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Blood|April 5, 2013
A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD)Daniel H Wiseman, Alison May, Stephen Jolles, et al.
Haematologica|April 16, 2026
Immunosuppressive therapy for severe aplastic anemia in children under the age of 3 years yields a high response rate: a North American collaborative studyTalya Wittmann Dayagi, Laura Willis, Staci D Arnold, et al.
Haematologica|April 16, 2013
Sildenafil therapy in thalassemia patients with Doppler-defined risk of pulmonary hypertensionClaudia R Morris, Hae-Young Kim, John Wood, et al.
Blood|October 14, 2010
Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell diseaseMonica L Hulbert, Robert C McKinstry, JoAnne L Lacey, et al.
Pediatric Blood & Cancer|July 17, 2023
Return visit rates after an emergency department discharge for children with sickle cell pain episodesKeli D Coleman, Kenneth McKinley, Angela M Ellison, et al.
American Journal of Hematology|December 1, 2015
Effects of hydroxyurea treatment for patients with hemoglobin SC diseaseLori Luchtman-Jones, Sara Pressel, Lee Hilliard, et al.
Pediatric Blood & Cancer|May 3, 2025
Associations Between Pain Scores and Opioid Doses With Emergency Department Disposition and Return Visit Rates in Children With Sickle Cell DiseaseKeli D Coleman, Kenneth McKinley, Angela M Ellison, et al.
The New England Journal of Medicine|December 10, 2021
Betibeglogene Autotemcel Gene Therapy for Non-β0/β0 Genotype β-ThalassemiaFranco Locatelli, Alexis A Thompson, Janet L Kwiatkowski, et al.
JAMA Pediatrics|September 2, 2025
Opioid Timeliness in the Emergency Department and Hospitalizations for Acute Sickle Cell PainIbrahim Gwarzo, Keli D Coleman, Kenneth McKinley, et al.
Blood Advances|March 11, 2026
Newborn Screening Results for Sickle Cell Disease from the ASH Consortium on Newborn Screening in Africa (CONSA)Bernard Awuonda, Charles Kiyaga, Lulu Fred Chirande, et al.
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