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Pediatric Hematology and Oncology|June 24, 2008
Chemical and functional analysis of generic hydroxyurea formulationsVirginia L Harrod, Thad Howard, Miguel R Abboud, et al.Pediatric Blood & Cancer|August 24, 2010
The diagnostic dilemma of congenital unstable hemoglobinopathiesAmber M Yates, Nicole A Mortier, Kristina S Hyde, et al.Journal of Pediatric Hematology/Oncology|May 6, 2004
Chemical and functional analysis of hydroxyurea oral solutionsMatthew M Heeney, Matthew R Whorton, Thad A Howard, et al.Pediatric Blood & Cancer|July 12, 2005
Pelger-Huët anomaly in a child with 1q42.3-44 deletionTheodosia A Kalfa, Sherri A Zimmerman, Barbara K Goodman, et al.Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|June 10, 2018
Concomitant endometriosis in malignant and borderline ovarian tumours<sup></sup>Engin Oral, Ovgu Aydin, Banu Aygun Kumbak, et al.Journal of Pediatric Hematology/Oncology|September 29, 2012
Phenocopy of warfarin syndrome in an infant born to a mother with sickle cell anemia and severe transfusional iron overloadYi Xie, Eniko K Pivnick, Harris L Cohen, et al.Analytical Chemistry|October 8, 2025
Microsensor Array for the Electrochemical Analysis of Hydroxyurea in Blood Samples of Children Affected by Sickle Cell AnemiaRajendra P Shukla, Matan Aroosh, Remi Cazelles, 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|May 30, 2006
Beta-thalassemia intermedia due to compound heterozygosity for two beta-globin gene promoter mutations, including a novel TATA box deletionRaveen K Basran, Ulrike M Reiss, Hong-Yuan Luo, 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.Pageof 27