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Pediatric Blood & Cancer|August 27, 2025
HABIT Efficacy Trial Intervention Improves Elements of General and Disease-Specific Quality of Life in Youth With Sickle Cell DiseaseArlene Smaldone, Deepa Manwani, Banu Aygun, et al.Journal of Pediatric Psychology|March 23, 2002
Neurocognitive development of young children with sickle cell disease through three years of ageRobert J Thompson, Kathryn E Gustafson, Melanie J Bonner, et al.Pediatric Blood & Cancer|July 8, 2024
Assessing multilevel barriers to hydroxyurea adherence in youth with sickle cell disease using pharmacy-based refill recordsArlene Smaldone, Deepa Manwani, Banu Aygun, et al.The Journal of Laboratory and Clinical Medicine|April 5, 2003
UGT1A promoter polymorphisms influence bilirubin response to hydroxyurea therapy in sickle cell anemiaMatthew M Heeney, Thad A Howard, Sherri A Zimmerman, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 3, 2007
Short stature in children with sickle cell anemia correlates with alterations in the IGF-I axisPaulo F Collett-Solberg, Don Fleenor, William H Schultz, et al.Pediatric Dermatology|September 30, 2005
Successful treatment of refractory childhood pemphgus vulgaris with anti-CD20 monoclonal antibody (rituximab)Heidi H Kong, Neil S Prose, Russell E Ware, et al.American Journal of Hematology|November 29, 2011
A novel laboratory technique demonstrating the influences of RHD zygosity and the RhCcEe phenotype on erythrocyte D antigen expressionPatrick T McGann, Jenny M Despotovic, Thad A Howard, et al.Pediatric Blood & Cancer|October 14, 2014
Shared decision making for hydroxyurea treatment initiation in children with sickle cell anemiaLori E Crosby, Lisa M Shook, Russell E Ware, et al.American Journal of Hematology|September 29, 2015
Prevention of conversion to abnormal transcranial Doppler with hydroxyurea in sickle cell anemia: A Phase III international randomized clinical trialJane S Hankins, Mary Beth McCarville, Angela Rankine-Mullings, et al.Pediatric Blood & Cancer|April 30, 2013
Transcranial Doppler velocity and brain MRI/MRA changes in children with sickle cell anemia on chronic transfusions to prevent primary strokeVivien A Sheehan, Eileen N Hansbury, Matthew P Smeltzer, et al.Pageof 27