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Haematologica|March 17, 2018
Proteomic analysis of plasma from children with sickle cell anemia and silent cerebral infarctionSanjay Tewari, George Renney, John Brewin, et al.Haematologica|December 23, 2020
Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC)John N Brewin, Helen Rooks, Kate Gardner, et al.Blood Advances|March 10, 2022
Genetic variants of PKLR are associated with acute pain in sickle cell diseaseXunde Wang, Kate Gardner, Mickias B Tegegn, et al.Plos One|July 26, 2017
The significance of inadequate transcranial Doppler studies in children with sickle cell diseaseSimon Greenwood, Colin Deane, Oliver L Rees, et al.The Lancet. Haematology|May 1, 2019
Effect of low-level BCR-ABL1 kinase domain mutations identified by next-generation sequencing in patients with chronic myeloid leukaemia: a population-based studyAytug Kizilors, Elena Crisà, Nicholas Lea, et al.Studies in Health Technology and Informatics|October 4, 2007
Empowering patients to improve the quality of their care: design and implementation of a shared health maintenance module in a US integrated healthcare delivery networkEric G Poon, Jonathan Wald, Jeffrey L Schnipper, et al.AMIA ... Annual Symposium Proceedings. AMIA Symposium|November 13, 2008
Effectiveness of health maintenance reminders provided directly to patientsAdam Wright, Eric G Poon, Jonathan Wald, et al.Journal of General Internal Medicine|September 10, 2011
Randomized controlled trial of health maintenance reminders provided directly to patients through an electronic PHRAdam Wright, Eric G Poon, Jonathan Wald, et al.Blood Advances|February 14, 2018
g(HbF): a genetic model of fetal hemoglobin in sickle cell diseaseKate Gardner, Tony Fulford, Nicholas Silver, et al.American Journal of Hematology|August 23, 2018
Prognostic factors of disease severity in infants with sickle cell anemia: A comprehensive longitudinal cohort studyValentine Brousse, Sara El Hoss, Naïm Bouazza, et al.Pageof 4