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Russell E Ware

Showing results (91-100 of 267) with videos related to

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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.
Pediatric Hematology and Oncology|June 24, 2008
Chemical and functional analysis of generic hydroxyurea formulationsVirginia L Harrod, Thad Howard, Miguel R Abboud, et al.
Haematologica|November 26, 2016
Different clinical characteristics of paroxysmal nocturnal hemoglobinuria in pediatric and adult patientsÁlvaro Urbano-Ispizua, Petra Muus, Hubert Schrezenmeier, 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.
Blood|December 7, 2007
Defective binding of factor XI-N248 to activated human plateletsMao-Fu Sun, David Ho, Danko Martincic, 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.
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.
Pageof 27

Showing results (91-100 of 267) with videos related to

Sort By:
Pageof 27
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.
Pediatric Hematology and Oncology|June 24, 2008
Chemical and functional analysis of generic hydroxyurea formulationsVirginia L Harrod, Thad Howard, Miguel R Abboud, et al.
Haematologica|November 26, 2016
Different clinical characteristics of paroxysmal nocturnal hemoglobinuria in pediatric and adult patientsÁlvaro Urbano-Ispizua, Petra Muus, Hubert Schrezenmeier, 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.
Blood|December 7, 2007
Defective binding of factor XI-N248 to activated human plateletsMao-Fu Sun, David Ho, Danko Martincic, 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.
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.
Pageof 27