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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.
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.
American Journal of Hematology|August 30, 2008
UGT1A1 promoter polymorphisms and the development of hyperbilirubinemia and gallbladder disease in children with sickle cell anemiaShannon L Carpenter, Susan Lieff, Thad A Howard, 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.
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.
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.
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.
Pharmacology|December 14, 2006
Effects of combined UDP-glucuronosyltransferase (UGT) 1A1*28 and 1A6*2 on paracetamol pharmacokinetics in beta-thalassemia/HbEJeeranut Tankanitlert, Noppawan Phumala Morales, Thad A Howard, et al.
African Journal of Laboratory Medicine|September 15, 2021
Operational analysis of the national sickle cell screening programme in the Republic of UgandaArielle G Hernandez, Charles Kiyaga, Thad A Howard, et al.
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