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

International Journal of Hematology

Volumn 73, Issue 1, 2001, Pages 64-70

  Pakdeesuwan, Kriangsak ^a   Muangsup, Wanna ^a   U Pratya, Yaowalak ^a   Issaragrisil, Surapol ^a   Wanachiwanawin, Wanchai ^a  

^a MAHIDOL UNIVERSITY   (Thailand)

Author keywords

CD34+ cells; GPI proteins; Hematopoiesis; Paroxysmal nocturnal hemoglobinuria

Indexed keywords

CD34 ANTIGEN; CD59 ANTIGEN; GLYCOSYLPHOSPHATIDYLINOSITOL; MEMBRANE PROTEIN; PHOSPHATIDYLINOSITOL GLYCAN CLASS A PROTEIN; PHOSPHATIDYLINOSITOL GLYCAN-CLASS A PROTEIN;

ADULT; AGED; ARTICLE; BIOSYNTHESIS; BLOOD; CASE CONTROL STUDY; CELL CLONE; CHEMISTRY; CYTOLOGY; FEMALE; GENETICS; HEMATOPOIESIS; HUMAN; IMMUNOLOGY; MALE; MIDDLE AGED; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PATHOLOGY; PHYSIOLOGY; RETICULOCYTE; STEM CELL;

ADULT; AGED; ANTIGENS, CD34; ANTIGENS, CD59; CASE-CONTROL STUDIES; CLONE CELLS; FEMALE; GLYCOSYLPHOSPHATIDYLINOSITOLS; HEMATOPOIESIS; HEMOGLOBINURIA, PAROXYSMAL; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; RETICULOCYTES; STEM CELLS;

EID: 0035237212     PISSN: 09255710     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02981904     Document Type: Article

References (2)

1. Dacie JV, Lewis SM. Paroxysmal nocturnal haemoglobinuria: clinical manifestations, hematology and nature of the disease. Ser Hematol. 1972;3:3-22.
2. Rosse WE Paroxysmal nocturnal hemoglobinuria as a molecular disease. Medicine (Baltimore). 1997;76:63-94.