Abnormalities in the expression of CD55 and CD59 surface molecules on peripheral blood cells are not specific to paroxysmal nocturnal hemoglobinuria

By Ruiz-Delgado Guillermo J.   Vázquez-Garza Eduardo   Méndez-Ramírez Nereida   Gómez-Almaguer David  

Hematology, Vol. 14, Iss. 1, 2009-02 ,pp. : 33-37

Maney Publishing

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Defective TCR signaling events in glycosylphosphatidylinositol-deficient T cells derived from paroxysmal nocturnal hemoglobinuria patients

By Romagnoli P.   Bron C.  

International Immunology, Vol. 11, Iss. 9, 1999-09 ,pp. : 1411-1422

Oxford University Press

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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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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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