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  • Book
    James F. Thornton, Jourdan A. Carboy.
    Contents:
    Special considerations for Mohs patients / James Thornton and Jourdan Carboy
    Anesthesia for reconstruction of facial Mohs defects / Jayne Coleman and Javier Marul
    Mohs micrographic surgery / Sean Chen, Divya Srivastava, and Rajiv I. Nijhawan
    Cellular- and tissue-based wound care / James Thornton and Jourdan Carboy
    Full-thickness skin grafts / James Thornton and Jourdan Carboy
    Split-thickness skin grafting / James Thornton and Jourdan Carboy
    Cartilage grafts / James Thornton and Jourdan Carboy
    Pedicled flaps / James Thornton and Jourdan Carboy
    Local flaps / James Thornton and Jourdan Carboy
    Scalp reconstruction / James Thornton and Jourdan Carboy
    Forehead reconstruction / James Thornton and Jourdan Carboy
    Introduction to nose and simple nasal defects / James Thornton and Jourdan Carboy
    Complex nasal defects / James Thornton, Jourdan Carboy, and Nicholas T. Haddock
    Nasal reconstruction based on subunits / James Thornton and Jourdan Carboy
    Eyelid reconstruction / Ronald Mancini
    Cheek reconstruction /
    James Thornton and Jourdan Carboy
    Chin reconstruction / James Thornton and Jourdan Carboy
    Lip reconstruction / James Thornton and Jourdan Carboy
    Ear reconstruction / James Thornton, Jourdan Carboy, and Christopher Derderian
    Intraoperative complications and initial management / James Thornton and Jourdan Carboy
    Management of complications in the acute healing stage / James Thornton and Jourdan Carboy
    Management of complications in the late healing stage / James Thornton and Jourdan Carboy
    Skin graft revisions / James Thornton and Jourdan Carboy
    Local flap revisions / James Thornton and Jourdan Carboy
    Pedicled flap revisions / James Thornton and Jourdan Carboy.
    Digital Access
    Provider
    Version
    Thieme-Connect
    2018
    Thieme MedOne Plastic Surgery
    2018
  • Article
    Botzenhardt U, Klein J, Ziff M.
    J Exp Med. 1978 May 01;147(5):1435-48.
    T-cell cytotoxicity of NZV mice was tested after in vitro sensitization against a group of H-2 identical strains (BALB/c, B10.D2, DBA/2, HW19). A highly significant and unexpected unidirectional cell-mediated lympholysis (CML) reaction by the sensitized NZB effector cells on these targets was found. After sensitization in vitro with stimulator cells of one H-2d strain, NZB effector cells (H-2d) lysed all other H-2d targets and to a lesser degree, some non-H-2d targets (C57BL/10, DBA/1, B10.Q, CBA, B10.S, A.SW). NZB targets were not lysed. Differences in the major histocompatibility region between NZB and other H-2d strains could be excluded as a possible explanation for the observed reaction of NZB (H-2d) against other H-2d strains. These results consequently represent the first description of a primary in vitro CML directed against determinants not coded for in the major histocompatibility complex. The responsible effector cells are demonstrated to be T cells. The CML of NZB against H-2 identiical targets appears best explained by a reaction against minor histocompatibility antigens. This, and the observed cross-reactions, would indicate that the cytotoxic T-cell system in NZB mice is not subjected to restrictions found in all normal mouse strains tested until now under similar conditions. It is suggested that this hyperreactivity is related to the autoimmune responsiveness of the NZB strain.
    Digital Access Access Options