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Molecular Pharmacology|May 1, 1983
Identification of 2-imidazolines as anti-sickling agentsH Chang, S M Ewert, R L NagelBlood|April 1, 1983
Comparative evaluation of fifteen anti-sickling agentsH Chang, S M Ewert, R M Bookchin, et al.The Journal of Clinical Investigation|December 1, 1982
SC erythrocytes have an abnormally high intracellular hemoglobin concentration. Pathophysiological consequencesM E Fabry, D K Kaul, C Raventos-Suarez, et al.Current Opinion in Hematology|February 27, 2001
Pleiotropic and epistatic effects in sickle cell anemiaR L NagelCellular and Molecular Biology (Noisy-Le-Grand, France)|March 26, 2004
Beta-globin-gene haplotypes, mitochondrial DNA, the Y-chromosome: their impact on the genetic epidemiology of the major structural hemoglobinopathiesR L NagelComptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|February 27, 1999
Will the genetic individualization of disease force a new paradigm?R L NagelHematology/Oncology Clinics of North America|June 1, 1991
The distinct pathobiology of sickle cell-hemoglobin C disease. Therapeutic implicationsR L Nagel, C LawrenceThe Journal of Biological Chemistry|March 10, 1981
Esterase activity of hemoglobin. Differences between HB A and HB SD Elbaum, R L NagelPageof 597