Hils M, Muraveva A, Meadows RJ, Shane-Carson K, Yee LD, Wills CE, Paskett ED. Padamsee TJ, et al. Among authors: muraveva a. Breast Cancer Res. 2024 Jan 11;26(1):8. doi: 10.1186/s13058-023-01753-x. Breast Cancer Res. 2024. PMID: 38212792 Free PMC article.
A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities.
Bukaeva A, Myasnikov R, Kulikova O, Meshkov A, Kiseleva A, Petukhova A, Zotova E, Sparber P, Ershova A, Sotnikova E, Kudryavtseva M, Zharikova A, Koretskiy S, Mershina E, Ramensky V, Zaicenoka M, Vyatkin Y, Muraveva A, Abisheva A, Nikityuk T, Sinitsyn V, Divashuk M, Dadali E, Pokrovskaya M, Drapkina O. Bukaeva A, et al. Among authors: muraveva a. Int J Mol Sci. 2024 Jul 10;25(14):7556. doi: 10.3390/ijms25147556. Int J Mol Sci. 2024. PMID: 39062799 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: muraveva av. Genes (Basel). 2022 Sep 28;13(10):1750. doi: 10.3390/genes13101750. Genes (Basel). 2022. PMID: 36292635 Free PMC article.
Neuropsychological evaluation of cognitive disorders in children after COVID-19.
Troitskaya LA, Plotnikova IA, Avakyan GG, Erokhina VA, Badalyan OL, Muraveva AV, Zelentsova VL, Khodko OK, Safarova ST, Shirokova EI, Rusina EA, Sanina NP, Terentev KV, Rachin AP. Troitskaya LA, et al. Among authors: muraveva av. Eur J Transl Myol. 2022 Jul 15;32(3):10685. doi: 10.4081/ejtm.2022.10685. Eur J Transl Myol. 2022. PMID: 35838578 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: muraveva a. Genes (Basel). 2022 Feb 7;13(2):309. doi: 10.3390/genes13020309. Genes (Basel). 2022. PMID: 35205353 Free PMC article.
15 results