Interstitial deletion of chromosome 15: two cases by FORMIGA, L. DE F, POENARU, L, COURONNE, F, FLORI, E, EIBEL, J. L, DEMINATTI, M. M, SAVARY, J. B, LAI, J. L, GILGENKRANTZ, S, PIERSON, M

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B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans by Warnatz, Klaus, Salzer, Ulrich, Rizzi, Marta, Fischer, Beate, Gutenberger, Sylvia, Böhm, Joachim, Kienzler, Anne-Kathrin, Pan-Hammarström, Qiang, Hammarström, Lennart, Rakhmanov, Mirzokhid, Schlesier, Michael, Grimbacher, Bodo, Peter, Hans-Hartmut, Eibel, Hermann

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Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity by Willmann, Katharina L., Klaver, Stefanie, Doğu, Figen, Santos-Valente, Elisangela, Garncarz, Wojciech, Bilic, Ivan, Mace, Emily, Salzer, Elisabeth, Domínguez Conde, Cecilia, Sic, Heiko, Májek, Peter, Banerjee, Pinaki P., Vladimer, Gregory I., Haskoloğlu, Şule, Gökalp Bolkent, Musa, Küpesiz, Alphan, Condino-Neto, Antonio, Colinge, Jacques, Superti-Furga, Giulio, Pickl, Winfried F., van Zelm, Menno C., Eibel, Hermann, Orange, Jordan S., Ikincioğulları, Aydan, Boztuğ, Kaan

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Follow-up in a point-of-care diabetic retinopathy program in Pittsburgh: a non-concurrent retrospective cohort study by Bonilla-Escobar, Francisco J, Eibel, Maria Regina, Le, Laura, Gallagher, Denise S, Waxman, Evan L

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A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency by Pieper, Kathrin, PhD, Rizzi, Marta, MD, PhD, Speletas, Matthaios, MD, PhD, Smulski, Cristian R., PhD, Sic, Heiko, PhD, Kraus, Helene, MSc, Salzer, Ulrich, MD, Fiala, Gina J., MSc, Schamel, Wolfgang W., PhD, Lougaris, Vassilios, MD, Plebani, Alessandro, MD, Hammarstrom, Lennart, MD, PhD, Recher, Mike, MD, Germenis, Anastasios E., MD, PhD, Grimbacher, Bodo, MD, Warnatz, Klaus, MD, PhD, Rolink, Antonius G., PhD, Schneider, Pascal, PhD, Notarangelo, Luigi D., MD, Eibel, Hermann, PhD

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A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency by Fornes, Oriol, Jia, Alicia, Kuehn, Hye Sun, Min, Qing, Pannicke, Ulrich, Schleussner, Nikolai, Thouenon, Romane, Yu, Zhijia, de Los Angeles Astbury, María, Biggs, Catherine M, Galicchio, Miguel, Garcia-Campos, Jorge Alberto, Gismondi, Silvina, Gonzalez Villarreal, Guadalupe, Hildebrand, Kyla J, Hönig, Manfred, Hou, Jia, Moshous, Despina, Pittaluga, Stefania, Qian, Xiaowen, Rozmus, Jacob, Schulz, Ansgar S, Staines-Boone, Aidé Tamara, Sun, Bijun, Sun, Jinqiao, Uwe, Schauer, Venegas-Montoya, Edna, Wang, Wenjie, Wang, Xiaochuan, Ying, Wenjing, Zhai, Xiaowen, Zhou, Qinhua, Akalin, Altuna, André, Isabelle, Barth, Thomas F E, Baumann, Bernd, Brüstle, Anne, Burgio, Gaetan, Bustamante, Jacinta C, Casanova, Jean-Laurent, Casarotto, Marco G, Cavazzana, Marina, Chentout, Loïc, Cockburn, Ian A, Costanza, Mariantonia, Cui, Chaoqun, Daumke, Oliver, Del Bel, Kate L, Eibel, Hermann, Feng, Xiaoqian, Franke, Vedran, Gebhardt, J Christof M, Götz, Andrea, Grunwald, Stephan, Hoareau, Bénédicte, Hughes, Timothy R, Jacobsen, Eva-Maria, Janz, Martin, Jolma, Arttu, Lagresle-Peyrou, Chantal, Lai, Nannan, Li, Yaxuan, Lin, Susan, Lu, Henry Y, Lugo-Reyes, Saul O, Meng, Xin, Möller, Peter, Moreno-Corona, Nidia, Niemela, Julie E, Novakovsky, Gherman, Perez-Caraballo, Jareb J, Picard, Capucine, Poggi, Lucie, Puig-Lombardi, Maria-Emilia, Randall, Katrina L, Reisser, Anja, Schmitt, Yohann, Seneviratne, Sandali, Sharma, Mehul, Stoddard, Jennifer, Sundararaj, Srinivasan, Sutton, Harry, Tran, Linh Q, Wang, Ying, Wasserman, Wyeth W, Wen, Zichao, Winkler, Wiebke, Xiong, Ermeng, Yang, Ally W H, Yu, Meiping, Zhang, Lumin, Zhang, Hai, Zhao, Qian, Zhen, Xin, Enders, Anselm, Kracker, Sven, Martinez-Barricarte, Ruben, Mathas, Stephan, Rosenzweig, Sergio D, Schwarz, Klaus

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Recurrent respiratory tract infections (RRTI) in the elderly: A late onset mild immunodeficiency? by van de Vosse, Esther, van Ostaijen-ten Dam, Monique M, Vermaire, René, Verhard, Els M, Waaijer, Jacqueline L, Bakker, Jaap A, Bernards, Sandra T, Eibel, Hermann, van Tol, Maarten J, van Dissel, Jaap T, Haverkamp, Margje H

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Antimicrobial resistance of Streptococcus pneumoniae in Southeast Austria, 1997–2008 by Hoenigl, M, Fussi, P, Feierl, G, Wagner-Eibel, U, Leitner, E, Masoud, L, Zarfel, G, Marth, E, Grisold, A.J

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Release of endogenous anti‐inflammatory complement regulators FHL‐1 and factor H protects synovial fibroblasts during rheumatoid arthritis by FRIESE, M. A., MANUELIAN, T., JUNNIKKALA, S., HELLWAGE, J., MERI, S., PETER, H. H., GORDON, D. L., EIBEL, H., ZIPFEL, P. F.

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The Clinical and Immunological Phenotype of Human CD21 Deficiency by Thiel, J, Kimmig, L, Salzer, U, Voelxen, N, Eibel, H, Peter, H H, Grimbacher, B, Rump, JA, Schlesier, M

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