Allergy Papers: Study of Initial Response and Reversion Rates of Subjects Treated with the Allergy Technique

References

1. Hallbom, T., Smith, S. The Allergy Technique. Anchor Point. October, 1987

2. Andreas, C., Andreas S. Heart of the Mind. Real People Press, Moab, Utah. pp. 37-45, 1989

3. Dilts, R., Hallbom, T., Smith, S. Beliefs, Pathways to Health and Well-being. Metamorphous Press, Portland, OR. pp. 173-189, 1990

4. Swack J. A., Morimoto C., Schlossman S. F., Rudd C. E. The structure and function of a novel activation antigen (2H1) on T-lymphocytes. In: McMichael AJ, et al. eds. Leukocyte Typng III. 2Oxford: Oxford University Press, p.550-554, 1987

5. Rudd, C. E., Trevillyan, J. M., Dasgupta, J. D., Swack, J. A. Schlossman, S. F. The CD4 and CD8 antigens are associated in detergent lysates with a protein-tyrosine kinase (p58Lstra/Lck) from T cells. In Cellular Basis of Immune Modulation, Vol 9: Modulation of the Immune Cell Response. JG Kaplan, DR Green, RC Bleackley, eds. Alan Liss, New York, p.79, 1989

6. Swack, J. A., Gangemi R. M. R., Rudd C. E., Morimoto C., Schlossman S. F., Romain P. L. Structural characterization of CD6: properties of two distinct epitopes involved in T cell activation. Molecular Immunology 26:1037-1049, 1989

7. Gangemi, R. M. R., Swack, J. A., Gaviria, D. M., Romain, P. L. Anti-T12, an anti-CD6 monoclonal antibody, can activate human T lymphocytes. The Journal of Immunology 143:2439-2447, 1989

8. Edwin, C., Swack, J. A., Williams, K., Bonventre, P. F., Kass, E. H. Synthetic peptide derived from toxic shock syndrome toxin 1 activates human T cell proliferation in the presence of monocytes and induces tumor necrosis factor production. Journal of Infectious Diseases 163:524-529, 1991

9. Swack, J. A., Mier, J. W., Romain, P. L., Hull, S. R., Rudd, C. E. Biosynthesis and post-translational modification of CD6 a T cell signal-transducing molecule. The Journal of Biological Chemistry 266:7137-7143, 1991

10. James, T., Woodsmall, W. Time Line Therapy and the Basis of Personality. Meta Publications, Cupertino, CA, 1988

11. Metcalfe, D. D. Mast cell mediators with emphasis on intestinal mast cells. Annals of Allergy 53:563-575, 1984

12. Farnam, J., Grant, J. A. Angioedema. Dermatologic Clinics 3:85-95, 1985

13. Wasserman, S. I. Basic Mechanisms in asthma. Annals of Allergy 60:477-482, 1988

14. Khan, A. U., Bonk, C., Gordon, Y. Non-allergic asthma and conditioning process. Annals of Allergy 32:245-251, 1974

15. Khan, A. U. Effectiveness of biofeedback and counter-conditioning in the treatment of bronchial asthma. Journal of Psychosomatic Research 21:97-104, 1977

16. MacQueen, G., Marshall, J., Perdue, M., Siegel, S., Bienenstock, J. Pavlovian conditioning of rat mucosal mast cells to secrete rat mast cell protease II. Science 243:83-5, 1989.

17. Russell, M., et al. Learned histamine release. Science 225:773-734, 1984

18. Hall, S. Biochemical codes: the language of life? Smithsonian 20:62-71, 1989

19. Hagermark, O., Hokfelt, T., Pernow, B. Flare and itch induced by substance P in human skin. Journal of Investigative Dermatology 71:233-235, 1978

20. Foreman, J. C., Jordan, C. C., Piotrowski, W. Interaction of neurotensin with the substance P receptor mediating histamine release from rat mast cells and the flare in human skin. British Journal of Pharmacology 77:531-539, 1982

21. Jozaki, K. Kuriu, A., Waki, N., Adachi, S., Yamatodani, A., Tarui, S., Kitamura, Y. Proliferative potential of murine peritoneal mast cells after degranulation induced by compound 48/80, substance P, tetradecanoylphorbol acetate, or calcium ionophore A23187. Journal of Immunology 145:4252-4256, 1990

22. Caulfield, J. P., el-Lati, S., Thomas, G., Church, M. K., Dissociated human foreskin mast cells degranulate in response to anti-IgE and substance P. Laboratory Investigation 63:502-10, 1990

23. Irman-Florjanc, T., Erjavec, F. The effect of adrenocorticotropin on histamine and 5-hydroxytryptamine secretion from rat mast cells. Agents and Actions 14:454-457, 1984

24. Sugiyama, K., Furuta, H., Histamine release induced by dynorphin-(1-13) from rat mast cells. Japanese Journal of Pharmacology 35:247-252, 1984

25. Batchelor, K. W., Stanworth, D. R. A comparison of the histamine-releasing properties of rat pleural and peritoneal mast cells. Immunology 41:271-278, 1980

26. Casale, T. B., Bowman, S., Kaliner, M. Induction of human cutaneous mast cell degranulation by opiates and endogenous opioid peptides: evidence for opiate and nonopiate receptor participation. Journal of Allergy and Clinical Immunology 73:775-781, 1984

27. Guillemin, R., Vargo, T., Rossier, J., Minick, S., Ling, N., Rivier, C., Vale W., Bloom F. beta-Endorphin and adrenocorticotropin are selected concomitantly by the pituitary gland. Science 197:1367-1369, 1977

28. Jankovic, B. D., Maric, D. Enkephalins and anaphylactic shock: modulation and prevention of shock in the rat. Immunology Letters 15:153-160, 1987

29. Weihe, E., Nohr, D., Michel, S., Muller, S., Zentel, H.-J., Fink, T., Krekel, J. Molecular anatomy of the neuro-immune connection. International Journal of Neuroscience 59:1, 1991

30. Weihe, E., Neuropeptides in primary afferent neurons. In: The Primary Afferent Neuron- a survey of recent morpho-functional aspects. Zenker, W. and Neuhuber, W. L., eds. Plenum Press, New York, pp. 127-159, 1990

31. Amir, S., van Ree, J. M. Beneficial effect of gamma-endorphin-type peptides in anaphylactic shock. Brain Research 329:329-333, 1985

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