Showing results (31-40 of 2,141) with videos related to
Sort By:
Pageof 215
International Journal of Laboratory Hematology|February 7, 2018
Pre-analytical stability of coagulation parameters in plasma stored at room temperatureE A Linskens, K M J DevreeseInternational Journal of Laboratory Hematology|March 25, 2018
Flow cytometric osmotic fragility test and eosin-5'-maleimide dye-binding tests are better than conventional osmotic fragility tests for the diagnosis of hereditary spherocytosisR D Arora, J Dass, S Maydeo, et al.International Journal of Laboratory Hematology|March 7, 2018
Coexistence of JAK2 or CALR mutation is a rare but clinically important event in chronic myeloid leukemia patients treated with tyrosine kinase inhibitorsK Lewandowski, M Gniot, M Wojtaszewska, et al.International Journal of Laboratory Hematology|February 25, 2018
Prenatal diagnosis in rare bleeding disorders-An unresolved issue?S Tabibian, M Shams, M Naderi, et al.International Journal of Laboratory Hematology|February 11, 2018
Comprehensive re-evaluation of historical von Willebrand disease diagnosis in association with whole blood platelet aggregation and functionV Nummi, R Lassila, L Joutsi-Korhonen, et al.International Journal of Laboratory Hematology|March 8, 2018
Stability of complete blood count in different storage conditions using the ABX PENTRA 60 analyzerL R Oliveira, M Simionatto, B R Cruz, et al.International Journal of Laboratory Hematology|January 4, 2019
Development of new methodologies for the chromogenic estimation of betrixaban concentrations in plasmaRomain Siriez, Jonathan Evrard, Jean-Michel Dogné, et al.International Journal of Laboratory Hematology|July 10, 2007
Molecular genetic analysis of haematological malignancies II: Mature lymphoid neoplasmsA J Bench, W N Erber, G A Follows, et al.International Journal of Laboratory Hematology|July 10, 2007
Robust, routine haematology reference ranges for healthy adultsL Wakeman, S Al-Ismail, A Benton, et al.International Journal of Laboratory Hematology|July 10, 2007
Sickle cell-haemoglobin E (HbSE) compound heterozygosity: a clinical and haematological studyH H M Knox-Macaulay, M M Ahmed, D Gravell, et al.Pageof 215