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Федеральное государственное бюджетное учреждение «Научно-исследовательский институт комплексных проблем сердечно-сосудистых заболеваний» Сибирского отделения Российской академии медицинских наук, Кемерово, Россия
S. V. Ivanov,A. N. Sumin,Y. V. Kazachek,D. E. Philipiev,S. M. Gusev,E. S. Malyshenko,L. S. Barbarash +6 more
TLDR
The outcomes of CAD surgical treatment were improved in this group of patients due to the implementation of a mul-assisted revascularization of coronary and non-coronary arteries.Abstract:
Results. The incidence rate of significant non-cardiac occlusive stenotic lesions in patients with coronary artery disease (CAD), who had to undergo CABG, was 15,84 %. Simultaneous revascularization of coronary and non-coronary arteries was performed in 2,46 % of patients with CAD and PolyVD and multi-stage surgical proced ures were chosen in other cases. Conclusions. The outcomes of CAD surgical treatment were improved in this group of patients due to the implementation of a mul-read more
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Adhesion and Adhesives
TL;DR: Adhesion and AdhesivesEdited by Dr. R. Houwink and Dr. G. Salomon.
References
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Multiscale micromechanical modeling of polymer/clay nanocomposites and the effective clay particle
TL;DR: In this article, a multiscale modeling strategy is employed to account for the hierarchical morphology of the nanocomposite: at a lengthscale of thousands of microns, the structure is one of high aspect ratio particles within a matrix; at the lengthscale, the clay particle structure is either (a) exfoliated clay sheets of nanometer level thickness or (b) stacks of parallel clay sheets separated from one another by interlayer galleries of nanometers level height, and the matrix, if semi-crystalline, consists of fine lamella, oriented with respect to
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Common vs. rare allele hypotheses for complex diseases.
TL;DR: The 'Common Disease, Rare Variant (CDRV)' hypothesis argues that multiple rare DNA sequence variations, each with relatively high penetrance, are the major contributors to genetic susceptibility to common diseases.
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HLA DR-DQ Haplotypes and Genotypes and Type 1 Diabetes Risk: Analysis of the Type 1 Diabetes Genetics Consortium Families
Henry A. Erlich,Ana M. Valdes,Janelle A. Noble,Joyce Carlson,Mike Varney,Patrick Concannon,Josyf C. Mychaleckyj,John A. Todd,Persia Bonella,Anna Lisa Fear,Eva Lavant,Anthony Louey,P. V. Moonsamy +12 more
TL;DR: Data indicate that the risk associated with specific HLA haplotypes can be influenced by the genotype context and that the trans-complementing heterodimer encoded by DQA1*0501 and DQB1*0302 confers very high risk.
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Detection of three distinct patterns of T helper cell dysfunction in asymptomatic, human immunodeficiency virus-seropositive patients. Independence of CD4+ cell numbers and clinical staging.
Mario Clerici,N I Stocks,R.A. Zajac,R.N. Boswell,Daniel R. Lucey,Charles S. Via,Gene M. Shearer +6 more
TL;DR: In vitro TH assay used can detect multiple stages of immune dysregulation early in the course of HIV infection and raises the possibility that staging of HIV+ patients should include in vitro TH functional analyses of the type described here.
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Molecular analysis of the association of HLA-B53 and resistance to severe malaria.
Adrian V. S. Hill,John Elvin,Antony C. Willis,M. Aidoo,Catherine E. M. Allsopp,Frances M. Gotch,Xiao-Ming Gao,Masafumi Takiguchi,Brian Greenwood,Alain Townsend +9 more
TL;DR: Findings indicate a possible molecular basis for this HLA-disease association and support the candidacy of liver-stage-specific antigen-1 as a malaria vaccine component.