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Clinicoeconomics and Outcomes Research : CEOR
|
November 5, 2020
Development of a Severity Classification System for Sickle Cell Disease
Nirmish Shah, David Beenhouwer, Michael S Broder, et al.
The Journal of Pain
|
August 6, 2023
Biopsychosocial Factors Associated With Pain and Pain-Related Outcomes in Adults and Children With Sickle Cell Disease: A Multivariable Analysis of the GRNDaD Multicenter Registry
Martha O Kenney, Samuel Wilson, Nirmish Shah, et al.
The Journal of Clinical Investigation
|
February 27, 2025
Megakaryocytes transfer mitochondria to bone marrow mesenchymal stromal cells to lower platelet activation
Chengjie Gao, Yitian Dai, Paul A Spezza, et al.
Pediatric Blood & Cancer
|
October 18, 2024
Prevent Acute Chest Syndrome checklist (PACScheck): A quality improvement initiative to reduce acute chest syndrome
Kerry Morrone, Kaitlin Strumph, Catherine Pisacano, et al.
Plos One
|
April 6, 2012
Therapeutic hemoglobin levels after gene transfer in β-thalassemia mice and in hematopoietic cells of β-thalassemia and sickle cells disease patients
Laura Breda, Carla Casu, Sara Gardenghi, et al.
British Journal of Haematology
|
August 23, 2021
Gaps in the diagnosis and management of iron overload in sickle cell disease: a 'real-world' report from the GRNDaD registry
Samuel R Wilson, Matthew Sears, Elizabeth Williams, et al.
British Journal of Haematology
|
March 16, 2021
Vasculo-toxic and pro-inflammatory action of unbound haemoglobin, haem and iron in transfusion-dependent patients with haemolytic anaemias
Francesca Vinchi, Richard Sparla, Sara T Passos, et al.
Journal of Racial and Ethnic Health Disparities
|
May 18, 2020
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research
Andrew D Campbell, Raffaella Colombatti, Biree Andemariam, et al.
JAMA Network Open
|
November 13, 2025
National Alliance of Sickle Cell Centers Consensus Recommendations on Sickle Cell Disease Health Maintenance: A Consensus Statement
Seethal A Jacob, Melissa Frei-Jones, Sana Saif-Ur-Rehman, et al.
Haematologica
|
May 23, 2020
2'-O-methoxyethyl splice-switching oligos correct splicing from IVS2-745 β-thalassemia patient cells restoring HbA production and chain rebalance
Alisa Dong, Valentina Ghiaccio, Irene Motta, et al.
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Search research articles
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Showing results (121-130 of 138) with videos related to
Sort By:
Page
of 14
Clinicoeconomics and Outcomes Research : CEOR
|
November 5, 2020
Development of a Severity Classification System for Sickle Cell Disease
Nirmish Shah, David Beenhouwer, Michael S Broder, et al.
The Journal of Pain
|
August 6, 2023
Biopsychosocial Factors Associated With Pain and Pain-Related Outcomes in Adults and Children With Sickle Cell Disease: A Multivariable Analysis of the GRNDaD Multicenter Registry
Martha O Kenney, Samuel Wilson, Nirmish Shah, et al.
The Journal of Clinical Investigation
|
February 27, 2025
Megakaryocytes transfer mitochondria to bone marrow mesenchymal stromal cells to lower platelet activation
Chengjie Gao, Yitian Dai, Paul A Spezza, et al.
Pediatric Blood & Cancer
|
October 18, 2024
Prevent Acute Chest Syndrome checklist (PACScheck): A quality improvement initiative to reduce acute chest syndrome
Kerry Morrone, Kaitlin Strumph, Catherine Pisacano, et al.
Plos One
|
April 6, 2012
Therapeutic hemoglobin levels after gene transfer in β-thalassemia mice and in hematopoietic cells of β-thalassemia and sickle cells disease patients
Laura Breda, Carla Casu, Sara Gardenghi, et al.
British Journal of Haematology
|
August 23, 2021
Gaps in the diagnosis and management of iron overload in sickle cell disease: a 'real-world' report from the GRNDaD registry
Samuel R Wilson, Matthew Sears, Elizabeth Williams, et al.
British Journal of Haematology
|
March 16, 2021
Vasculo-toxic and pro-inflammatory action of unbound haemoglobin, haem and iron in transfusion-dependent patients with haemolytic anaemias
Francesca Vinchi, Richard Sparla, Sara T Passos, et al.
Journal of Racial and Ethnic Health Disparities
|
May 18, 2020
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research
Andrew D Campbell, Raffaella Colombatti, Biree Andemariam, et al.
JAMA Network Open
|
November 13, 2025
National Alliance of Sickle Cell Centers Consensus Recommendations on Sickle Cell Disease Health Maintenance: A Consensus Statement
Seethal A Jacob, Melissa Frei-Jones, Sana Saif-Ur-Rehman, et al.
Haematologica
|
May 23, 2020
2'-O-methoxyethyl splice-switching oligos correct splicing from IVS2-745 β-thalassemia patient cells restoring HbA production and chain rebalance
Alisa Dong, Valentina Ghiaccio, Irene Motta, et al.
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of 14