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Journal of Sickle Cell Disease
|
June 17, 2025
Recommended measurement protocols for sickle cell disease in the PhenX toolkit: psychosocial factors and social determinants of health
Lori E Crosby, Desireé N Williford, Allison A King, et al.
Orphanet Journal of Rare Diseases
|
July 9, 2020
Publication of data collection forms from NHLBI funded sickle cell disease implementation consortium (SCDIC) registry
Jeffrey A Glassberg, Elizabeth A Linton, Katrina Burson, et al.
JAMA Network Open
|
January 17, 2025
Brain Age Modeling and Cognitive Outcomes in Young Adults With and Without Sickle Cell Anemia
Andria L Ford, Slim Fellah, Yan Wang, et al.
American Journal of Hematology
|
October 15, 2013
Parent education and biologic factors influence on cognition in sickle cell anemia
Allison A King, John J Strouse, Mark J Rodeghier, et al.
JMIR Research Protocols
|
June 14, 2022
Primary Prevention of Stroke in Children With Sickle Cell Anemia in Nigeria: Protocol for a Mixed Methods Implementation Study in a Community Hospital
Halima Bello-Manga, Lawal Haliru, Kudrat Abdulkareem Ahmed, et al.
Plos One
|
October 29, 2021
Sex-based differences in the manifestations and complications of sickle cell disease: Report from the Sickle Cell Disease Implementation Consortium
Rita V Masese, Dominique Bulgin, Mitchell R Knisely, et al.
British Journal of Haematology
|
February 11, 2021
Cognitive performance as a predictor of healthcare transition in sickle cell disease
Anjelica C Saulsberry-Abate, Marita Partanen, Jerlym S Porter, et al.
Current Research in Translational Medicine
|
January 20, 2024
Catechol-O-methyltransferase gene (COMT) is associated with neurocognitive functioning in patients with sickle cell disease
Andrew M Heitzer, Sara R Rashkin, Ana Trpchevska, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
|
January 10, 2017
Current Results and Future Research Priorities in Late Effects after Hematopoietic Stem Cell Transplantation for Children with Sickle Cell Disease and Thalassemia: A Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects after Pediatric Hematopoietic Stem Cell Transplantation
Shalini Shenoy, Emanuele Angelucci, Staci D Arnold, et al.
Pediatric Blood & Cancer
|
May 6, 2025
User Perceptions of a Multilevel mHealth Intervention to Boost Adherence to Hydroxyurea in Sickle Cell Disease
Christina M Abrams, Natalia Davila, Sherif M Badawy, et al.
Page
of 15
Search research articles
Search
Showing results (101-110 of 147) with videos related to
Sort By:
Page
of 15
Journal of Sickle Cell Disease
|
June 17, 2025
Recommended measurement protocols for sickle cell disease in the PhenX toolkit: psychosocial factors and social determinants of health
Lori E Crosby, Desireé N Williford, Allison A King, et al.
Orphanet Journal of Rare Diseases
|
July 9, 2020
Publication of data collection forms from NHLBI funded sickle cell disease implementation consortium (SCDIC) registry
Jeffrey A Glassberg, Elizabeth A Linton, Katrina Burson, et al.
JAMA Network Open
|
January 17, 2025
Brain Age Modeling and Cognitive Outcomes in Young Adults With and Without Sickle Cell Anemia
Andria L Ford, Slim Fellah, Yan Wang, et al.
American Journal of Hematology
|
October 15, 2013
Parent education and biologic factors influence on cognition in sickle cell anemia
Allison A King, John J Strouse, Mark J Rodeghier, et al.
JMIR Research Protocols
|
June 14, 2022
Primary Prevention of Stroke in Children With Sickle Cell Anemia in Nigeria: Protocol for a Mixed Methods Implementation Study in a Community Hospital
Halima Bello-Manga, Lawal Haliru, Kudrat Abdulkareem Ahmed, et al.
Plos One
|
October 29, 2021
Sex-based differences in the manifestations and complications of sickle cell disease: Report from the Sickle Cell Disease Implementation Consortium
Rita V Masese, Dominique Bulgin, Mitchell R Knisely, et al.
British Journal of Haematology
|
February 11, 2021
Cognitive performance as a predictor of healthcare transition in sickle cell disease
Anjelica C Saulsberry-Abate, Marita Partanen, Jerlym S Porter, et al.
Current Research in Translational Medicine
|
January 20, 2024
Catechol-O-methyltransferase gene (COMT) is associated with neurocognitive functioning in patients with sickle cell disease
Andrew M Heitzer, Sara R Rashkin, Ana Trpchevska, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
|
January 10, 2017
Current Results and Future Research Priorities in Late Effects after Hematopoietic Stem Cell Transplantation for Children with Sickle Cell Disease and Thalassemia: A Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects after Pediatric Hematopoietic Stem Cell Transplantation
Shalini Shenoy, Emanuele Angelucci, Staci D Arnold, et al.
Pediatric Blood & Cancer
|
May 6, 2025
User Perceptions of a Multilevel mHealth Intervention to Boost Adherence to Hydroxyurea in Sickle Cell Disease
Christina M Abrams, Natalia Davila, Sherif M Badawy, et al.
Page
of 15