Guidelines on red cell transfusion in sickle cell disease. Part I: principles and laboratory aspects-Reference-Cited by-同舟云学术

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Guidelines on red cell transfusion in sickle cell disease. Part I: principles and laboratory aspects

Published:2016-11-07 Issue:2 Volume:176 Page:179-191
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Davis Bernard A.¹,Allard Shubha²,Qureshi Amrana³,Porter John B.⁴,Pancham Shivan⁵,Win Nay⁶,Cho Gavin⁶,Ryan Kate⁷,

Affiliation:

1. Whittington Health; London UK

2. Barts Health NHS Trust & NHS Blood and Transplant; London UK

3. Oxford University Hospitals NHS Foundation Trust; Oxford UK

4. University College London Hospitals NHS Foundation Trust; London UK

5. Sandwell and West Birmingham Hospitals NHS Trust; Birmingham UK

6. NHS Blood and Transplant; London UK

7. Central Manchester University Hospitals NHS Foundation Trust; Manchester UK

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.14346/fullpdf

Reference102 articles.

1. Discontinuing prophylactic transfusions used to prevent stroke in sickle cell disease;Adams;New England Journal of Medicine,2005

2. Erythrocytapheresis can reduce iron overload and reduce the need for chelation therapy in chronically transfused pediatric patients;Adams;Journal of Pediatric Hematology/oncology,1996

3. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography;Adams;The New England Journal of Medicine,1998

4. Rheologic behavior of sickle and normal red blood cell mixtures in sickle plasma: implications for transfusion therapy;Alexy;Transfusion,2006

5. Complications of PORT-A-CATH(R) in patients with sickle cell disease;Alkindi;Journal of Infection and Public Health,2012

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