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  • Book
    [edited by] Warren J. Manning, Dudley J. Pennell.
    Summary: Cardiovascular Magnetic Resonance provides you with up-to-date clinical applications of cardiovascular MRI for the broad spectrum of cardiovascular diseases, including ischemic, myopathic, valvular, and congenital heart diseases, as well as great vessel and peripheral vascular disease. Editors Warren J. Manning and Dudley J. Pennell and their team of international contributors cover everything from basic MR physics to sequence design, flow quantification and spectroscopy to structural anatomy and pathology. Learn the appropriate role for CMR in a variety of clinical settings with reference to other modalities, practical limitations, and costs. With the latest information on contrast agents, MR angiography, MR spectroscopy, imaging protocols, and more, this book is essential for both the beginner and expert CMR practitioner. Covers both the technical and clinical aspects of CMR to serve as a comprehensive reference. Demonstrates the full spectrum of the application of cardiac MR from ischemic heart disease to valvular, myopathic, pericardial, aortic, and congenital heart disease. Includes coverage of normal anatomy, orientation, and function to provide you with baseline values. Discusses advanced techniques, such as interventional MR, to include essential information relevant to the specialist. Features appendices with acronyms and CMR terminology used by equipment vendors that serve as an introduction to the field. Uses consistent terminology and abbreviations throughout the text for clarity and easy reference.

    Contents:
    Section 1. Basic principles of cardiovascular magnetic resonance
    section 2. Ischemic heart disease
    section 3. Right ventricular and congenital heart disease
    section 4. Vasculature and pericardium
    section 5. Functional cardiovascular disease.
    Digital Access ScienceDirect 2010
  • Article
    Brouet JC, Chevalier A.
    J Immunol. 1979 Jan;122(1):260-4.
    Several rabbit antisera to T cells obtained from various sources (thymus, peripheral blood, brain, T-derived leukemias) were studied with the aim to obtain reagents specific for a subset of T cells. Sera were first absorbed on human tissues and B cells; thereafter these T cell-specific sera were additionally absorbed with T cells of different origin and especially with leukemic T cells, which are likely to represent a clonal expnasion of a subset of T cells with potentially unique antigenic markers. Three antigenically distinct subpopulations of T cells were delineated. The relationship of these subsets with previously defined human T cell subpopulations (T subsets with a receptor for the Fc or IgG or IgM or with a receptor for a lectin from wheat germ agglutinin) was investigated.
    Digital Access Access Options