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Blood|November 19, 2011
Fetal hemoglobin levels and morbidity in untransfused patients with β-thalassemia intermediaKhaled M Musallam, Vijay G Sankaran, Maria Domenica Cappellini, et al.Plos One|February 3, 2017
NNKTT120, an anti-iNKT cell monoclonal antibody, produces rapid and sustained iNKT cell depletion in adults with sickle cell diseaseJoshua J Field, Elaine Majerus, Kenneth I Ataga, et al.Blood|October 24, 2002
A novel diagnostic screen for defects in the Fanconi anemia pathwayAkiko Shimamura, Rocio Montes de Oca, John L Svenson, et al.Transactions of the American Clinical and Climatological Association|January 11, 2013
Sickle cell disease (SCD), iNKT cells, and regadenoson infusionDavid G Nathan, Joshua Field, Gene Lin, et al.Blood|April 17, 2010
Pulmonary hypertension and nitric oxide depletion in sickle cell diseaseH Franklin Bunn, David G Nathan, George J Dover, et al.Blood|February 5, 2013
Sickle cell vaso-occlusion causes activation of iNKT cells that is decreased by the adenosine A2A receptor agonist regadenosonJoshua J Field, Gene Lin, Maureen M Okam, et al.The Journal of Clinical Investigation|June 19, 2012
Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemiaVijay G Sankaran, Roxanne Ghazvinian, Ron Do, et al.Lancet (London, England)|May 16, 2003
Effectiveness and safety of ICL670 in iron-loaded patients with thalassaemia: a randomised, double-blind, placebo-controlled, dose-escalation trialEric Nisbet-Brown, Nancy F Olivieri, Patricia J Giardina, et al.Blood Advances|January 4, 2018
Randomized phase 2 trial of regadenoson for treatment of acute vaso-occlusive crises in sickle cell diseaseJoshua J Field, Elaine Majerus, Victor R Gordeuk, et al.British Journal of Haematology|September 24, 2004
RNA and protein evidence for haplo-insufficiency in Diamond-Blackfan anaemia patients with RPS19 mutationsHanna T Gazda, Rong Zhong, Lilia Long, et al.Pageof 6