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British Journal of Haematology|August 20, 2013
Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemiaChristopher J Bean, Sheree L Boulet, Genyan Yang, et al.
Clinical Trials (London, England)|November 15, 2018
Developing a risk-based composite neurologic outcome for a trial of hydroxyurea in young children with sickle cell diseaseJames F Casella, Robert J Adams, Donald J Brambilla, et al.
American Journal of Hematology|October 15, 2013
Parent education and biologic factors influence on cognition in sickle cell anemiaAllison A King, John J Strouse, Mark J Rodeghier, et al.
Pediatric Blood & Cancer|October 9, 2009
Transcranial doppler ultrasonography (TCD) in infants with sickle cell anemia: baseline data from the BABY HUG trialSteven G Pavlakis, Renée C Rees, Xiangke Huang, et al.
Pediatrics|July 4, 2006
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylationRonald D Cohn, Erik Eklund, Amanda L Bergner, et al.
The Journal of Pediatrics|November 3, 2009
Renal function in infants with sickle cell anemia: baseline data from the BABY HUG trialRussell E Ware, Renee C Rees, Sharada A Sarnaik, et al.
Journal of Pediatric Intensive Care|August 11, 2023
Perioperative Management of Pediatric Patients with Moyamoya ArteriopathySarah E Gardner Yelton, Monica A Williams, Mollie Young, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 22, 2018
Diagnostic utility of telomere length testing in a hospital-based settingJonathan K Alder, Vidya Sagar Hanumanthu, Margaret A Strong, et al.
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