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Page 1
Severe Course of COVID-19 and Long-COVID-19 in Children: Difficulties in Diagnosis.
Vasichkina E, Kofeynikova O, Fetisova S, Starshinova AY, Sheyanova E, Vershinina T, Ryzhkov A, Skripnik A, Alekseeva D, Nechaeva E, Glushkova A, Kudlay D, Pervunina T, Starshinova A. Vasichkina E, et al. Life (Basel). 2023 Mar 14;13(3):781. doi: 10.3390/life13030781. Life (Basel). 2023. PMID: 36983936 Free PMC article.
Sodium current abnormalities and deregulation of Wnt/β-catenin signaling in iPSC-derived cardiomyocytes generated from patient with arrhythmogenic cardiomyopathy harboring compound genetic variants in plakophilin 2 gene.
Khudiakov A, Zaytseva A, Perepelina K, Smolina N, Pervunina T, Vasichkina E, Karpushev A, Tomilin A, Malashicheva A, Kostareva A. Khudiakov A, et al. Among authors: vasichkina e. Biochim Biophys Acta Mol Basis Dis. 2020 Nov 1;1866(11):165915. doi: 10.1016/j.bbadis.2020.165915. Epub 2020 Aug 6. Biochim Biophys Acta Mol Basis Dis. 2020. PMID: 32768677 Free article.
Genetic Spectrum of Left Ventricular Non-Compaction in Paediatric Patients.
Vershinina T, Fomicheva Y, Muravyev A, Jorholt J, Kozyreva A, Kiselev A, Gordeev M, Vasichkina E, Segrushichev A, Pervunina T, Sjoberg G, Skyttner-Rahmani S, Sejersen T, Kostareva A. Vershinina T, et al. Among authors: vasichkina e. Cardiology. 2020;145(11):746-756. doi: 10.1159/000510439. Epub 2020 Oct 13. Cardiology. 2020. PMID: 33049752
A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report.
Zlotina A, Melnik O, Fomicheva Y, Skitchenko R, Sergushichev A, Shagimardanova E, Gusev O, Gazizova G, Loevets T, Vershinina T, Kozyrev I, Gordeev M, Vasichkina E, Pervunina T, Kostareva A. Zlotina A, et al. Among authors: vasichkina e. BMC Med Genomics. 2020 Nov 20;13(1):175. doi: 10.1186/s12920-020-00821-x. BMC Med Genomics. 2020. PMID: 33218365 Free PMC article.
Case Reports: Emery-Dreifuss Muscular Dystrophy Presenting as a Heart Rhythm Disorders in Children.
Kovalchuk T, Yakovleva E, Fetisova S, Vershinina T, Lebedeva V, Lyubimtseva T, Lebedev D, Mitrofanova L, Ryzhkov A, Sokolnikova P, Fomicheva Y, Kozyreva A, Zhuk S, Smolina N, Zlotina A, Pervunina T, Kostareva A, Vasichkina E. Kovalchuk T, et al. Among authors: vasichkina e. Front Cardiovasc Med. 2021 May 7;8:668231. doi: 10.3389/fcvm.2021.668231. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 34026875 Free PMC article.
Case Report: COVID-19-Associated ROHHAD-Like Syndrome.
Artamonova IN, Petrova NA, Lyubimova NA, Kolbina NY, Bryzzhin AV, Borodin AV, Levko TA, Mamaeva EA, Pervunina TM, Vasichkina ES, Nikitina IL, Zlotina AM, Efimtsev AY, Kostik MM. Artamonova IN, et al. Among authors: vasichkina es. Front Pediatr. 2022 Mar 31;10:854367. doi: 10.3389/fped.2022.854367. eCollection 2022. Front Pediatr. 2022. PMID: 35433531 Free PMC article.
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood.
Muravyev A, Vershinina T, Tesner P, Sjoberg G, Fomicheva Y, Čajbiková NN, Kozyreva A, Zhuk S, Mamaeva E, Tarnovskaya S, Jornholt J, Sokolnikova P, Pervunina T, Vasichkina E, Sejersen T, Kostareva A. Muravyev A, et al. Among authors: vasichkina e. Orphanet J Rare Dis. 2022 Sep 14;17(1):358. doi: 10.1186/s13023-022-02477-5. Orphanet J Rare Dis. 2022. PMID: 36104822 Free PMC article.
Case Report: A novel PHOX2B p.Ala248_Ala266dup variant causing congenital central hypoventilation syndrome.
Artamonova IN, Zlotina AM, Ismagilova OR, Levko TA, Kolbina NY, Bryzzhin AV, Smorodin AP, Borodin AV, Mamaeva EA, Sukhotskaya AA, Kagantsov IM, Malysheva DA, Vasichkina ES, Pervunina TM, Petrova NA. Artamonova IN, et al. Among authors: vasichkina es. Front Pediatr. 2023 Feb 15;10:1070303. doi: 10.3389/fped.2022.1070303. eCollection 2022. Front Pediatr. 2023. PMID: 36874254 Free PMC article.
21 results