Opoka, RO; Ndugwa, CM; Latham, TS; Lane, A; Hume, HA; Kasirye, P; Hodges, JS; Ware, RE; John, CC.
Novel use Of Hydroxyurea in an African Region with Malaria (NOHARM): a trial for children with sickle cell anemia.
Blood.
2017;
130:2585-2593.
Ambrose, EE; Smart, LR; Hokororo, A; Charles, M; Beyanga, M; Hernandez, AG; Howard, TA; Ware, RE.
Prevalence and mapping of sickle cell disease in northwestern Tanzania.
Blood Advances.
2017;
1:26-28.
Estepp, JH; Smeltzer, MP; Kang, G; Li, C; Wang, WC; Abrams, C; Aygun, B; Ware, RE; Nottage, K; Hankins, JS.
A clinically meaningful fetal hemoglobin threshold for children with sickle cell anemia during hydroxyurea therapy.
American Journal of Hematology.
2017;
92:1333-1339.
Alvarez, O; Nottage, K; Simpson, LM; Wood, J; Davis, BR; Fuh, B; Sarnaik, S; Aygun, B; Helton, K; Ware, RE.
Kidney function of transfused children with sickle cell anemia: Baseline data from the TWiTCH study with comparison to non-transfused cohorts.
American Journal of Hematology.
2017;
92:E637-E639.
Marahatta, A; Ware, RE.
Hydroxyurea: Analytical techniques and quantitative analysis.
Blood Cells, Molecules, and Diseases.
2017;
67:135-142.
Ware, RE.
Technological Advances in Sickle Cell Disease.
Blood Cells, Molecules, and Diseases.
2017;
67:102-103.
Chou, ST; Flanagan, JM; Vege, S; Luban, NL C; Brown, RC; Ware, RE; Westhoff, CM.
Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemia.
Blood Advances.
2017;
1:1414-1422.
Rotz, SJ; Palumbo, JS; Ware, RE.
Type 2B von Willebrand Disease: An Unusual Cause of Severe Neonatal Thrombocytopenia.
Journal of Pediatric Hematology/Oncology.
2017;
39:473-475.
Ware, RE; de Montalembert, M; Tshilolo, L; Abboud, MR.
Sickle cell disease.
The Lancet.
2017;
390:311-323.
Jeste, ND; Sanchez, LM; Urcuyo, GS; Berges, ME; Luden, JP; Stuber, SE; Latham, TS; Mena, R; Nieves, RM; Ware, RE.
Stroke Avoidance for Children in REpublica Dominicana (SACRED): Protocol for a Prospective Study of Stroke Risk and Hydroxyurea Treatment in Sickle Cell Anemia.
JMIR Research Protocols.
2017;
6:e107-e107.
McGann, PT; Hernandez, AG; Ware, RE.
Sickle cell anemia in sub-Saharan Africa: advancing the clinical paradigm through partnerships and research.
Blood.
2017;
129:155-161.
Crosby, LE; Ware, RE; Goldstein, A; Walton, A; Joffe, NE; Vogel, C; Britto, MT.
Development and evaluation of iManage: A self-management app co-designed by adolescents with sickle cell disease.
Pediatric Blood and Cancer.
2017;
64:139-145.
Crosby, LE; Joffe, NE; Peugh, J; Ware, RE; Britto, MT.
Pilot of the Chronic Disease Self-Management Program for Adolescents and Young Adults With Sickle Cell Disease.
Journal of Adolescent Health.
2017;
60:120-123.
Niss, O; Ware, RE.
Sickle Cell Disease.
In: Ekvall SW; Ekvall VK, Ed.
Pediatric and Adult Nutrition in Chronic Diseases, Developmental Disabilities, and Hereditary Metabolic Disorders: Prevention, Assessment, and Treatment.
New York:
Oxford University Press;
2017.
McGann, PT; Nero, AC; Ware, RE.
Clinical features of β-thalassemia and sickle cell disease.
Advances in Experimental Medicine and Biology.
2017;
1013:1-26.