Physiopathologie de l'hémoglobinurie paroxystique nocturne

Author:

de Gramont A

Publisher

Elsevier BV

Subject

Gastroenterology,Internal Medicine

Reference14 articles.

1. Chronic hemolytic anemia with paroxysmal hemoglobinuria. Study of the mechanism of hemolysis in relation to acid-base equilibrium;Ham;N Engl J Med,1937

2. Proxysmal nocturnal hemoglobinuria. Alternate-complement-pathway-mediated lysis induced by magnesium;May;N Engl J Med,1973

3. Affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria are deficient in the complement regulatory protein, decay accelerating factor;Nicholson-Weller,1983

4. The population of paroxysmal nocturnal hemoglobinuria neutrophils deficient in decay-accelerating factor is also deficient in alkaline phosphatase;Burroughs;Blood,1988

5. Synthesis of mannosylglucosaminylinositol phospholipids in normal and paroxysmal nocturnal hemoglobinuria cells;Hirose,1992

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