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Original Article

The Effect of Muscular Exercise on Hemostasis in Von Willebrand's Disease

Pages 273-283 | Received 01 Feb 1963, Published online: 13 May 2010

References

  • Alexander B., Goldstein R. Dual hemostatic defect in pseudohemophilia. J. clin. Invest. 1953; 32: 531
  • Borchgrevink C. F., Egeberg O., Godal H. C., Hjort P. F. The effect of plasma and Cohn's fraction I on the Duke and Ivy bleeding rime in von Willebrand's disease. Acta med. scand. 1963; 173: 235
  • Alexander B., Waaler B. A. The secondary bleeding time. Ibid. 1958; 162: 361
  • Egeberg O. Assay of antihemophilic A, B and C factors by one-stage cephalin systems. Scand. J. clin. Lab. Invest. 1961; 13: 140
  • Burstein M., Guinand A. Antihemophilic A factor (factor VIII) and fibrinogen in human blood. A study on the question of a closer correlation between the levels of the two factors. Ibid. 1962; 14: 230
  • Burstein M., Guinand A. The effect of unspecific fever induction on the blood clotting system. Ibid. 1962; 14: 471
  • Turpeinen O. The effect of exercise on the blood clotting system. Ibid. 1963; 15: 8
  • Burstein M., Guinand A. Influence of thyroid function on the blood clotting system. Ibid. 1963; 15: 1
  • Graham J. B. The inheritance of “vascular hemophilia”. A new and interesting problem in human genetics. Amer. J. hum. Genet. 1959; 11: 385
  • Hjort P. F. Intermediate reactions in the coagulation of blood with tissue thromboplastin. Ibid. 1957; 9
  • Rapaport S. I., Owren P. A. A simple one-stage prothrombin assay using Russell's viper venom in cephalin suspension. J. Lab. din. med. 1955; 46: 89
  • Ingram G. I. C. Increase in antihaemophilic globulin activity following infusion of adrenaline. J. Physiol. 1961; 156: 217
  • Ivy A. C., Nelson D., Bucher G. The standardization of certain factors in the cutaneous “venestasis” bleeding time technique. J. Lab. din. Med. 1941; 26: 1812
  • Jiirgens R., Lehman W., Wegelius O., Eriksson A. W., Hiepler E. Mitteilung iiber den Mangel an antihamophilischen Globulin (Fak-tor VIII) bei der Aalandischen Thrombo-pathie (v. Willebrand—Jürgens). Thromb. Diathes. haemorrh. (Stuttg.) 1957; 1: 257
  • Larrieu M. J., Soulier J. P. Deficit en facteur antihémophilique A chez une fille associé a un trouble du saignement. Rev. Hémat. 1953; 8: 361
  • Nilsson I. M., Blombäck M., Blombäck B. Von Willebrand's disease in Sweden. Its pathogenesis and treatment. Acta med. scand. 1959; 164: 263
  • Blombäck M., von Francken I. On an inherited autosomal hemorrhagic diathesis with antihemophilic globulin (AHG) deficiency and prolonged bleeding time. Ibid. 1957; 159: 35
  • Quick A. J., Hussey C. V. Hemophilic condition in the female. J. Lab. clin. Med. 1953; 42: 929
  • Rizza C. R. Effect of exercise on the level of antihaemophilic globulin in human blood. J. Physiol. 1961; 156: 128
  • Von Willebrand E. A. Über hereditäre Pseudo-hämophilie. Acta med. scand. 1931; 76: 52
  • Mason M. F., Hawley G., Jürgens R. Über eine neues vererbares Blutungsübel: Die konstitutionelle Thrombo-pathie. Dtsch. Arch. klin. Med. 1933; 175: 453
  • Waaler B. A. Contact activation in the intrinsic blood clotting system. Studies on a plasma product formed on contact with glass and similar surfaces. Scand. J. din. Lab. Invest. 1959; 11

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