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Pediatric Blood & Cancer
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July 19, 2019
Characterizing complication risk from multisite, intermittent transfusions for the treatment of sickle cell disease
Amy Tang, Jane Branscomb, Mei Zhou, et al.
American Journal of Hematology
|
September 28, 2010
Leg ulcers in sickle cell disease
Caterina P Minniti, James Eckman, Paola Sebastiani, et al.
Public Health Reports (Washington, D.C. : 1974)
|
April 11, 2019
Improving an Administrative Case Definition for Longitudinal Surveillance of Sickle Cell Disease
Angela B Snyder, Mei Zhou, Rodney Theodore, et al.
Pediatric Blood & Cancer
|
May 4, 2024
Immunization adherence among children with sickle cell disease and sickle cell trait: Results of a population-based study
Jiajing Scarlette Shi, Ankit Sutaria, Sangeetha Lakshmanan, et al.
Contemporary Clinical Trials
|
January 20, 2023
Sickle Cell Trevor Thompson Transition Project (ST3P-UP) protocol for managing care transitions: Methods and rationale
Ifeyinwa Osunkwo, Raymona Lawrence, Myra Robinson, et al.
American Journal of Hematology
|
November 21, 2008
Sickle cell disease summit: from clinical and research disparity to action
Kathryn Hassell, Betty Pace, Winfred Wang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 11, 2002
Feasibility and correlates of arsenic trioxide combined with ascorbic acid-mediated depletion of intracellular glutathione for the treatment of relapsed/refractory multiple myeloma
Nizar J Bahlis, Jennifer McCafferty-Grad, Ileana Jordan-McMurry, et al.
British Journal of Haematology
|
January 20, 2007
A randomised comparison of deferasirox versus deferoxamine for the treatment of transfusional iron overload in sickle cell disease
Elliott Vichinsky, Onyinye Onyekwere, John Porter, et al.
JAMA
|
April 4, 2003
Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment
Martin H Steinberg, Franca Barton, Oswaldo Castro, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Pediatric Blood & Cancer
|
July 19, 2019
Characterizing complication risk from multisite, intermittent transfusions for the treatment of sickle cell disease
Amy Tang, Jane Branscomb, Mei Zhou, et al.
American Journal of Hematology
|
September 28, 2010
Leg ulcers in sickle cell disease
Caterina P Minniti, James Eckman, Paola Sebastiani, et al.
Public Health Reports (Washington, D.C. : 1974)
|
April 11, 2019
Improving an Administrative Case Definition for Longitudinal Surveillance of Sickle Cell Disease
Angela B Snyder, Mei Zhou, Rodney Theodore, et al.
Pediatric Blood & Cancer
|
May 4, 2024
Immunization adherence among children with sickle cell disease and sickle cell trait: Results of a population-based study
Jiajing Scarlette Shi, Ankit Sutaria, Sangeetha Lakshmanan, et al.
Contemporary Clinical Trials
|
January 20, 2023
Sickle Cell Trevor Thompson Transition Project (ST3P-UP) protocol for managing care transitions: Methods and rationale
Ifeyinwa Osunkwo, Raymona Lawrence, Myra Robinson, et al.
American Journal of Hematology
|
November 21, 2008
Sickle cell disease summit: from clinical and research disparity to action
Kathryn Hassell, Betty Pace, Winfred Wang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 11, 2002
Feasibility and correlates of arsenic trioxide combined with ascorbic acid-mediated depletion of intracellular glutathione for the treatment of relapsed/refractory multiple myeloma
Nizar J Bahlis, Jennifer McCafferty-Grad, Ileana Jordan-McMurry, et al.
British Journal of Haematology
|
January 20, 2007
A randomised comparison of deferasirox versus deferoxamine for the treatment of transfusional iron overload in sickle cell disease
Elliott Vichinsky, Onyinye Onyekwere, John Porter, et al.
JAMA
|
April 4, 2003
Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment
Martin H Steinberg, Franca Barton, Oswaldo Castro, et al.
Page
of 1