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Russell E Ware

Showing results (101-110 of 267) with videos related to

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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|February 18, 2011
Hydroxyurea adherence and associated outcomes among Medicaid enrollees with sickle cell diseaseSean D Candrilli, Sarah H O'Brien, Russell E Ware, 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.
American Journal of Hematology|August 29, 2015
An accurate and inexpensive color-based assay for detecting severe anemia in a limited-resource settingPatrick T McGann, Erika A Tyburski, Vysolela de Oliveira, et al.
Blood Advances|March 24, 2024
Successes and pitfalls in orphan drug development for sickle cell diseaseEnrico Costa, Antonella Isgrò, Mariane de Montalembert, et al.
Blood|February 23, 2012
Silent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemiaMichael R DeBaun, F Daniel Armstrong, Robert C McKinstry, et al.
Blood|June 15, 1994
Chromosomal assignment of genes involved in glycosylphosphatidylinositol anchor biosynthesis: implications for the pathogenesis of paroxysmal nocturnal hemoglobinuriaRussell E Ware, Thad A Howard, Tetsu Kamitani, et al.
American Journal of Hematology|December 21, 2012
Hydroxyurea treatment decreases glomerular hyperfiltration in children with sickle cell anemiaBanu Aygun, Nicole A Mortier, Matthew P Smeltzer, et al.
Pediatric Blood & Cancer|June 8, 2007
Preservation of spleen and brain function in children with sickle cell anemia treated with hydroxyureaJane S Hankins, Kathleen J Helton, M Beth McCarville, 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.
Pageof 27

Showing results (101-110 of 267) with videos related to

Sort By:
Pageof 27
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|February 18, 2011
Hydroxyurea adherence and associated outcomes among Medicaid enrollees with sickle cell diseaseSean D Candrilli, Sarah H O'Brien, Russell E Ware, 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.
American Journal of Hematology|August 29, 2015
An accurate and inexpensive color-based assay for detecting severe anemia in a limited-resource settingPatrick T McGann, Erika A Tyburski, Vysolela de Oliveira, et al.
Blood Advances|March 24, 2024
Successes and pitfalls in orphan drug development for sickle cell diseaseEnrico Costa, Antonella Isgrò, Mariane de Montalembert, et al.
Blood|February 23, 2012
Silent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemiaMichael R DeBaun, F Daniel Armstrong, Robert C McKinstry, et al.
Blood|June 15, 1994
Chromosomal assignment of genes involved in glycosylphosphatidylinositol anchor biosynthesis: implications for the pathogenesis of paroxysmal nocturnal hemoglobinuriaRussell E Ware, Thad A Howard, Tetsu Kamitani, et al.
American Journal of Hematology|December 21, 2012
Hydroxyurea treatment decreases glomerular hyperfiltration in children with sickle cell anemiaBanu Aygun, Nicole A Mortier, Matthew P Smeltzer, et al.
Pediatric Blood & Cancer|June 8, 2007
Preservation of spleen and brain function in children with sickle cell anemia treated with hydroxyureaJane S Hankins, Kathleen J Helton, M Beth McCarville, 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.
Pageof 27