Immunophenotypic assessment of PNH clones in major and minor cell lineages in the peripheral blood of patients with paroxysmal nocturnal hemoglobinuria
Author:
Affiliation:
1. Division of Haematology and Immunology, Leeds Institute of Medical Research at St James's University of Leeds Leeds UK
2. Haematological Malignancy Diagnostic Service, Leeds Teaching Hospitals NHS Trust St. James's University Hospital Leeds UK
Publisher
Wiley
Subject
Cell Biology,Histology,Pathology and Forensic Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cyto.b.22094
Reference26 articles.
1. Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency
2. Guidelines for the diagnosis and monitoring of paroxysmal nocturnal hemoglobinuria and related disorders by flow cytometry;Borowitz M. J.;Cytometry. Part B, Clinical Cytometry,2010
3. Flow cytometric diagnosis of paroxysmal nocturnal hemoglobinuria: Pearls and Pitfalls – A critical review article;Brando B.;EJIFCC,2019
4. Features, reason for testing, and changes with time of 583 paroxysmal nocturnal hemoglobinuria clones from 529 patients: a multicenter Italian study
5. ICCS/ESCCA Consensus Guidelines to detect GPI-deficient cells in Paroxysmal Nocturnal Hemoglobinuria (PNH) and related Disorders Part 1 - Clinical Utility
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