A case of megaloblastic anemia simulating a cold autoimmune hemolytic anemia
De La Puerta, R., Carpio, N., Sanz, G., Solves, P.
Prevalence of DEL phenotype in D– blood donors in India
Chaudhary, R., Verma, S., Verma, A.
Blood component administration to multiple myeloma patients treated with daratumumab: suggesting a novel approach with use of 0.1 M dithiothreitol
Pandey, P., Setya, D., Kaul, E., Ranjan, S., Singh, M.K., Shankar, A.
Concordance of two polymerase chain reaction–based blood group genotyping platforms for patients with sickle cell disease
Sheppard, C.A., Bolen, N.L., Meny, G., Kalvelage, M., Ochoa-Garay, G.
Routine indirect antiglobulin testing of blood donors—a further step toward blood safety: an experience from a tertiary care center in northern India
Malhotra, S., Negi, G., Kaur, D., Meinia, S.K., Tiwari, A.K., Mitra, S.
Two Thai Burmese descendants with A4GALT*01N.21, p phenotype, and anti-PP1Pk
Intharanut, K., Sasikarn, W., Chusri, W., Nathalang, O.
Identification of rare blood types in southern Brazil: impact on transfusion support
de Araújo, C.D.S.R., Machado, B.A., Reche, C.D., Maroni, L., Garlet, L.C., dos Santos, M.M.P., Beber, M., Pasqualotti, A., Castilho, L.
Identifying obstetrics patients in whom RHD genotyping can be used to assess risk of D alloimmunization
Horn, T.N., Keller, J., Keller, M.A., Klinger, L.
Cover_TOC_Masthead - ISSUE 2/2020
An update on the RAPH blood group system
Keller, M.A.
Weak D types 38 and 11: determination of frequencies in a Brazilian population and validation of an easy molecular assay for detection
Dezan, M.R., Oliveira, V.B., Conrado, M., Luz, F., Gallucci, A., Oliveira, T.G.M., Sabino, E.C., Rocha, V., Mendrone, A., Dinardo, C.L.
A prospective, observational study for optimization of antibody screening in pretransfusion compatibility testing
Pandey, P., Setya, D., Srivastava, R., Singh, M.K.