Immunohematology (47)
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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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The -72G>A nucleotide substitution impairs transcription of the ABO gene via reduction of promoter activity
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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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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
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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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A novel serological RhD confirmatory test for patients with warm autoimmune haemolytic anaemia with a strong positive direct antiglobulin test
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Prenatal screening service for fetal RHD genotyping to guide prophylaxis: the two-year experience of the Friuli Venezia Giulia region in Italy
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From the investigation of RHD-CE hybrid genes to the recognition of RHCE variants and RHD zygosity. Expanding the analysis by QMPSF in Brazilian donors and in patients with sickle cell disease
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Performance evaluation study of ID CORE XT, a high throughput blood group genotyping platform
47 Items