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Paediatric Drugs|August 31, 2017
State of the Art Management of Acute Vaso-occlusive Pain in Sickle Cell DiseaseLatika Puri, Kerri A Nottage, Jane S Hankins, et al.Journal of Pediatric Hematology/Oncology|July 17, 2015
Severe Autoimmune Hemolytic Anemia in an Infant Caused by Warm-reactive IGM and IGA Autoantibodies: A Case Report and Review of the LiteratureCristyn N Branstetter, Jane S Hankins, Dawn Moreau, et al.Plos One|March 4, 2015
Prevalence of vitamin D deficiency in sickle cell disease: a systematic reviewVikki G Nolan, Kerri A Nottage, Elliott W Cole, et al.British Journal of Haematology|January 29, 2014
Metabolic syndrome and cardiovascular risk among long-term survivors of acute lymphoblastic leukaemia - From the St. Jude Lifetime CohortKerri A Nottage, Kirsten K Ness, Chenghong Li, et al.Pediatric Blood & Cancer|September 6, 2018
Vaso-occlusive crisis as a predictor of symptomatic avascular necrosis in children with sickle cell diseaseAkram Mesleh Shayeb, Matthew P Smeltzer, Sue C Kaste, et al.Plos One|August 23, 2013
Hydroxyurea use and hospitalization trends in a comprehensive pediatric sickle cell programKerri A Nottage, Jane S Hankins, Matthew Smeltzer, et al.Pediatric Blood & Cancer|June 9, 2015
Paroxysmal cold hemoglobinuria due to an IgA Donath-Landsteiner antibodyNicholas S Whipple, Dawn A B Moreau, JoAnn M Moulds, et al.Hemoglobin|September 16, 2015
Distance from an Urban Sickle Cell Center and its Effects on Routine Healthcare Management and Rates of HospitalizationMatthew P Smeltzer, Vikki G Nolan, Xinhua Yu, et al.British Journal of Haematology|September 9, 2016
Hydroxycarbamide treatment and brain MRI/MRA findings in children with sickle cell anaemiaKerri A Nottage, Russell E Ware, Banu Aygun, et al.European Journal of Haematology|May 7, 2014
Predictors of splenic function preservation in children with sickle cell anemia treated with hydroxyureaKerri A Nottage, Russell E Ware, Bryan Winter, et al.Pageof 2