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Russell E Ware

Showing results (201-210 of 267) with videos related to

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Blood|March 7, 2009
R2* magnetic resonance imaging of the liver in patients with iron overloadJane S Hankins, M Beth McCarville, Ralf B Loeffler, et al.
British Journal of Haematology|March 6, 2018
Transcranial Doppler velocity among Jamaican children with sickle cell anaemia: determining the significance of haematological values and nutritionAngela E Rankine-Mullings, Nadine Morrison-Levy, Deanne Soares, et al.
Pediatric Blood & Cancer|August 15, 2015
Hydroxyurea Therapy for Children With Sickle Cell Anemia in Sub-Saharan Africa: Rationale and Design of the REACH TrialPatrick T McGann, Léon Tshilolo, Brigida Santos, et al.
International Journal of Public Health|August 2, 2021
Prospective Newborn Screening for Sickle Cell Disease and Other Inherited Blood Disorders in Central MalawiGerald Tegha, Hillary M Topazian, Portia Kamthunzi, et al.
American Journal of Hematology|May 21, 2019
Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemiaPatrick T McGann, Omar Niss, Min Dong, et al.
British Journal of Haematology|April 7, 2009
Chronic transfusion practice for children with sickle cell anaemia and strokeBanu Aygun, Marsha A McMurray, William H Schultz, et al.
The Journal of Pediatrics|September 13, 2011
Effects of chronic transfusions on abdominal sonographic abnormalities in children with sickle cell anemiaMary Beth McCarville, Zora R Rogers, Sharada Sarnaik, et al.
British Journal of Haematology|November 3, 2015
Organ iron accumulation in chronically transfused children with sickle cell anaemia: baseline results from the TWiTCH trialJohn C Wood, Alan R Cohen, Sara L Pressel, et al.
Blood|January 5, 2002
Predictors of fetal hemoglobin response in children with sickle cell anemia receiving hydroxyurea therapyRussell E Ware, Barry Eggleston, Rupa Redding-Lallinger, et al.
Bulletin of the World Health Organization|December 9, 2020
Surveillance for sickle cell disease, United Republic of TanzaniaEmmanuela E Ambrose, Luke R Smart, Mwesige Charles, et al.
Pageof 27

Showing results (201-210 of 267) with videos related to

Sort By:
Pageof 27
Blood|March 7, 2009
R2* magnetic resonance imaging of the liver in patients with iron overloadJane S Hankins, M Beth McCarville, Ralf B Loeffler, et al.
British Journal of Haematology|March 6, 2018
Transcranial Doppler velocity among Jamaican children with sickle cell anaemia: determining the significance of haematological values and nutritionAngela E Rankine-Mullings, Nadine Morrison-Levy, Deanne Soares, et al.
Pediatric Blood & Cancer|August 15, 2015
Hydroxyurea Therapy for Children With Sickle Cell Anemia in Sub-Saharan Africa: Rationale and Design of the REACH TrialPatrick T McGann, Léon Tshilolo, Brigida Santos, et al.
International Journal of Public Health|August 2, 2021
Prospective Newborn Screening for Sickle Cell Disease and Other Inherited Blood Disorders in Central MalawiGerald Tegha, Hillary M Topazian, Portia Kamthunzi, et al.
American Journal of Hematology|May 21, 2019
Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemiaPatrick T McGann, Omar Niss, Min Dong, et al.
British Journal of Haematology|April 7, 2009
Chronic transfusion practice for children with sickle cell anaemia and strokeBanu Aygun, Marsha A McMurray, William H Schultz, et al.
The Journal of Pediatrics|September 13, 2011
Effects of chronic transfusions on abdominal sonographic abnormalities in children with sickle cell anemiaMary Beth McCarville, Zora R Rogers, Sharada Sarnaik, et al.
British Journal of Haematology|November 3, 2015
Organ iron accumulation in chronically transfused children with sickle cell anaemia: baseline results from the TWiTCH trialJohn C Wood, Alan R Cohen, Sara L Pressel, et al.
Blood|January 5, 2002
Predictors of fetal hemoglobin response in children with sickle cell anemia receiving hydroxyurea therapyRussell E Ware, Barry Eggleston, Rupa Redding-Lallinger, et al.
Bulletin of the World Health Organization|December 9, 2020
Surveillance for sickle cell disease, United Republic of TanzaniaEmmanuela E Ambrose, Luke R Smart, Mwesige Charles, et al.
Pageof 27