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  • Book
    editor, Ronald L. Dalman, Editor, Chidester Professor of Surgery, ... Show More Division Chief of Vascular Surgery, Stanford University School of Medicine, Stanford, California, editor-in-chief, Michael W. Mulholland, Professor of Surgery and Chair, Department of Surgery, University of Michigan Medical School, Ann Arbpr, Michigan.
    Summary: This book covers the full range of procedures relating to vascular surgery, including cerebrovascular arterial surgery and intervention, thoracic outlet syndrome management, surgery of the thoracoabdominal aorta, and revascularization procedures.

    Contents:
    Section I. Cerebrovascular arterial surgery/intervention
    section II. Management of the thoracic outlet
    section III. Upper extremity reconstruction/revascularization
    section IV. Thoracic aorta distal to the pericardium
    section V. Hybrid, open and endovascular approaches to the suprarenal abdominal aorta
    section VI. Celiac, mesenteric, splenic, hepatic and renal artery disease management
    section VII. The abdominal aorta and iliac arterial system
    section VIII. Infrainguinal arterial disease management/limb salvage strategies
    section IX. Surgical management of venous disease.
    Digital Access Ovid 2015
    Print Access Request
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    Course Reserves: Request at Lane Information Desk
    2016
    RB112.5 .A664 2016
    1
  • Article
    Owen JS, Ramalho V, Costa JC, Gillett MP.
    Comp Biochem Physiol B. 1979;63(2):261-5.
    1. The cholesterol esterifying activity in mouse plasma has been identified as lecithin:cholesterol acyltransferase (LCAT) on the basis of stoichiometric data, predominant transfer of polyunsaturated fatty acids, wide pH optimum and inhibition of esterification by phospholipase A2 and sulphydryl blocking agents. The esterifying activity differed from that present in plasma of man, rat and other species since it was partially inhibited by mercaptoethanol and other thiols. 2. Stoichiometric correlations between unesterified cholesterol, lecithin and lysolecithin were not exact, suggesting possible involvement of other enzymes in the overall esterification process during in vitro incubation of mouse plasma. 3. The initial rate of cholesterol esterification was determined by in vitro incubation of mouse plasma, whose cholesterol had been labelled by prior in vivo injection of 3H-mevalonic acid. The mean rate was 281 +/- 74 nmol/ml/hr (mean +/- S.D., n = 12) and correlated with unesterified cholesterol concentration (r = 0.73, P less than 0.01).
    Digital Access Access Options