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Journal of Pediatric Psychology|April 5, 2022
Adaptive Functioning in Children and Adolescents With Sickle Cell DiseaseAna Trpchevska, Jennifer Longoria, Victoria Okhomina, et al.Journal of Pediatric Hematology/Oncology|November 25, 2020
Use of Wise Device Technology to Measure Adherence to Hydroxyurea Therapy in Youth With Sickle Cell DiseaseLisa M Ingerski, Megan Loew, Jerlym S Porter, et al.Medicine|December 20, 2014
From infancy to adolescence: fifteen years of continuous treatment with hydroxyurea in sickle cell anemiaJane S Hankins, Banu Aygun, Kerri Nottage, et al.Journal of Pediatric Hematology/Oncology|August 5, 2014
Genetic education and sickle cell disease: feasibility and efficacy of a program tailored to adolescentsJerlym S Porter, Christy S Matthews, Yvonne M Carroll, 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 8, 2007
Preservation of spleen and brain function in children with sickle cell anemia treated with hydroxyureaJane S Hankins, Kathleen J Helton, M Beth McCarville, et al.Pediatric Radiology|June 20, 2012
The impact of preparation and support procedures for children with sickle cell disease undergoing MRIKatherine R Cejda, Matthew P Smeltzer, Eileen N Hansbury, et al.Journal of Pediatric Health Care : Official Publication of National Association of Pediatric Nurse Associates & Practitioners|July 24, 2012
A transition pilot program for adolescents with sickle cell diseaseJane S Hankins, Raymond Osarogiagbon, Patricia Adams-Graves, et al.The Clinical Journal of Pain|October 23, 2020
Pain in Youth With Sickle Cell Disease: A Report From the Sickle Cell Clinical Research and Intervention ProgramNicole M Alberts, Guolian Kang, Chen Li, et al.Annals of Hematology|July 14, 2023
Age-related differences in risks and outcomes of 30-day readmission in adults with sickle cell diseaseMing Chen, Kenneth I Ataga, Jane S Hankins, et al.Pageof 21