Single nucleotide variants rs6582147, rs10010305, rs2136810, rs17797829 as new molecular genetic markers of sudden cardiac death

by A. A. Ivanova, V. N. Maksimov, D. I. Moiseeva, S. K. Malyutina, V. P. Novoselov, M. I. Voevoda
Published 2018-11-01

PREDICTIVE ROLE OF CONNEXIN 40 IN THE PATHOGENESIS OF HEREDITARY SICK SINUS SYNDROME

by S. Yu. Nikulina, A. A. Chernova, V. A. Shulman, T. S. Kukushkina, M. I. Voevoda, V. N. Maksimov
Published 2016-01-01

Polymorphism of the LCT gene regulatory region in Turkicspeaking populations of the Altay-Sayan region (southern Siberia)

by I. V. Pilipenko, M. S. Pristyazhnyuk, V. F. Kobzev, M. I. Voevoda, A. S. Pilipenko
Published 2017-02-01

AN INHERITANCE OF IDIOPATHIC CARDIAC CONDUCTION DISORDERS

by S. S. Tretyakova, S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, V. N. Maksimov, M. I. Voevoda, V. N. Chernov
Published 2014-10-01

Organization experience of diagnostic and medicosocial services for patients with Charcot—Marie—Tooth disease in Krasnoyarsk region

by E. V. Glushchenko, N. A. Shnayder, E. A. Kantimirova, E. A. Kozulina, M. I. Voevoda, V. N. Maksimov, A. A. Allakhverdyan
Published 2015-02-01

MULTIFACTOR PREDICTION OF LONG-TERM OUTCOMES OF ACUTE CORONARY SYNDROME WITH SUSTAINED ST SEGMENT ELEVATION

by N. G. Lozhkina, V. N. Maksimov, Yu. I. Ragino, A. D. Kuimov, M. I. Voevoda
Published 2015-09-01

Associations of genetic markers of the sympathoadrenal system and endothelial dysfunction with coronary heart disease on the example of a small Shoriya population

by E. V. Mikhalina, T. A. Mulerova, V. N. Maksimov, M. I. Voevoda, M. Yu. Ogarkov
Published 2018-11-01

The influence of factors on five-year outcomes after acute coronary syndrome

by N. G. Lozhkina, M. Kh. Khasanova, A. A. Tolmacheva, E. A. Najdena, E. A. Stafeeva, V. A. Kozik, V. B. Barbarich, A. D. Kuimov, V. N. Maksimov, M. I. Voevoda
Published 2018-11-01

Association of single nucleotide polymorphisms rs7164665, rs71461059, rs74765750, rs6762529 with sudden cardiac death

by A. A. Ivanova, V. N. Maksimov, S. K. Malutina, V. P. Novoselov, M. I. Voevoda
Published 2019-11-01

Screening of West Siberian patients with primary congenital glaucoma for CYP1B1 gene mutations

by D. E. Ivanoshchuk, S. V. Mikhailova, O. G. Fenkova, E. V. Shakhtshneider, A. Z. Fursova, I. V. Bychkov, M. I. Voevoda
Published 2020-12-01