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Blood|September 17, 2005
Pathology of Berkeley sickle cell mice: similarities and differences with human sickle cell diseaseElizabeth A Manci, Cheryl A Hillery, Carol A Bodian, et al.The Journal of Pediatrics|June 8, 2001
Bleeding disorders: A common cause of menorrhagia in adolescentsJ A Bevan, K W Maloney, C A Hillery, et al.Blood|August 30, 2003
Increased erythrocyte adhesion in mice and humans with hereditary spherocytosis and hereditary elliptocytosisNancy J Wandersee, Scott C Olson, Sandra L Holzhauer, et al.British Journal of Haematology|August 20, 2016
Substance P is increased in patients with sickle cell disease and associated with haemolysis and hydroxycarbamide useAmanda M Brandow, Nancy J Wandersee, Mahua Dasgupta, et al.British Journal of Haematology|May 21, 2011
Methaemalbumin formation in sickle cell disease: effect on oxidative protein modification and HO-1 inductionMadelyn S Hanson, Barbora Piknova, Agnes Keszler, et al.Plos One|December 29, 2015
R-Ras Regulates Murine T Cell Migration and Intercellular Adhesion Molecule-1 BindingXiaocai Yan, Mingfei Yan, Yihe Guo, et al.Blood|June 15, 1997
Mechanisms of stroke in sickle cell disease: sickle erythrocytes decrease cerebral blood flow in rats after nitric oxide synthase inhibitionJ A French, D Kenny, J P Scott, et al.Pain|April 27, 2018
Chemokine (c-c motif) receptor 2 mediates mechanical and cold hypersensitivity in sickle cell disease miceKatelyn E Sadler, Katherine J Zappia, Crystal L O'Hara, et al.Pediatric Blood & Cancer|January 21, 2014
Intravenous magnesium for pediatric sickle cell vaso-occlusive crisis: methodological issues of a randomized controlled trialOluwakemi Badaki-Makun, J Paul Scott, Julie A Panepinto, et al.Blood|June 29, 2011
Transient receptor potential vanilloid 1 mediates pain in mice with severe sickle cell diseaseCheryl A Hillery, Patrick C Kerstein, Daniel Vilceanu, et al.Pageof 7