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Pediatric Blood & Cancer|August 24, 2010
The diagnostic dilemma of congenital unstable hemoglobinopathiesAmber M Yates, Nicole A Mortier, Kristina S Hyde, et al.Pediatric Blood & Cancer|February 6, 2013
Effects of adenotonsillectomy on polysomnographic parameters in children with sickle cell diseasePaul Finch, Rose Mary Stocks, Matthew P Smeltzer, et al.Journal of Pediatric Psychology|June 23, 2017
Pediatric to Adult Care Transition: Perspectives of Young Adults With Sickle Cell DiseaseJerlym S Porter, Kimberly M Wesley, Mimi S Zhao, et al.Leukemia & Lymphoma|November 21, 2012
Trends in transfusion burden among long-term survivors of childhood hematological malignanciesKerri Nottage, James G Gurney, Matthew Smeltzer, 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.American Journal of Hematology|April 23, 2009
Microarray analysis of liver gene expression in iron overloaded patients with sickle cell anemia and beta-thalassemiaJonathan M Flanagan, Shirley Steward, Jane S Hankins, et al.Pediatric Blood & Cancer|August 19, 2014
Improved hydroxyurea effect with the use of text messaging in children with sickle cell anemiaJeremie H Estepp, Bryan Winter, Margery Johnson, et al.Pediatric Blood & Cancer|May 10, 2020
Measuring hydroxyurea adherence by pharmacy and laboratory data compared with video observation in children with sickle cell diseaseSusan Creary, Deena Chisolm, Joseph Stanek, et al.Hemoglobin|June 19, 2014
Assessment of sleep-related disorders in children with sickle cell diseaseJane S Hankins, Nina I Verevkina, Matthew P Smeltzer, et al.Intellectual and Developmental Disabilities|August 21, 2010
"It's our job": qualitative study of family responses to ableismSusan L Neely-Barnes, J Carolyn Graff, Ruth J Roberts, et al.Pageof 21