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British Journal of Haematology|May 8, 1999
Born to clot: the European burdenD C Rees, N H Chapman, M T Webster, et al.
Blood Cells, Molecules & Diseases|March 6, 2014
Effects of o-vanillin on K⁺ transport of red blood cells from patients with sickle cell diseaseA Hannemann, U M C Cytlak, O T Gbotosho, et al.
Blood Cells, Molecules & Diseases|March 16, 2010
Novel permeability characteristics of red blood cells from sickle cell patients heterozygous for HbS and HbC (HbSC genotype)S Dalibalta, J C Ellory, J A Browning, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1986
Structural homology of reaction centers from Rhodopseudomonas sphaeroides and Rhodopseudomonas viridis as determined by x-ray diffractionJ P Allen, G Feher, T O Yeates, et al.
Blood|January 1, 1997
Erythroblastic inclusions in dominantly inherited beta thalassemiasP J Ho, S N Wickramasinghe, D C Rees, et al.
British Journal of Haematology|December 1, 1995
The metabolites of nitric oxide in sickle-cell diseaseD C Rees, P Cervi, D Grimwade, et al.
The Journal of Physiology|January 9, 2013
A non-electrolyte haemolysis assay for diagnosis and prognosis of sickle cell diseaseC Milligan, D C Rees, J C Ellory, et al.
Geriatric Nursing (New York, N.Y.)|May 14, 2020
Factors associated with signs of aspiration in older adults: A prospective studyDai Pu, Edwin M L Yiu, Karen M K Chan
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