Transfusion and Chelation Practices in Sickle Cell Disease: A Regional Perspective-Reference-Cited by-同舟云学术

Transfusion and Chelation Practices in Sickle Cell Disease: A Regional Perspective

Published:2010-07-30 Issue:2 Volume:28 Page:124-133
ISSN:0888-0018
Container-title:Pediatric Hematology and Oncology
language:en
Short-container-title:Pediatric Hematology and Oncology

Author:

Vichinsky Chairs Elliott P.,Ohene-Frempong Kwaku,Thein Regional Chairs Swee Lay,Lopes de Castro Lobo Clarisse,Inati Adlette,Thompson Alexis A.,Smith-Whitley Other Faculty Kim,Kwiatkowski Janet L.,Swerdlow Paul S.,Porter John B.,Marks Peter W.

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.3109/08880018.2010.505506

Reference20 articles.

1. Effect of Hydroxyurea on the Frequency of Painful Crises in Sickle Cell Anemia

2. Iron overload is a determinant of morbidity and mortality in adult patients with sickle cell disease

3. Collaborative Data Project [C-DATA] of the Comprehensive Sickle Cell Centers Program.

4. Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusions

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