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Pediatric Blood & Cancer|May 2, 2013
Acute care of pediatric patients with sickle cell disease: a simulation performance assessmentTracy L Burns, Michael R DeBaun, John R Boulet, et al.American Journal of Obstetrics and Gynecology|March 10, 2007
Risk for postterm delivery after previous postterm deliveryZachary A-F Kistka, Lisanne Palomar, Sarah E Boslaugh, et al.Blood Advances|November 16, 2022
Underweight children older than 5 years with sickle cell anemia are at risk for early mortality in a low-resource settingLauren J Klein, Shehu Umar Abdullahi, Safiya Gambo, et al.The Journal of Allergy and Clinical Immunology|March 11, 2011
Elevation of IgE in children with sickle cell disease is associated with doctor diagnosis of asthma and increased morbidityPing An, Emily A Barron-Casella, Robert C Strunk, et al.Pediatric Blood & Cancer|February 19, 2013
Exploring barriers and facilitators to clinical trial enrollment in the context of sickle cell anemia and hydroxyureaJeffrey D Lebensburger, Robert F Sidonio, Michael R Debaun, et al.American Journal of Human Genetics|January 29, 2002
Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defectsMichael R DeBaun, Emily L Niemitz, D Elizabeth McNeil, et al.Blood Advances|September 27, 2023
Risk factors in underweight older children with sickle cell anemia: a comparison of low- to high-income countriesLauren Jane Klein, Shehu Umar Abdullahi, Safiya Gambo, et al.Pediatric Blood & Cancer|February 6, 2010
Variability of pulse oximetry measurement over 1 year in children with sickle cell disease depends on initial oxygen saturation measurementJonathan E Mullin, Ben Cooper, Sinziana Seicean, et al.The Journal of Molecular Diagnostics : JMD|July 10, 2010
Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yieldJochen K Lennerz, Robert J Timmerman, Dorothy K Grange, et al.Pediatric Blood & Cancer|April 23, 2014
Randomization is not associated with socio-economic and demographic factors in a multi-center clinical trial of children with sickle cell anemiaDionna O Roberts, Brittany Covert, Mark J Rodeghier, et al.Pageof 27