Dysplasia and PNH ‐type cells in bone marrow aspirates of myelodysplastic syndromes

Author:

Westers Theresia M.1,Alhan Canan1,Visser‐Wisselaar Heleen A.2,Chitu Dana A.2,Loosdrecht Arjan A.1

Affiliation:

1. Department of Hematology Amsterdam University Medical Centers, Location VU University Medical Center, Cancer Center Amsterdam Amsterdam The Netherlands

2. Department of Hematology HOVON Data Center, Erasmus MC Cancer Institute Rotterdam The Netherlands

Publisher

Wiley

Subject

Cell Biology,Histology,Pathology and Forensic Medicine

Reference35 articles.

1. 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

2. Flow cytometric diagnosis of paroxysmal nocturnal hemoglobinuria: Pearls and pitfalls—A critical review article;Brando B.;EJIFCC,2019

3. Implementation of erythroid lineage analysis by flow cytometry in diagnostic models for myelodysplastic syndromes

4. Neutrophil Fc gamma RIIIb deficiency, nature, and clinical consequences: a study of 21 individuals from 14 families

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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