Zobrazeno 1 - 10
of 91
pro vyhledávání: '"L I Patrushev"'
Publikováno v:
Гинекология, Vol 18, Iss 2, Pp 56-62 (2016)
Objective. To develop the tactics of complex treatment of patients with infertility caused by chronic inflammatory diseases of the pelvic organs to improve the quality pregravid stage and reduce the risk of reproductive losses. Materials and methods.
Externí odkaz:
https://doaj.org/article/37ccc84b864942e2b9b97026bccca3fb
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 10, Iss 3, Pp 293-298 (2015)
Aim. To study the intensity of the intravascular microcoagulation in patients with atherothrombosis (AT), chronic obstructive pulmonary disease (COPD) and thrombophilia.Material and methods. 115 patients were enrolled into the study: 37 patients with
Externí odkaz:
https://doaj.org/article/effa194d4beb4171a37e23264ff803de
Publikováno v:
Гинекология, Vol 17, Iss 3, Pp 9-12 (2015)
Objective: evaluation of the hemostatic system in patients with endometrioid ovarian cysts before and after treatment of various types of surgical exposures.Materials and methods. 90 patients with with endometrioid ovarian cysts were operated, depend
Externí odkaz:
https://doaj.org/article/90d640e5a25440babd5dc4f021f6d397
Publikováno v:
Acta Biomedica Scientifica, Vol 0, Iss 2, Pp 20-23 (2014)
The research is dedicated to the study of characteristics of health of children, whose relatives of 1st and 2nd lines suffered thrombosis of vessels of different caliber and localizations before the age of 50. We examined 28 children of 13,5 ± 4,9 y
Externí odkaz:
https://doaj.org/article/4b53642b5eda4988800689365c000226
Publikováno v:
Acta Biomedica Scientifica, Vol 0, Iss 4, Pp 115-118 (2013)
The article is devoted to the prevalence of polymorphism of genes responsible for thrombophilia among children. The study included 52 children with thrombosis and 59 children without thrombosis. Detects mutations factor V Leiden, G20210A prothrombin
Externí odkaz:
https://doaj.org/article/974387b4b73245478cf714fb1ac35269
Autor:
T M Reshetniak, E V Ostriakova, N L Patrusheva, L I Patrushev, E N Aleksandrova, N V Seredavkina, A V Volkov, E L Nasonov
Publikováno v:
Терапевтический архив, Vol 85, Iss 1, Pp 76-84 (2013)
AIM: To estimate the prevalence of plasminogen activator inhibitor type 1 (PAI-1) gene polymorphism in patients with antiphospholipid syndrome (APS) and its implication in vascular disorders/MATERIAL AND METHODS: The investigation enrolled 138 patien
Externí odkaz:
https://doaj.org/article/eb151046b63444b0b471bf8e616b4787
Publikováno v:
Научно-практическая ревматология, Vol 49, Iss 6, Pp 57-64 (2011)
Externí odkaz:
https://doaj.org/article/405d004d8cc54cc7b2fe6e38e024f937
Autor:
E. V. Ostryakova, N. L. Patrusheva, A. P. Aleksankin, L. I. Patrushev, N. V. Seredavkina, E. N. Aleksandrova, A. V. Volkov, T. M. Reshetnyak
Publikováno v:
Научно-практическая ревматология, Vol 49, Iss 5, Pp 83-88 (2011)
Antifosfolipidnyi sindrom (AFS) – simptomo- kompleks, proyavlyayushchiisya trombozom sosudov razlichnoi lokalizatsii i kalibra pri obyazatel'nom nalichii v krovi antifosfolipidnykh antitel (aFL) [1]. K serologicheskim markeram AFS, soglasno mezhdun
Externí odkaz:
https://doaj.org/article/7cbbddb087a743e8bb6702a344b2d5a0
Autor:
Lyubov' Valer'evna Kondrat'eva, Natal'ya L'vovna Patrusheva, Lev Ivanovich Patrushev, Elena Nikolaevna Aleksandrova, Tat'yana Feliksovna Kovalenko, Ekaterina Viktorovna Ostryakova, Tat'yana Magomedalievna Reshetnyak, L V Kondratyeva, N L Patrusheva, L I Patrushev, E N Aleksandrova, T F Kovalenko, E V Ostryakova, T M Reshetnyak
Publikováno v:
Терапевтический архив, Vol 82, Iss 5, Pp 33-39 (2010)
Aim. To estimate the frequency of relapses of thrombotic and hemorrhagic complications during moderately intensive therapy for antiphospholipid syndrome (APS) with warfarin with and without aspirin. Subjects and methods. Eighty-two patients diagnosed
Externí odkaz:
https://doaj.org/article/4c61a937e6fe4838af1760e1d9be4434
Autor:
Marat S. Pavlyukov, L. I. Patrushev, Mikhail I. Shakhparonov, Alina M. Gamisoniya, Ksenia Anufrieva, Ksenia V. Morozova, T. F. Kovalenko, Lyudmila A. Ozolinya, Mikhail Yu. Bobrov, Yulia E. Dobrokhotova
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 1, p e0243093 (2021)
PLoS ONE, Vol 16, Iss 1, p e0243093 (2021)
The processed pseudogene PTENP1 is involved in the regulation of the expression of the PTEN and acts as a tumor suppressor in many types of malignances. In our previous study we showed that PTENP1 methylation is present not only in tumor, but also in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bad67b2beed45ff56fcfdc7547247c0
http://europepmc.org/articles/PMC7822536
http://europepmc.org/articles/PMC7822536