From total blood exchange to erythrocytapheresis and back to treat complications of sickle cell disease-Reference-Cited by-同舟云学术

From total blood exchange to erythrocytapheresis and back to treat complications of sickle cell disease

Published:2017-05-03 Issue:9 Volume:57 Page:2277-2280
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Ballas Samir K.¹

Affiliation:

1. Cardeza Foundation for Hematologic Research, Department of Medicine; Sidney Kimmel Medical College, Thomas Jefferson University; Philadelphia Pennsylvania

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/trf.14154/fullpdf

Reference23 articles.

1. Guidelines on the use of therapeutic apheresis in clinical practice-evidence-based approach from the Writing Committee of the American Society for Apheresis: the seventh special issue;Schwartz;J Clin Apher,2016

2. Comparison of automated erythrocytapheresis versus manual exchange transfusion to treat cerebral macrovasculopathy in sickle cell anemia;Koehl;Transfusion,2016

3. From individualized treatment of sickle cell pain to precision medicine: a 40-year journey;Ballas;J Clin Med Res,2016

4. RBC exchange pheresis for priapism in sickle cell disease;Rifkind;JAMA,1979

5. Exchange red blood cell pheresis in a pediatric patient with severe complications of sickle cell anemia;Kleinman;Transfusion,1981

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1. A comparison between erythrocytapheresis and venesection for the treatment of JAK2‐mutated polycythaemia;Internal Medicine Journal;2023-12-25

2. Comprehensive guide to managing a chronic automated red cell exchange program in sickle cell disease;Journal of Clinical Apheresis;2022-09-29

3. Antioxidant-Rich Nutraceutical as a Therapeutic Strategy for Sickle Cell Disease;Journal of the American Nutrition Association;2022-09-07

4. Red blood cells modulate structure and dynamics of venous clot formation in sickle cell disease;Blood;2019-06-06

5. Transfusion‐transmitted malaria masquerading as sickle cell crisis with multisystem organ failure;Transfusion;2018-03-09