Posters on the topic "Immunohematology"

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  • P-7-1
  • Poster
Software update enables improved RHCE/RHD genotyping on allele level for real-time PCR system
  • Sabrina König (Kronberg / DE)
  • P-7-10
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Residual risk of hemolytic transfusion reaction by release of red blood cell concentrated by type and screen: 16 years' experience
  • P-7-11
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First red cell panel for alloantibody differentiation available in Northern Nigeria
  • P-7-12
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Characterization of anti-PF4 monoclonal antibodies to study vaccine-induced immune thrombocytopenia and thrombosis
  • P-7-13
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Intravenous immunoglobulins prevent thrombus formation in an ex vivo microfluidic disease model of HIT
  • P-7-14
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Anti-RH1 in a Patient with Weak RH1 Type 2 Genotype: A Case Report
  • P-7-15
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Utilizing an automated hollow-fiber perfusion system for large-scale expansion of suspension cells
  • P-7-16
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Case-Report: A Case of Hemolytic Disease of the Newborn (HDN) Due to Anti-Wr(a)
  • P-7-17
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Anti-HPA-1a alloantibody-mediated mechanisms of platelet destruction in fetal-neonatal alloimmune thrombocytopenia may be more complex than "eating up"
  • P-7-18
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ABO- incompatible stem cell transplantation with pre-existing donor specific HLA and red blood cell antibodies
  • P-7-19
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Long-read sequencing to characterize conspicuous ABO null alleles
  • P-7-2
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High isoagglutinin titers in platelet concentrates: a cause for positive red blood cell crossmatch
  • P-7-20
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Fetal RHD detection from maternal plasma – comparison of two assays developed according to the "Workshop report on extraction of fetal DNA from maternal plasma"
  • P-7-21
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Validation of a new commercial kit for fetal RHD detection from maternal plasma
  • P-7-22
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Predictive parameters for the isolation of platelets from whole blood for diagnostic purposes in patients with immune thrombocytopenia
  • P-7-23
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Autoantibodies in the serum of donors: Can TRALI be expected?
  • P-7-24
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Haplotype phasing by long read nanopore sequencing of the CR1 gene coding for the Knops blood group system
  • P-7-25
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Challenge of RhCE typing due to existing variants on both alleles: A report on two cases
  • P-7-26
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First experience with Anti-CD47 therapy in transfusion medicine
  • P-7-27
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A case of de novo alloimmunisation under daratumumab therapy
  • P-7-28
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IgG antibody screening assays with an automated sample dilution
  • P-7-29
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Normalization of platelet count is not related to the amount of transfused platelets in neonatal alloimmune thrombocytopenia – Report of a case series with three neonates
  • P-7-3
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Identification of Two Novel ABO Blood Group Alleles
  • P-7-30
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Detection of blood group A antigen in Bombay blood group Oh after oral fucose therapy in a rare case of Leukocyte Adhesion Deficiency Type II (LAD II)
  • P-7-31
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Obvious and unexpected problems in a massive transfusion of a patient with Anti-Lub antibodies
  • P-7-4
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Detection of Autoanti-Scianna Utilizing Recombinant Blood Group Antigens
  • P-7-5
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Resolving RhD typing discrepancies by the LightCycler® PRO instrument
  • P-7-6
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Characterization of two novel RHD variant alleles
  • P-7-7
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A p.Glu419Asp missense mutation causes a weak expression of KEL1
  • P-7-8
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Frequency of various rare blood group antigens, ABO, Rhesus Blood grouping and its Relations to occurrence of stillbirth, Miscarriage and transfusion status among Pregnant Women in University of Calabar, Calabar, Nigeria
  • P-7-9
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A survey on the clinical routine of the "biological test" (Oehlecker's test) in German speaking countries
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