Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Deepa Manwani

Showing results (121-130 of 138) with videos related to

Pageof 14
Sort By:
Clinicoeconomics and Outcomes Research : CEOR|November 5, 2020
Development of a Severity Classification System for Sickle Cell DiseaseNirmish 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 RegistryMartha 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 activationChengjie 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 syndromeKerry 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 patientsLaura 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 registrySamuel 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 anaemiasFrancesca 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 ResearchAndrew 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 StatementSeethal 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 rebalanceAlisa Dong, Valentina Ghiaccio, Irene Motta, et al.
Pageof 14

Showing results (121-130 of 138) with videos related to

Sort By:
Pageof 14
Clinicoeconomics and Outcomes Research : CEOR|November 5, 2020
Development of a Severity Classification System for Sickle Cell DiseaseNirmish 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 RegistryMartha 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 activationChengjie 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 syndromeKerry 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 patientsLaura 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 registrySamuel 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 anaemiasFrancesca 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 ResearchAndrew 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 StatementSeethal 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 rebalanceAlisa Dong, Valentina Ghiaccio, Irene Motta, et al.
Pageof 14