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The American Journal of Cardiology|September 17, 2013
Effect of extended-release niacin on serum lipids and on endothelial function in adults with sickle cell anemia and low high-density lipoprotein cholesterol levelsHeather M Scoffone, Megan Krajewski, Suzana Zorca, et al.European Journal of Haematology|April 9, 2013
Clinical correlates of acute pulmonary events in children and adolescents with sickle cell diseaseRabindra Paul, Caterina P Minniti, Mehdi Nouraie, et al.American Journal of Respiratory and Critical Care Medicine|September 10, 2019
Platelet Extracellular Vesicles Drive Inflammasome-IL-1β-Dependent Lung Injury in Sickle Cell DiseaseRavi Vats, Tomasz Brzoska, Margaret F Bennewitz, et al.Alimentary Pharmacology & Therapeutics|August 4, 2015
Liver injury is associated with mortality in sickle cell diseaseJ J Feld, G J Kato, C Koh, et al.Chemical Biology & Drug Design|October 25, 2018
Design, synthesis and antitrypanosomatid activities of 3,5-diaryl-isoxazole analogues based on neolignans veraguensin, grandisin and machilin GOzildéia S Trefzger, Amarith R das Neves, Natália V Barbosa, et al.Scientific Reports|August 27, 2021
Phytochemistry reflects different evolutionary history in traditional classes versus specialized structural motifsKathryn A Uckele, Joshua P Jahner, Eric J Tepe, et al.American Journal of Hematology|October 19, 2013
A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemiaInna Belfer, Victoria Youngblood, Deepika S Darbari, et al.Cell Reports|January 30, 2026
Leveraging current steering and the biophysics of spike generation for cellular-resolution electrical stimulation of neuronsPraful K Vasireddy, Ramandeep S Vilkhu, Amrith Lotlikar, et al.Haematologica|March 19, 2026
Phase I study of the safety and pharmacokinetics of CSL889 (hemopexin) in adults with sickle cell anemiaBart J Biemond, Rachel Kesse-Adu, Ezanul Wahab, et al.Haematologica|October 14, 2011
Pulmonary artery pressure and iron deficiency in patients with upregulation of hypoxia sensing due to homozygous VHL(R200W) mutation (Chuvash polycythemia)Craig A Sable, Zakari Y Aliyu, Niti Dham, et al.Pageof 82