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Clinical Chemistry|October 4, 2016
Stable-Isotope Dilution HPLC-Electrospray Ionization Tandem Mass Spectrometry Method for Quantifying Hydroxyurea in Dried Blood SamplesAnu Marahatta, Vandana Megaraj, Patrick T McGann, et al.
American Journal of Hematology|November 6, 2015
Characteristics of a rapid, point-of-care lateral flow immunoassay for the diagnosis of sickle cell diseasePatrick T McGann, Beverly A Schaefer, Mary Paniagua, et al.
Biomedicines|December 30, 2020
Electrochemical Determination of Hydroxyurea in a Complex Biological Matrix Using MoS<sub>2</sub>-Modified Electrodes and ChemometricsRemi Cazelles, Rajendra P Shukla, Russell E Ware, et al.
Blood|April 13, 2007
Hydroxyurea therapy lowers transcranial Doppler flow velocities in children with sickle cell anemiaSherri A Zimmerman, William H Schultz, Shelly Burgett, 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.
British Journal of Haematology|May 6, 2011
Chromosome damage and repair in children with sickle cell anaemia and long-term hydroxycarbamide exposurePatrick T McGann, Thad A Howard, Jonathan M Flanagan, et al.
Haematologica|April 10, 2010
Hydroxyurea therapy requires HbF induction for clinical benefit in a sickle cell mouse modelJeffrey D Lebensburger, Tamara I Pestina, Russell E Ware, et al.
The Journal of Pediatrics|March 16, 2020
Hydroxyurea Exposure in Lactation: a Pharmacokinetics Study (HELPS)Russell E Ware, Anu Marahatta, Julie L Ware, et al.
Experimental Hematology|January 30, 2007
Quantitative analysis of Howell-Jolly bodies in children with sickle cell diseaseVirginia L Harrod, Thad A Howard, Sherri A Zimmerman, et al.
Pediatric Hematology and Oncology|July 31, 2010
Severe thrombocytopenia with iron deficiency anemiaVan K Morris, Holly L Spraker, Scott C Howard, et al.
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