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  • Book
    [edited by] Allen Jeremias, David L. Brown.
    Summary: The new edition of Cardiac Intensive Care--the only textbook dedicated to cardiac intensive care medicine--chronicles the progress made in the diagnosis, assessment, and treatment of patients with critical cardiac illness. Editors Allen Jeremias, MD, MSc and David L. Brown, MD present the landmark discoveries, greater understanding of syndromes, and technological advancements that have helped make clinical cardiology a progressive and interventional field. You'll get coverage of the plethora of noncoronary diseases in the CICU, as well as a complete compendium of up-to-date pharmacologic agents. The new full-color design and layout and nine new chapters give you the latest theoretical, technical, diagnostic, and therapeutic advances in an accessible and visually appealing format. Moreover, the full text is available online at expertconsult.com. Features the authoritative perspectives of a stellar group of contributors - many of whom are the pioneers in the fields they cover - for the best available guidance. Provides the basic science framework for the clinical material through a section on the scientific foundation of cardiac intensive care to give you the complete picture. Presents a pharmacological introduction to the classes of drugs so you know which are most commonly used in the CICU. Covers which noncoronary diseases frequently result in admittance to the CICU to prepare you for those diagnoses that are not of a cardiac nature.

    Contents:
    Section 1. Introduction
    section 2. Scientific foundation of cardiac intensive care
    section 3. Coronary artery disease
    section 4. Noncoronary diseases : diagnosis and management
    section 5. Pharmacologic agents in the CICU
    section 6. Advanced diagnostic and therapeutic techniques : indications and technical considerations.
    Digital Access ScienceDirect 2010
  • Article
    Sprent J, von Boehmer H.
    J Exp Med. 1979 Feb 01;149(2):387-97.
    Parent leads to F1 chimeras were prepared by reconstituting sublethally irradiated H-2 heterozygous mice with marrow cells from one parental strain. Purified parental strain T cells prepared from unprimed chimeras were exposed to sheep erythrocytes in heavily irradiated mice of each of the two parental strains and recovered from thoracic duct lymph of the recipients at either day 1 or day 5 posttransfer. The lymphoborne cells were then tested for their capacity to collaborate in vivo with B cells of the two parental strains. From this approach it was concluded that parent leads to F1 chimera T cells contain two discrete subgroups of T-helper cells, one specific for self H-2 determinants and the other restricted to H-2 determinants of the opposite parental strain. The restrictions mapped to the K-end of the H-2 complex.
    Digital Access Access Options