CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency von van Zelm, Menno C, Smet, Julie, Adams, Brigitte, Mascart, Françoise, Schandené, Liliane, Janssen, Françoise, Ferster, Alina, Kuo, Chiung-Chi, Levy, Shoshana, van Dongen, Jacques J M, van der Burg, Mirjam

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Targeted next-generation sequencing: A novel diagnostic tool for primary immunodeficiencies von Nijman, Isaac J., PhD, van Montfrans, Joris M., MD, PhD, Hoogstraat, Marlous, BAS, Boes, Marianne L., PhD, van de Corput, Lisette, PhD, Renner, Ellen D., MD, PhD, van Zon, Patrick, BSc, van Lieshout, Stef, BSc, Elferink, Martin G., PhD, van der Burg, Mirjam, PhD, Vermont, Clementien L., MD, PhD, van der Zwaag, Bert, PhD, Janson, Esther, BSc, Cuppen, Edwin, PhD, Ploos van Amstel, Johannes K., PhD, van Gijn, Marielle E., PhD

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Increased PI3K/Akt activity and deregulated humoral immune response in human PTEN deficiency von Driessen, Gertjan J., MD, PhD, IJspeert, Hanna, PhD, Wentink, Marjolein, MD, Yntema, Helger G., MD, PhD, van Hagen, P. Martin, MD, PhD, van Strien, Arthur, MSc, Bucciol, Giorgia, MD, Cogulu, Ozgur, MD, Trip, Margreet, MD, Nillesen, Willy, MD, PhD, Peeters, Els A., MD, PhD, Pico-Knijnenburg, Ingrid, BSc, Barendregt, Barbara H., BSc, Rizzi, Marta, MD, PhD, van Dongen, Jacques J., MD, PhD, Kutukculer, Necil, MD, PhD, van der Burg, Mirjam, PhD

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Mutations in the NHEJ Component XRCC4 Cause Primordial Dwarfism von Murray, Jennie E., van der Burg, Mirjam, IJspeert, Hanna, Carroll, Paula, Wu, Qian, Ochi, Takashi, Leitch, Andrea, Miller, Edward S., Kysela, Boris, Jawad, Alireza, Bottani, Armand, Brancati, Francesco, Cappa, Marco, Cormier-Daire, Valerie, Deshpande, Charu, Faqeih, Eissa A., Graham, Gail E., Ranza, Emmanuelle, Blundell, Tom L., Jackson, Andrew P., Stewart, Grant S., Bicknell, Louise S.

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Similar recombination-activating gene ( RAG ) mutations result in similar immunobiological effects but in different clinical phenotypes von IJspeert, Hanna, MSc, Driessen, Gertjan J., MD, PhD, Moorhouse, Michael J., PhD, Hartwig, Nico G., MD, PhD, Wolska-Kusnierz, Beata, MD, Kalwak, Krzysztof, MD, Pituch-Noworolska, Anna, MD, Kondratenko, Irina, MD, van Montfrans, Joris M., MD, PhD, Mejstrikova, Ester, MD, Lankester, Arjan C., MD, PhD, Langerak, Anton W., PhD, van Gent, Dik C., PhD, Stubbs, Andrew P., PhD, van Dongen, Jacques J.M., MD, PhD, van der Burg, Mirjam, PhD

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Case report: Severe combined immunodeficiency with ligase 1 deficiency and Omenn-like manifestation von Dabrowska-Leonik, Nel, Pastorczak, Agata Karolina, Bąbol-Pokora, Katarzyna, Bernat-Sitarz, Katarzyna, Piątosa, Barbara, Heropolitańska-Pliszka, Edyta, Kacprzak, Magdalena M., Kalwak, Krzysztof, Gul, Katarzyna, Burg, Mirjam van der, Ussowicz, Marek, Pac, Malgorzata

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The Euroflow PID Orientation Tube in the diagnostic workup of primary immunodeficiency: Daily practice performance in a tertiary university hospital von Neirinck, Jana, Emmaneel, Annelies, Buysse, Malicorne, Philippé, Jan, Van Gassen, Sofie, Saeys, Yvan, Bossuyt, Xavier, De Buyser, Stefanie, Burg, Mirjam van der, Pérez-Andrés, Martín, Orfao, Alberto, van Dongen, Jacques J. M., Lambrecht, Bart N., Kerre, Tessa, Hofmans, Mattias, Haerynck, Filomeen, Bonroy, Carolien

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XLF deficiency results in reduced N-nucleotide addition during V(D)J recombination von IJspeert, Hanna, Rozmus, Jacob, Schwarz, Klaus, Warren, René L., van Zessen, David, Holt, Robert A., Pico-Knijnenburg, Ingrid, Simons, Erik, Jerchel, Isabel, Wawer, Angela, Lorenz, Myriam, Patıroğlu, Turkan, Akar, Himmet Haluk, Leite, Ricardo, Verkaik, Nicole S., Stubbs, Andrew P., van Gent, Dik C., van Dongen, Jacques J.M., van der Burg, Mirjam

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B-cell development and functions and therapeutic options in adenosine deaminase–deficient patients von Brigida, Immacolata, PhD, Sauer, Aisha V., PhD, Ferrua, Francesca, MD, Giannelli, Stefania, PhD, Scaramuzza, Samantha, PhD, Pistoia, Valentina, MSc, Castiello, Maria Carmina, PhD, Barendregt, Barbara H., BSc, Cicalese, Maria Pia, MD, Casiraghi, Miriam, RCN, Brombin, Chiara, PhD, Puck, Jennifer, MD, Müller, Klaus, MD, PhD, Notarangelo, Lucia Dora, MD, Montin, Davide, MD, van Montfrans, Joris M., MD, PhD, Roncarolo, Maria Grazia, MD, Traggiai, Elisabetta, PhD, van Dongen, Jacques J.M., MD, PhD, van der Burg, Mirjam, PhD, Aiuti, Alessandro, MD, PhD

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Age-associated distribution of normal B-cell and plasma cell subsets in peripheral blood von Blanco, Elena, Pérez-Andrés, Martín, Arriba-Méndez, Sonia, Contreras-Sanfeliciano, Teresa, Criado, Ignacio, Pelak, Ondrej, Serra-Caetano, Ana, Romero, Alfonso, Puig, Noemí, Remesal, Ana, Torres Canizales, Juan, López-Granados, Eduardo, Kalina, Tomas, Sousa, Ana E., van Zelm, Menno, van der Burg, Mirjam, van Dongen, Jacques J.M., Orfao, Alberto

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ATM: Translating the DNA Damage Response to Adaptive Immunity von Weitering, Thomas J., Takada, Sanami, Weemaes, Corry M.R., van Schouwenburg, Pauline A., van der Burg, Mirjam

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Human memory B cells originate from three distinct germinal center-dependent and -independent maturation pathways von Berkowska, Magdalena A., Driessen, Gertjan J.A., Bikos, Vasilis, Grosserichter-Wagener, Christina, Stamatopoulos, Kostas, Cerutti, Andrea, He, Bing, Biermann, Katharina, Lange, Johan F., van der Burg, Mirjam, van Dongen, Jacques J.M., van Zelm, Menno C.

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TREC Based Newborn Screening for Severe Combined Immunodeficiency Disease: A Systematic Review von van der Spek, Jet, Groenwold, Rolf H. H., van der Burg, Mirjam, van Montfrans, Joris M.

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Mutations in Bruton’s tyrosine kinase impair IgA responses von Mitsuiki, Noriko, Yang, Xi, Bartol, Sophinus J. W., Grosserichter-Wagener, Christina, Kosaka, Yoshiyuki, Takada, Hidetoshi, Imai, Kohsuke, Kanegane, Hirokazu, Mizutani, Shuki, van der Burg, Mirjam, van Zelm, Menno C., Ohara, Osamu, Morio, Tomohiro

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An essential role for the Zn2+ transporter ZIP7 in B cell development von Anzilotti, Consuelo, Swan, David J., Boisson, Bertrand, Deobagkar-Lele, Mukta, Oliveira, Catarina, Chabosseau, Pauline, Engelhardt, Karin R., Xu, Xijin, Chen, Rui, Alvarez, Luis, Berlinguer-Palmini, Rolando, Bull, Katherine R., Cawthorne, Eleanor, Cribbs, Adam P., Crockford, Tanya L., Dang, Tarana Singh, Fearn, Amy, Fenech, Emma J., de Jong, Sarah J., Lagerholm, B. Christoffer, Ma, Cindy S., Sims, David, van den Berg, Bert, Xu, Yaobo, Cant, Andrew J., Kleiner, Gary, Leahy, T. Ronan, de la Morena, M. Teresa, Puck, Jennifer M., Shapiro, Ralph S., van der Burg, Mirjam, Chapman, J. Ross, Christianson, John C., Davies, Benjamin, McGrath, John A., Przyborski, Stefan, Santibanez Koref, Mauro, Tangye, Stuart G., Werner, Andreas, Rutter, Guy A., Padilla-Parra, Sergi, Casanova, Jean-Laurent, Cornall, Richard J., Conley, Mary Ellen, Hambleton, Sophie

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Involvement of Artemis in nonhomologous end-joining during immunoglobulin class switch recombination von Du, Likun, van der Burg, Mirjam, Popov, Sergey W, Kotnis, Ashwin, van Dongen, Jacques J M, Gennery, Andrew R, Pan-Hammarström, Qiang

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Universal Newborn Screening for Severe Combined Immunodeficiency (SCID) von van der Burg, Mirjam, Mahlaoui, Nizar, Gaspar, Hubert Bobby, Pai, Sung-Yun

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B Cell Reconstitution and Influencing Factors After Hematopoietic Stem Cell Transplantation in Children von van der Maas, Nicolaas G, Berghuis, Dagmar, van der Burg, Mirjam, Lankester, Arjan C

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A kindred with mutant IKAROS and autoimmunity von Van Nieuwenhove, Erika, Garcia-Perez, Josselyn E., Helsen, Christine, Rodriguez, Princess D., van Schouwenburg, Pauline A., Dooley, James, Schlenner, Susan, van der Burg, Mirjam, Verhoeyen, Els, Gijsbers, Rik, Frietze, Seth, Schjerven, Hilde, Meyts, Isabelle, Claessens, Frank, Humblet-Baron, Stephanie, Wouters, Carine, Liston, Adrian

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The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency von Bigley, Venetia, Haniffa, Muzlifah, Doulatov, Sergei, Wang, Xiao-Nong, Dickinson, Rachel, McGovern, Naomi, Jardine, Laura, Pagan, Sarah, Dimmick, Ian, Chua, Ignatius, Wallis, Jonathan, Lordan, Jim, Morgan, Cliff, Kumararatne, Dinakantha S, Doffinger, Rainer, van der Burg, Mirjam, van Dongen, Jacques, Cant, Andrew, Dick, John E, Hambleton, Sophie, Collin, Matthew

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