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Journal of Pediatric Hematology/Oncology|September 29, 2012
Phenocopy of warfarin syndrome in an infant born to a mother with sickle cell anemia and severe transfusional iron overloadYi Xie, Eniko K Pivnick, Harris L Cohen, et al.Pediatric Blood & Cancer|April 29, 2017
The clinical severity of hemoglobin S/Black (<sup>A</sup> γδβ)<sup>0</sup> -thalassemiaMaria I Cancio, Banu Aygun, David H K Chui, et al.Pediatric Blood & Cancer|February 8, 2011
Neurocognitive screening with the Brigance preschool screen-II in 3-year-old children with sickle cell diseaseBanu Aygun, Jennifer Parker, Molly B Freeman, et al.BMC Pediatrics|October 17, 2019
HABIT efficacy and sustainability trial, a multi-center randomized controlled trial to improve hydroxyurea adherence in youth with sickle cell disease: a study protocolArlene Smaldone, Deepa Manwani, Banu Aygun, et al.British Journal of Haematology|October 25, 2011
Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobinDuyen A Ngo, Banu Aygun, Idowu Akinsheye, et al.Pediatric Blood & Cancer|February 6, 2024
Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment (HABIT) efficacy trial: Community health worker support may increase hydroxyurea adherence of youth with sickle cell diseaseNancy S Green, Deepa Manwani, Banu Aygun, et al.Pediatric Pulmonology|November 5, 2020
NT-proBNP levels and cardiopulmonary function in children with sickle cell diseaseLance Feld, Elizabeth K Fiorino, Banu Aygun, et al.British Journal of Haematology|September 9, 2016
Hydroxycarbamide treatment and brain MRI/MRA findings in children with sickle cell anaemiaKerri A Nottage, Russell E Ware, Banu Aygun, et al.European Journal of Haematology|May 7, 2014
Predictors of splenic function preservation in children with sickle cell anemia treated with hydroxyureaKerri A Nottage, Russell E Ware, Bryan Winter, et al.British Journal of Haematology|August 16, 2021
Developmental screening of three-year-old children with sickle cell disease compared to controlsWinfred Wang, Molly Freeman, Latacha Hamilton, et al.Pageof 8