Characterization of the novel HLA‐DPB11219:01 allele by next‐generation sequencing von Scherer, Vanessa, Flesch, Brigitte K.

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Compound heterozygosity induces a rare Gerbich‐negative phenotype in an immunized blood donor von Petermann, Sarah, Mayer, Vanessa, Carbol, Alexander, Opitz, Andreas, Flesch, Brigitte K.

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Multicenter Study on Differential Human Neutrophil Antigen 2 Expression and Underlying Molecular Mechanisms von Flesch, Brigitte K., Reil, Angelika, Nogués, Núria, Canals, Carme, Bugert, Peter, Schulze, Torsten J., Huiskes, Elly, Porcelijn, Leendert, Höglund, Petter, Ratcliffe, Paul, Schönbacher, Marlies, Kerchrom, Hans, Kellershohn, Josina, Bayat, Behnaz

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Expression of the CTL2 transcript variants in human peripheral blood cells and human tissues von Flesch, Brigitte K., Wesche, Jan, Berthold, Tom, Goldmann, Torsten, Hundt, Matthias, Greinacher, Andreas, Bux, Jürgen

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Amino Acid Polymorphisms in Hla Class II Differentiate Between Thyroid and Polyglandular Autoimmunity von Frommer, Lara, Flesch, Brigitte K, König, Jochem, Kahaly, George J

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Platelet CD36 deficiency is present in 2.6% of Arabian individuals and can cause NAIT and platelet refractoriness von Flesch, Brigitte K., Scherer, Vanessa, Opitz, Andreas, Ochmann, Oswin, Janson, Anne, Steitz, Monika, Zeiler, Thomas

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Sex Alters the MHC Class I HLA-A Association With Polyglandular Autoimmunity von Flesch, Brigitte K, König, Jochem, Frommer, Lara, Hansen, Martin P, Kahaly, George J

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Transfusion‐related acute lung injury caused by human leucocyte antigen class II antibody von Flesch, Brigitte K., Neppert, Jürgen

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Update on the nomenclature of human neutrophil antigens and alleles von Flesch, Brigitte K., Curtis, Brian R., de Haas, Masja, Lucas, Geoff, Sachs, Ulrich J.

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HNA-1d: a new human neutrophil antigen located on Fcγ receptor IIIb associated with neonatal immune neutropenia von Reil, Angelika, Sachs, Ulrich J., Siahanidou, Tania, Flesch, Brigitte K., Bux, Juergen

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Genetic variation of the HNA-3a encoding gene von Flesch, Brigitte K., Reil, Angelika, Bux, Jürgen

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A serologic weakly reactive RhD is caused by a RHD 374T>A (Ile125Asn) von Flesch, Brigitte K., Schottstedt, Volkmar, Spallek, Heinrich, Just, Burkhard

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FCGR3 variants and expression of human neutrophil antigen-1a, -1b, and -1c in the populations of northern Germany and Uganda von Flesch, Brigitte K., Doose, Sandra, Siebert, Reiner, Ntambi, Elisabeth, Neppert, Juergen

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The AQP1 del601G mutation in different European Romani (Gypsy) populations von Flesch, Brigitte K, Morar, Bharti, Comas, David, Muñiz-Diaz, Eduardo, Nogués, Núria, Kalaydjieva, Luba

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Paired crossover study of two plateletpheresis systems concerning platelet product quality and donor comfort von Flesch, Brigitte K., Adamzik, Ilse, Steppat, Dagmar, Miller, Joanna, Carstensen, Liane, Schapke, Martin, Davey, Jason

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The AQP1 mutation c.601delG causes the Co-negative phenotype in four patients belonging to the Romani (Gypsy) ethnic group von Flesch, Brigitte K, Just, Burkhard, Deitenbeck, Robert, Reil, Angelika, Bux, Jürgen, Nogués, Núria, Muñiz-Diaz, Eduardo

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Characterization of the novel HLA‐DPB1 1219:01 allele by next‐generation sequencing von Scherer, Vanessa, Flesch, Brigitte K.

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Variant FCGR3 genes: transcription and possible origins von Tong, Yin, Jin, Jie, Marget, Matthias, Humpe, Andreas, Neppert, Juergen, Flesch, Brigitte K

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FCGR3B gene frequencies and FCGR3 variants in a Chinese population from Zhejiang Province von Tong, Yin, Jin, Jie, Yan, Lixing, Neppert, Jürgen, Marget, Matthias, Flesch, Brigitte K

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Expression of the CTL 2 transcript variants in human peripheral blood cells and human tissues von Flesch, Brigitte K., Wesche, Jan, Berthold, Tom, Goldmann, Torsten, Hundt, Matthias, Greinacher, Andreas, Bux, Jürgen

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