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2. Erythrocyte membrane protein deficiencies in paroxysmal nocturnal hemoglobinuria. Schultz DR Am J Med; 1989 Sep; 87(3N):22N-29N. PubMed ID: 2484793 [TBL] [Abstract][Full Text] [Related]
3. [Current theories on the pathogenesis and treatment of nocturnal paroxysmal hemoglobinuria (NPH)]. Robak T Przegl Lek; 1990; 47(11):763-6. PubMed ID: 1711705 [No Abstract] [Full Text] [Related]
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5. Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria. Yamashina M; Ueda E; Kinoshita T; Takami T; Ojima A; Ono H; Tanaka H; Kondo N; Orii T; Okada N N Engl J Med; 1990 Oct; 323(17):1184-9. PubMed ID: 1699124 [No Abstract] [Full Text] [Related]
6. Deficiency of phosphatidylinositol-linked membrane proteins on erythrocytes of different subpopulations in paroxysmal nocturnal hemoglobinuria. Cui Y; Zhang ZN; Liu EK; Pan HZ Chin Med J (Engl); 1993 May; 106(5):323-30. PubMed ID: 7691484 [TBL] [Abstract][Full Text] [Related]
14. Paroxysmal nocturnal hemoglobinuria type III. Lack of an erythrocyte membrane protein restricting the lysis by C5b-9. Hänsch GM; Schönermark S; Roelcke D J Clin Invest; 1987 Jul; 80(1):7-12. PubMed ID: 3597779 [TBL] [Abstract][Full Text] [Related]
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16. Application of flow cytometry to the diagnosis of paroxysmal nocturnal hemoglobinuria. Richards SJ; Rawstron AC; Hillmen P Cytometry; 2000 Aug; 42(4):223-33. PubMed ID: 10934341 [TBL] [Abstract][Full Text] [Related]