Immunohematology (29)
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Rh disease in Mexico: evaluating regional and institutional differences in treatment availability and disease management
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CD36 antibodies in isoimmunised African-origin pregnant women: three years’ experience in Spain
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ELP protocol: an original approach for the mitigation of anti-CD38 interference
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Description of the first case of c.137-8C>T GYPB mutation not associated to the GYPB(P2) allele
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Defining the breakpoints of hybrid blood group alleles
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Single-exon fetal RHD genotyping: a 31-month follow up in the obstetric population of Western Sweden
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Patients with red cell antibodies: registries improve patient care by increasing patient safety, reducing costs, and enabling health information exchange
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Genomic characterisation of clinically significant blood group variants in Aboriginal Australians
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Noninvasive fetal blood group antigen genotyping
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First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa
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Characterization of GYP(B-A-B) hybrid glycophorins among Thai blood donors with Mia-positive phenotypes
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Pretreatment with Daudi cells eliminates anti-CD47 monoclonal antibody interference in immunohematology testing
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Use of a recombinant deacetylase to convert A1 red blood cells to the acquired B phenotype for quality control purposes
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Aplastic anemia after SARS-CoV-2 infection or vaccines: case series and literature review
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Breakpoint regions of an RHD-CE(4-9)-D allele and a rare JK allele in a Pacific Islander individual
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A novel method for antibody specificity identification using microscale direct antiglobulin test-positive red cells
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Genetic and mechanistic evaluation of an individual with para-Bombay phenotype associated with a compound heterozygote comprising two novel FUT1 variants
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A voluntary transfusion recipient registry in Korea as a database for blood group antibodies
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Significant neutropenia induced by metamizole dependent neutrophil antibodies
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Prevention and treatment of COVID-19 by mono- and poly-clonal antibodies
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Evaluation of an automated platform for non-invasive single-exon fetal RHD genotyping early in pregnancy
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A rare case of congenital amegakaryocytic thrombocytopenia associated with possible neonatal alloimmune thrombocytopenia and neutropenia by anti-HLA antibodies
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Identification of an Alu-mediated 5.7-kb deletion of the LU gene in a pregnant Moroccan woman with anti-Lu3
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Serologically D-negative blood donors in Thailand: molecular variants and diagnostic strategy
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When the available blood supply mismatches the needs of the patient
29 Items