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Paroxysmal nocturnal haemoglobinuria

Selvaraj, P., Rosse, W. F., Silber, R., Springer, T. A. (1988). The major Fc receptor in blood has a phosphatidylinositol anchor and is deficient in paroxysmal nocturnal haemoglobinuria. Nature 333,565-7. [Pg.126]

Goldstein, B. D. Production of paroxysmal nocturnal haemoglobinuria-like red cells by reducing the oxidizing agents. Brit. J. Haematol. 26 49-58, 1974. [Pg.380]

Simak J, Holada K, Risitano AM, Zivny JH, Young NS, Vostal JG. Elevated circulating endothelial membrane microparticles in paroxysmal nocturnal haemoglobinuria. Br J Haematol 2004 125 804-813. [Pg.158]

Ronne E, Pappot H, Grondahl-Hansen J, Hoyer-Hansen G, Plesner T, Hansen NE, et al. The receptor for urokinase plasminogen activator is present in plasma from healthy donors and elevated in patients with paroxysmal nocturnal haemoglobinuria. Br J Haematol 1995 89(3) 576-581. [Pg.99]

Numerous congenital or acquired diseases lead to haemolysis, (s. p. 218) (s. tab. 12.3) They are subsumed under the term haemolytic syndrome. Particularly, sickle-cell anaemia, thalassaemia and paroxysmal nocturnal haemoglobinuria are worthy of mention in this context. [Pg.814]

Rosse, W.F. Paroxysmal nocturnal haemoglobinuria as a molecular disease. Medicine 1997 76 63—93... [Pg.821]

Lupus anticoagulant Myeloproliferative disease (31) Paroxysmal nocturnal haemoglobinuria Polycythaemia vera Protein C deficiency (68)... [Pg.831]

Paroxysmal nocturnal haemoglobinuria Sickle cell anaemia ... [Pg.836]

See other pages where Paroxysmal nocturnal haemoglobinuria is mentioned: [Pg.118]    [Pg.317]    [Pg.675]    [Pg.82]    [Pg.814]    [Pg.2286]    [Pg.150]    [Pg.66]    [Pg.66]    [Pg.150]    [Pg.1543]    [Pg.118]    [Pg.317]    [Pg.675]    [Pg.82]    [Pg.814]    [Pg.2286]    [Pg.150]    [Pg.66]    [Pg.66]    [Pg.150]    [Pg.1543]   
See also in sourсe #XX -- [ Pg.270 ]



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Haemoglobinuria

Nocturnal

Nocturne

Paroxysmal nocturnal

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