Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Yulia Surikova"'
Autor:
Olga Blagova, Indira Alieva, Eugenia Kogan, Alexander Zaytsev, Vsevolod Sedov, S. Chernyavskiy, Yulia Surikova, Ilya Kotov, Elena V. Zaklyazminskaya
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
Hypertrophic cardiomyopathy (HCM) is the most common inherited disease, with a prevalence of 1:200 worldwide. The cause of HCM usually presents with an autosomal dominant mutation in the genes encoding one of more than 20 sarcomeric proteins, incompl
Externí odkaz:
https://doaj.org/article/ca6f0dd9e93c4460a8e8a844d864a906
Autor:
P.J. Benke, Elena Zaklyazminskaya, L. Mallin, C. Armstrong, C.C. Marboe, Marie T. McDonald, Vladimir Kaimonov, D. Mabin, M.S. Balashova, Natalia Shirokova, H.K. Robinson, Inna S. Povolotskaya, Ganka Douglas, D.R. Deyle, Claire L. S. Turner, Kirsty McWalter, Ekaterina Pomerantseva, M.R. Chrisant, Sian Ellard, Yulia Surikova, Katherine Agre
Publikováno v:
Clinical geneticsREFERENCES. 98(4)
Childhood dilated cardiomyopathy (DCM) is a leading cause of heart failure requiring cardiac transplantation and approximately 5% of cases result in sudden death. Knowledge of the underlying genetic cause can aid prognostication and clinical manageme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98a8c488da8b132f34642c2fa7630e79
https://pubmed.ncbi.nlm.nih.gov/32666529
https://pubmed.ncbi.nlm.nih.gov/32666529
Autor:
Margarita E. Polyak, Mikhail Skoblov, Alexandra Filatova, Yulia Surikova, Elena Zaklyazminskaya
Publikováno v:
Gene. 697
Mutations in the MYH7 gene are the source of an allelic series of diseases, including various cardiomyopathies and skeletal myopathies that usually manifest in adulthood. We observed a 1.5 y.o. male patient with congenital weaknesses of the axial mus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8f130e6c21d138735bc0bc863f5ba01
https://pubmed.ncbi.nlm.nih.gov/30794915
https://pubmed.ncbi.nlm.nih.gov/30794915