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Pediatric Blood & Cancer|November 11, 2025
Taking Care of the Caregivers: A Quality-of-Life Measure for the Parents of Children With Transfusion-DependentRobert J Klaassen, Rania S Khelifi, Nicholas Barrowman, et al.
European Journal of Haematology|December 17, 2013
Cost-effectiveness analysis of preoperative transfusion in patients with sickle cell disease using evidence from the TAPS trialEldon Spackman, Mark Sculpher, Jo Howard, et al.
British Journal of Haematology|May 22, 2020
Genotype-phenotype correlation in children with hereditary spherocytosisSoumitra Tole, Priya Dhir, Jakob Pugi, et al.
Journal of Clinical and Translational Science|February 6, 2025
A pilot randomized controlled trial of the iPeer2Peer program in adolescents with sickle cell disease: A mixed method studyLauren Kelenc, Brittany Wiles, Fareha Nishat, et al.
JMIR Pediatrics and Parenting|September 14, 2019
Exploring the Needs of Adolescents With Sickle Cell Disease to Inform a Digital Self-Management and Transitional Care Program: Qualitative StudyYalinie Kulandaivelu, Chitra Lalloo, Richard Ward, et al.
Lancet (London, England)|January 29, 2013
The Transfusion Alternatives Preoperatively in Sickle Cell Disease (TAPS) study: a randomised, controlled, multicentre clinical trialJo Howard, Moira Malfroy, Charlotte Llewelyn, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|July 4, 2020
Outcomes of haemoglobin Bart's hydrops fetalis following intrauterine transfusion in Ontario, CanadaHui Jue Zhang, Ali Amid, Laura A Janzen, et al.
British Journal of Haematology|November 5, 2013
Validation and reliability of a disease-specific quality of life measure (the TranQol) in adults and children with thalassaemia majorRobert J Klaassen, Nicholas Barrowman, Manuela Merelles-Pulcini, et al.
Healthcare Quarterly (Toronto, Ont.)|April 25, 2022
Ensuring Equity and Inclusion in Virtual Care Best Practices for Diverse Populations of Youth with Chronic PainKathryn A Birnie, Tieghan Killackey, Gillian Backlin, et al.
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