Search Results - Lougaris, Vassilis

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  1. 1
    Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

    Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes by Salzer, Ulrich, Bacchelli, Chiara, Buckridge, Sylvie, Pan-Hammarström, Qiang, Jennings, Stephanie, Lougaris, Vassilis, Bergbreiter, Astrid, Hagena, Tina, Birmelin, Jennifer, Plebani, Alessandro, Webster, A. David B., Peter, Hans-Hartmut, Suez, Daniel, Chapel, Helen, McLean-Tooke, Andrew, Spickett, Gavin P., Anover-Sombke, Stephanie, Ochs, Hans D., Urschel, Simon, Belohradsky, Bernd H., Ugrinovic, Sanja, Kumararatne, Dinakantha S., Lawrence, Tatiana C., Holm, Are M., Franco, Jose L., Schulze, Ilka, Schneider, Pascal, Gertz, E. Michael, Schäffer, Alejandro A., Hammarström, Lennart, Thrasher, Adrian J., Gaspar, H. Bobby, Grimbacher, Bodo

    Published in Blood
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  2. 2
    Screening of functional and positional candidate genes in families with common variable immunodeficiency

    Screening of functional and positional candidate genes in families with common variable immunodeficiency by Salzer, Ulrich, Neumann, Carla, Thiel, Jens, Woellner, Cristina, Pan-Hammarström, Qiang, Lougaris, Vassilis, Hagena, Tina, Jung, Johannes, Birmelin, Jennifer, Du, Likun, Metin, Ayse, Webster, David A, Plebani, Alessandro, Moschese, Viviana, Hammarström, Lennart, Schäffer, Alejandro A, Grimbacher, Bodo

    Published in BMC immunology
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  3. 3
    Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiency

    Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiency by Kutukculer, Necil, Moratto, Daniele, Aydinok, Yesim, Lougaris, Vassilis, Aksoylar, Serap, Plebani, Alessandro, Genel, Ferah, Notarangelo, Luigi D.

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  4. 4
    Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency

    Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency by SORESINA, Annarosa, LOUGARIS, Vassilis, GILIANI, Silvia, CARDINALE, Fabio, ARMENIO, Lucio, CATTALINI, Marco, NOTARANGELO, Luigi D, PLEBANI, Alessandro

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