Case series of octogenarians with sickle cell disease

Author:

Ballas Samir K.1ORCID,Pulte E. Dianne1,Lobo Clarisse2,Riddick-Burden Gaye3

Affiliation:

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

2. Clinical Hematology Division, Instituto Estadual de Hematologia Arthur de Siqueira Cavalcanti, Rio de Janeiro, Brazil; and

3. Department of Nursing, Thomas Jefferson University, Philadelphia, PA

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference16 articles.

1. Mortality in sickle cell disease: life expectancy and risk factors for early death.;Platt;N Engl J Med,1994

2. The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: a 17.5 year follow-up.;Steinberg;Am J Hematol,2010

3. Survival estimates for patients with homozygous sickle-cell disease in Jamaica: a clinic-based population study.;Wierenga;Lancet,2001

4. Survival among children and adults with sickle cell disease in Belgium: benefit from hydroxyurea treatment.;Lê;Pediatr Blood Cancer,2015

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