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Clinical and Laboratory Haematology|February 15, 2002
Haemoglobin Pierre-Benite--a high affinity variant associated with relative polycythaemiaM E Beard, H C Potter, R L Spearing, et al.Clinical and Laboratory Haematology|February 15, 2002
Audit of anticoagulant therapy and acute hospital admissionsH M Hirri, P J GreenClinical and Laboratory Haematology|March 1, 1996
Laboratory evaluation of a new delivery system to improve patient compliance with chelation therapyT Lombardo, V Frontini, G Ferro, et al.Clinical and Laboratory Haematology|March 1, 1996
Benign familial macrocytosisL A Sechi, S De Carli, C Catena, et al.Clinical and Laboratory Haematology|March 1, 1996
Abrupt cessation of immunosuppression in a patient with persistent acute lymphoblastic leukaemia following allogeneic transplantationN L Rymes, J A Murray, J A HolmesClinical and Laboratory Haematology|March 1, 1996
The effect of GM-CSF on reticulocytes, haemoglobin and haematocrit in patients receiving chemotherapy for solid tumoursG S Paterakis, N Tsavaris, D LoukopoulosClinical and Laboratory Haematology|September 1, 1996
Usefulness of flow cytometric detection of cell surface interleukin-6 receptors in human myeloma cell linesY H Chen, X X Feng, K HagenClinical and Laboratory Haematology|September 1, 1996
An evaluation of the CELL-DYN 1700 haematology analyser: automated cell counting and three-part leucocyte differentiationC Sachse, E HenkelClinical and Laboratory Haematology|April 10, 1999
Artefactual elevation of an automated white cell count following femoral vein punctureA J Whiteway, B J BainClinical and Laboratory Haematology|January 1, 1992
Haematological phenotypes in a family with triplicated alpha-globin gene, beta zero 39 and delta+27 thalassaemia mutationsL Oggiano, E Rimini, L Frogheri, et al.Pageof 129