ICCS/ESCCA Consensus Guidelines to detect GPI-deficient cells in Paroxysmal Nocturnal Hemoglobinuria (PNH) and related Disorders Part 1 - Clinical Utility
Author:
Affiliation:
1. Department of Oncology; Johns Hopkins Medical Institutions; Baltimore Maryland
2. Department of Pathology; Johns Hopkins Medical Institutions; Baltimore Maryland
Publisher
Wiley
Subject
Cell Biology,Histology,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/cyto.b.21608/fullpdf
Reference19 articles.
1. How I treat paroxysmal nocturnal hemoglobinuria;Brodsky;Blood,2009
2. Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin;Brodsky;Am J Clin Pathol,2000
3. Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. I. The sensitivity of PNH red cells to lysis by complement and specific antibody;Rosse;J Clin Invest,1966
4. The life-span of complement-sensitive and -insensitive red cells in paroxysmal nocturnal hemoglobinuria;Rosse;Blood,1971
5. Deficiency of glycosyl-phosphatidylinositol-linked membrane glycoproteins of leukocytes in paroxysmal nocturnal hemoglobinuria, Description of a new diagnostic cytoflourometric assay;Vanderschoot;Blood,1990
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