CD34 + cells from paroxysmal nocturnal hemoglobinuria (PNH) patients are deficient in surface expression of cellular prion protein (PrP c )

By Risitano A.M.   Holada K.   Chen G.   Simak J.   Vostal J.G.   Young N.S.   Maciejewski J.P.  

Experimental Hematology, Vol. 31, Iss. 1, 2003-01 ,pp. : 65-72

Elsevier

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Granulocytes from patients with paroxysmal nocturnal hemoglobinuria and normal individuals have the same sensitivity to spontaneous apoptosis

By Yamamoto T.   Shichishima T.   Shikama Y.   Saitoh Y.   Ogawa K.   Maruyama Y.  

Experimental Hematology, Vol. 30, Iss. 3, 2002-03 ,pp. : 187-194

Elsevier

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Clinical signs and symptoms associated with increased risk for thrombosis in patients with paroxysmal nocturnal hemoglobinuria from a Korean Registry

By Lee Jong  

International Journal of Hematology, Vol. 97, Iss. 6, 2013-06 ,pp. : 749-757

Springer Publishing Company

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New insights into paroxysmal nocturnal hemoglobinuria

By Savage William J.   Brodsky Robert A.  

Hematology, Vol. 12, Iss. 5, 2007-10 ,pp. : 371-376

Maney Publishing

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Clinical paroxysmal nocturnal hemoglobinuria is the result of expansion of glycosyl-phosphatidyl-inositol-anchored protein-deficient clone in the condition of Deficient Hematopoiesis

By Pakdeesuwan Kriangsak   Muangsup Wanna   U-Pratya Yaowalak   Issaragrisil Surapol   Wanachiwanawin Wanchai  

International Journal of Hematology, Vol. 73, Iss. 1, 2001-01 ,pp. : 64-70

Springer Publishing Company

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