ICCS/ESCCA Consensus Guidelines to detect GPI-deficient cells in Paroxysmal Nocturnal Hemoglobinuria (PNH) and related Disorders Part 3 - Data Analysis, Reporting and Case Studies-Reference-Cited by-同舟云学术

ICCS/ESCCA Consensus Guidelines to detect GPI-deficient cells in Paroxysmal Nocturnal Hemoglobinuria (PNH) and related Disorders Part 3 - Data Analysis, Reporting and Case Studies

Published:2018-01 Issue:1 Volume:94 Page:49-66
ISSN:1552-4949
Container-title:Cytometry Part B: Clinical Cytometry
language:en
Short-container-title:Cytometry

Author:

Illingworth Andrea¹,Marinov Iuri²,Sutherland D. Robert³,Wagner-Ballon Orianne⁴,DelVecchio Luigi⁵

Affiliation:

1. Dahl-Chase Diagnostic Services in Bangor; Maine USA

2. Institute of Hematology and Blood Transfusion; Prague Czech Republic

3. Laboratory Medicine Program; Toronto General Hospital; Toronto Canada

4. Département d'Hématologie et d'Immunologie Biologiques Hôpital Henri Mondor; Créteil France

5. Federico II University and CEINGE Institute in Naples; Naples Italy

Publisher

Wiley

Subject

Cell Biology,Histology,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/cyto.b.21609/fullpdf

Reference25 articles.

1. The molecular basis of paroxysmal nocturnal hemoglobinuria;Rosse;Blood,1995

2. Historical aspects of paroxysmal nocturnal haemoglobinuria: ‘Defining the disease;Parker;Br J Haematol,2002

3. Natural history of paroxysmal nocturnal hemoglobinuria;Hillmen;N Engl J Med,1995

4. Deficiency of glycosyl-phosphatidylinositol-linked membrane glycoproteins of leukocytes in paroxysmal nocturnal hemoglobinuria, description of a new diagnostic cytofluorometric assay;Schoot;Blood,1990

5. The use of monoclonal antibodies and flow cytometry in the diagnosis of paroxysmal nocturnal hemoglobinuria;Hall;Blood,1996

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