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Journal of Clinical Medicine|November 8, 2019
GSTM1 and Liver Iron Content in Children with Sickle Cell Anemia and Iron OverloadLatika Puri, Jonathan M Flanagan, Guolian Kang, et al.
The Pharmacogenomics Journal|September 13, 2018
Concordance between glucose-6-phosphate dehydrogenase (G6PD) genotype and phenotype and rasburicase use in patients with hematologic malignanciesKatherine M Robinson, Wenjian Yang, Cyrine E Haidar, et al.
Annals of Emergency Medicine|September 15, 2020
A Survey-Based Needs Assessment of Barriers to Optimal Sickle Cell Disease Care in the Emergency DepartmentElizabeth A Linton, Dania A Goodin, Jane S Hankins, et al.
American Journal of Hematology|August 5, 2021
Patient-reported neurocognitive symptoms influence instrumental activities of daily living in sickle cell diseaseJennifer N Longoria, Norma L Pugh, Victor Gordeuk, et al.
Blood Advances|June 13, 2022
Longitudinal study of glomerular hyperfiltration in adults with sickle cell anemia: a multicenter pooled analysisKenneth I Ataga, Qingning Zhou, Santosh L Saraf, et al.
American Journal of Hematology|March 7, 2024
Mortality in adults with sickle cell disease: Results from the sickle cell disease implementation consortium (SCDIC) registryFranklin Njoku, Norma Pugh, Donald Brambilla, et al.
JAMA Network Open|May 18, 2023
Examining Mental Health, Education, Employment, and Pain in Sickle Cell DiseaseKelly M Harris, Liliana Preiss, Taniya Varughese, et al.
Pediatric Blood & Cancer|July 20, 2024
Perinatal risk factors and neurocognitive outcomes in children and adolescents with sickle cell diseaseJennifer N Longoria, Christina M Dandar, Joshua H Semko, et al.
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