Immunohematology (62)
All Items
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Erratum to: Rhnull phenotype caused by a novel RHAG allele, RHAG*c.640+1G>C, in a Chinese individual: A novel Rhnull phenotype caused by RHAG*c.640+1G>C
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IgA driven autoimmune hemolytic anemia: a monocentric Italian report and literature review: Management of IgA mediated AIHA
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The 2 breakpoint regions of an RHCE-D(2-9)-CE allele causing a D-- phenotype and its RhAG antigen density: RHCE-D(2-9)-CE hybrid allele and RhAG density
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Distribution of human platelet antigen genotypes in Lithuanian blood donors: HPA genotypes in Lithuanian donors
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Standardized diagnostic approach for cold agglutinin disease: results from a Delphi-Based Expert Consensus: Diagnostic consensus for cold agglutinin disease
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Variation in eluate volume during DNA extraction does not affect eluate concentration of plasma-derived DNA: Eluate variation and plasma-derived DNA
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RBCs of Asian-type DEL do not undergo antibody-mediated phagocytosis by macrophages: Asian DEL RBCs resist macrophage phagocytosis
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Establishment of a high-resolution melting assay for detection of GYP*Mur allele zygosity: HRM assay for GYP*Mur zygosity
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The RHCE*CeRN allele: molecular junction characterization and frequency distribution in Sub-Saharan African populations: Sequencing the CeRN allele
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Serology and molecular genetic analysis of weakened expression of ABO blood group antigens in Chinese pediatric population: Genetic analysis of weak ABO antigens
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Rhnull phenotype caused by a novel RHAG allele, RHAG*c.640+1G>C, in a Chinese individual: A novel Rhnull phenotype caused by RHAG*c.640+1G>C
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Results of red cell antibody screening assays from 2,500 laboratories in 10 external quality assessment programs: sensitivity for anti-D: Sensitivity of red cell antibody detection
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Identification of a novel B allele with c.298T>A giving rise to a weak B phenotype in Chinese voluntary blood donors: Novel B allele c.298T>A in weak B phenotype
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Irregular antibodies in pregnancy during the universal anti-RHD prophylaxis era: a survey of Spanish Hospitals: Irregular antibodies during pregnancy in Spain
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Identification and analysis of a novel ABO allele with c.959insC variant in a Chinese blood donor: A novel ABO c.959insC allele in a Chinese blood donor
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Molecular mechanism of a novel Aweak subtype in Chinese pedigrees: identification and analysis of a large genomic deletion in the promoter upstream distal region of the ABO gene: Aweak from ABO promoter upstream deletion
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RH gene inversion-recombination as a major mechanism of the D-- phenotype in China: Complex RH structural variant in Chinese D-- phenotype
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Molecularly confirmed para-Bombay (Ah) secretor phenotype with FUT1 c.328G>A and FUT2 c.357C>T mutations: first case report from India: Para-Bombay Ah secretor phenotype from India
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Complete D epitope expression of the most common weak D types 15, 25, 33, and 72 in the Chinese population: Strategy for Chinese common weak D
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Neonatal alloimmune thrombocytopenia due to anti-HPA-1b and anti-HLA antibodies: diagnostic and transfusion management of a clinical case: Diagnostic tools to guide FNAIT management
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Multicenter evaluation of soluble CD38: neutralizing anti-CD38 pan-reactivity to enable alloantibody detection: CD38 pretreatment: a key to alloantibody detection
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Passive transfer of silent red blood cell autoantibodies via the placenta and breast milk: a case report: Silent RBC autoantibodies in neonatal plasma and maternal breast milk
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Non-invasive fetal HPA genotyping by UMI-NGS: a robust method for antenatal diagnosis including 48 fetal DNA markers: Non-invasive fetal HPA genotyping by UMI-NGS
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A novel A allele with c.575T>C variant in glycosyltransferase A leads to ABO discrepancy: c.575T>C: new A allele linked to ABO discrepancy
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Delayed hemolytic transfusion reaction associated with anti-Au(a) antibody in a young male with beta-thalassemia: Anti-Au(a) associated hemolytic reaction
62 Items
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