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T D Coates

Showing results (41-50 of 58) with videos related to

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The New England Journal of Medicine|October 15, 1987
Treatment of antibody-mediated pure red-cell aplasia with high-dose intravenous gamma globulinW A McGuire, H H Yang, E Bruno, et al.
The New England Journal of Medicine|August 12, 1982
Lactoferrin deficiency associated with altered granulocyte functionL A Boxer, T D Coates, R A Haak, et al.
Blood|June 1, 1982
Metabolic, membrane, and functional responses of human polymorphonuclear leukocytes to platelet-activating factorL M Ingraham, T D Coates, J M Allen, et al.
Progress in Clinical and Biological Research|January 1, 1983
Role of nutrition support in the management of children with cancerK A Rickard, T D Coates, J L Grosfeld, et al.
Cancer Research|January 1, 1982
Supportive nutritional intervention in pediatric cancerK A Rickard, R L Baehner, T D Coates, et al.
Haematology and Blood Transfusion|January 1, 1985
Advances in parenteral nutrition support of children with neoplastic diseasesK A Rickard, J L Grosfeld, T D Coates, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|January 1, 1991
Qualitative functional deficiency of affinity-purified lactoferrin from neutrophils of patients with chronic myelogenous leukemia, and lactoferrin/H-ferritin-cell interactions in a patient with lactoferrin-deficiency with normal numbers of circulating leukocytesH E Broxmeyer, D C Bicknell, S Cooper, et al.
Cancer Research|January 1, 1989
Pharmacology studies of 1-beta-D-arabinofuranosylcytosine in pediatric patients with leukemia and lymphoma after a biochemically optimal regimen of loading bolus plus continuous infusion of the drugV I Avramis, K I Weinberg, J K Sato, et al.
Clinical Hemorheology and Microcirculation|April 6, 2010
Sickle cell disease: selected aspects of pathophysiologyT Alexy, S Sangkatumvong, P Connes, et al.
Blood|March 1, 1985
Glycoprotein-180 deficiency: genetics and abnormal neutrophil activationS J Weisman, R L Berkow, G Plautz, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
The New England Journal of Medicine|October 15, 1987
Treatment of antibody-mediated pure red-cell aplasia with high-dose intravenous gamma globulinW A McGuire, H H Yang, E Bruno, et al.
The New England Journal of Medicine|August 12, 1982
Lactoferrin deficiency associated with altered granulocyte functionL A Boxer, T D Coates, R A Haak, et al.
Blood|June 1, 1982
Metabolic, membrane, and functional responses of human polymorphonuclear leukocytes to platelet-activating factorL M Ingraham, T D Coates, J M Allen, et al.
Progress in Clinical and Biological Research|January 1, 1983
Role of nutrition support in the management of children with cancerK A Rickard, T D Coates, J L Grosfeld, et al.
Cancer Research|January 1, 1982
Supportive nutritional intervention in pediatric cancerK A Rickard, R L Baehner, T D Coates, et al.
Haematology and Blood Transfusion|January 1, 1985
Advances in parenteral nutrition support of children with neoplastic diseasesK A Rickard, J L Grosfeld, T D Coates, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|January 1, 1991
Qualitative functional deficiency of affinity-purified lactoferrin from neutrophils of patients with chronic myelogenous leukemia, and lactoferrin/H-ferritin-cell interactions in a patient with lactoferrin-deficiency with normal numbers of circulating leukocytesH E Broxmeyer, D C Bicknell, S Cooper, et al.
Cancer Research|January 1, 1989
Pharmacology studies of 1-beta-D-arabinofuranosylcytosine in pediatric patients with leukemia and lymphoma after a biochemically optimal regimen of loading bolus plus continuous infusion of the drugV I Avramis, K I Weinberg, J K Sato, et al.
Clinical Hemorheology and Microcirculation|April 6, 2010
Sickle cell disease: selected aspects of pathophysiologyT Alexy, S Sangkatumvong, P Connes, et al.
Blood|March 1, 1985
Glycoprotein-180 deficiency: genetics and abnormal neutrophil activationS J Weisman, R L Berkow, G Plautz, et al.
Pageof 6