CameronG. R.FinckhE. S. (1956). The production of an acute haemolytic crisis by the subcutaneous injection of glycerol. J. Path. Bact., 71, 165.
2.
DelormeE. J. (1952). Experimental cooling of blood stream. Lancet, 2, 914.
3.
FeldbergW.TalesnikJ. (1953). Reduction of tissue histamine by Compound 48/80. J. Physiol. (Lond.), 120, 550.
4.
FrankH. A.FineJ. (1943). Traumatic shock V: A study of the effect of oxygen on haemorrhagic shock. J. clin. Invest., 22, 305.
5.
FrankH. A.JacobsS. W.SchweinburgF. B.GoddardJ.FineJ. (1952). Traumatic shock XXI: effectiveness of an antibiotic in experimental haemorrhagic shock. Amer. J. Physiol., 168, 430.
6.
FrankH. A.SeligmanA. M.FineJ. (1946). Traumatic shock XIII: The prevention of irreversibility in haemorrhagic shock by viviperfusion of the liver. J. clin. Invest., 25, 22.
7.
HayE. B.WebbK. W. (1951). The effect of increased arterial blood flow to the liver on the mortality rate following haemorrhagic shock. Surgery, 29, 826.
8.
NobleR. L.CollipJ. B. (1942). A quantitative method for production of experimental shock without haemorrhage in unanaesthetised animals. Quart. J. exp. Physiol., 31, 187.
9.
SchnedorfJ. G.OrrT. G. (1941). Oxygen therapy in shock due to haemorrhage. Surg. Gynec. Obstet., 73, 495.