Red blood cell reduction of a sickle cell disease stem cell product
Author:
Affiliation:
1. Department of Pathology and Cell Biology Columbia University Irving Medical Center New York New York USA
2. NewYork‐Presbyterian Hospital New York New York USA
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.16633
Reference6 articles.
1. Successful hematopoietic stem cell mobilization and apheresis collection using plerixafor alone in sickle cell patients
2. Poor stem cell harvest may not always be related to poor mobilization: lessons gained from a mobilization study in patients with β-thalassemia major
3. Harvesting autologous stem cells from a patient with red blood cell abnormalities of β-thalassemia intermedia
4. Hematopoietic Stem Cell Mobilization for Gene Therapy: Superior Mobilization by the Combination of Granulocyte–Colony Stimulating Factor Plus Plerixafor in Patients with β-Thalassemia Major
5. Hematopoietic Stem Cell Mobilization for Gene Therapy of Adult Patients With Severe β-Thalassemia: Results of Clinical Trials Using G-CSF or Plerixafor in Splenectomized and Nonsplenectomized Subjects
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