Nijmegen Breakage Syndrome: Clinical and Immunological Features, Long-Term Outcome and Treatment Options – a Retrospective Analysis by Wolska-Kuśnierz, Beata, Gregorek, Hanna, Chrzanowska, Krystyna, Piątosa, Barbara, Pietrucha, Barbara, Heropolitańska-Pliszka, Edyta, Pac, Małgorzata, Klaudel-Dreszler, Maja, Kostyuchenko, Larysa, Pasic, Srdjan, Marodi, Laszlo, Belohradsky, Bernd H., Čižnár, Peter, Shcherbina, Anna, Kilic, Sara Sebnem, Baumann, Ulrich, Seidel, Markus G., Gennery, Andrew R., Syczewska, Małgorzata, Mikołuć, Bożena, Kałwak, Krzysztof, Styczyński, Jan, Pieczonka, Anna, Drabko, Katarzyna, Wakulińska, Anna, Gathmann, Benjamin, Albert, Michael H., Skarżyńska, Urszula, Bernatowska, Ewa

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fSCIG 10% in pediatric primary immunodeficiency diseases: a European post-authorization safety study by Čižnár, Peter, Roderick, Marion, Schneiderova, Helen, Jeseňák, Miloš, Kriván, Gergely, Brodszki, Nicholas, Jolles, Stephen, Atisso, Charles, Fielhauer, Katharina, Saeed-Khawaja, Shumyla, McCoy, Barbara, Yel, Leman

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Dynamics of allergy development during the first 5 years of life by Vrbova, Marketa, Dorociakova, Petra, Vyskovsky, Roman, Palkovicova Murinova, Lubica, Ciznar, Peter, Rausova, Katarina, McNabb, Scott J. N., Reichrtova, Eva, Budinska, Eva, Thon, Vojtech

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Immunologic Phenotype of a Child With the MEHMO Syndrome by TROCHANOVÁ, I, STANÍKOVÁ, D, ŠKOPKOVÁ, M, HAŠTOVÁ, K, GAŠPERÍKOVÁ, D, STANÍK, J, ČIŽNÁR, P

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Evaluating the Replacement of Galvanic Cr Coatings by Trebuňa, Peter, Kottfer, Daniel, Pekarčíková, Miriam, Petriková, Andrea, Popovič, Radko, Rehák, František, Čižnár, Peter

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THE EFFECT OF PRESSURE, BIAS VOLTAGE AND ANNEALING TEMPERATURE ON N₂ AND N₂+SiH₄ DOPED WC/C DC MAGNETRON SPUTTERED LAYERS by Hornak, Peter

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The importance of defining the age-specific TREC/KREC levels for detection of various inborn errors of immunity in pediatric and adult patients by Medova, Veronika, Hulinkova, Ivana, Laiferova, Nikoleta, Urdova, Veronika, Ciznar, Peter, Dolnikova, Dana, Krasnanova, Veronika, Fabri, Oksana, Ficek, Andrej, Soltysova, Andrea

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Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome by Béziat, Vivien, Tavernier, Simon J, Chen, Yin-Huai, Ma, Cindy S, Materna, Marie, Laurence, Arian, Staal, Jens, Aschenbrenner, Dominik, Roels, Lisa, Worley, Lisa, Claes, Kathleen, Gartner, Lisa, Kohn, Lisa A, De Bruyne, Marieke, Schmitz-Abe, Klaus, Charbonnier, Louis-Marie, Keles, Sevgi, Nammour, Justine, Vladikine, Natasha, Maglorius Renkilaraj, Majistor Raj Luxman, Seeleuthner, Yoann, Migaud, Mélanie, Rosain, Jérémie, Jeljeli, Mohamed, Boisson, Bertrand, Van Braeckel, Eva, Rosenfeld, Jill A, Dai, Hongzheng, Burrage, Lindsay C, Murdock, David R, Lambrecht, Bart N, Avettand-Fenoel, Véronique, Vogel, Tiphanie P, Esther, Charles R, Haskologlu, Sule, Dogu, Figen, Ciznar, Peter, Boutboul, David, Ouachée-Chardin, Marie, Amourette, Jean, Lebras, Marie-Noëlle, Gauvain, Clément, Tcherakian, Colas, Ikinciogullari, Aydan, Beyaert, Rudi, Abel, Laurent, Milner, Joshua D, Grimbacher, Bodo, Couderc, Louis-Jean, Butte, Manish J, Freeman, Alexandra F, Catherinot, Émilie, Fieschi, Claire, Chatila, Talal A, Tangye, Stuart G, Uhlig, Holm H, Haerynck, Filomeen, Casanova, Jean-Laurent, Puel, Anne

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Biallelic Cys141Tyr variant of SEL1L is associated with neurodevelopmental disorders, agammaglobulinemia, and premature death by Weis, Denisa, Lin, Liangguang L, Wang, Huilun H, Li, Zexin Jason, Kusikova, Katarina, Ciznar, Peter, Wolf, Hermann M, Leiss-Piller, Alexander, Wang, Zhihong, Wei, Xiaoqiong, Weis, Serge, Skalicka, Katarina, Hrckova, Gabriela, Danisovic, Lubos, Soltysova, Andrea, Yang, Tingxuan T, Feichtinger, René Günther, Mayr, Johannes A, Qi, Ling

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Activated phosphoinositide 3-kinase d syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity by Maccari, ME, Wolkewitz, M, Schwab, C, Lorenzini, T, Leiding, JW, Aladjdi, N, Abolhassani, H, Abou-Chahla, W, Aiuti, A, Azarnoush, S

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Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases by Conti, Francesca, MD, PhD, Lugo-Reyes, Saul Oswaldo, MD, Blancas Galicia, Lizbeth, MD, He, Jianxin, MD, Aksu, Güzide, MD, Borges de Oliveira, Edgar, PhD, Deswarte, Caroline, MSc, Hubeau, Marjorie, PhD, Karaca, Neslihan, MD, de Suremain, Maylis, AS, Guérin, Antoine, MSc, Baba, Laila Ait, PhD, Prando, Carolina, MD, PhD, Guerrero, Gloria G., PhD, Emiroglu, Melike, MD, Öz, Fatma Nur, MD, Yamazaki Nakashimada, Marco Antonio, MD, Gonzalez Serrano, Edith, MD, Espinosa, Sara, MD, PhD, Barlan, Isil, MD, Pérez, Nestor, MD, PhD, Regairaz, Lorena, MD, Guidos Morales, Héctor Eduardo, MD, Bezrodnik, Liliana, MD, Di Giovanni, Daniela, MD, Dbaibo, Ghassan, MD, Ailal, Fatima, MD, Galicchio, Miguel, MD, Oleastro, Matias, MD, Chemli, Jalel, MD, Danielian, Silvia, PhD, Perez, Laura, BSc, Ortega, Maria Claudia, MD, Soto Lavin, Susana, MD, PhD, Hertecant, Joseph, MD, Anal, Ozden, MD, Kechout, Nadia, MD, Al-Idrissi, Eman, MD, ElGhazali, Gehad, MD, PhD, Bondarenko, Anastasia, MD, Chernyshova, Liudmyla, MD, Ciznar, Peter, MD, Herbigneaux, Rose-Marie, MD, Diabate, Aminata, AS, Ndaga, Stéphanie, AS, Konte, Barik, AS, Czarna, Ambre, AS, Migaud, Mélanie, AS, Pedraza-Sánchez, Sigifredo, PhD, Zaidi, Mussaret Bano, MD, Msc, Vogt, Guillaume, PhD, Blanche, Stéphane, MD, Benmustapha, Imen, MD, Mansouri, Davood, MD, Abel, Laurent, MD, PhD, Boisson-Dupuis, Stéphanie, PhD, Mahlaoui, Nizar, MD, MSc, MPH, Bousfiha, Ahmed Aziz, MD, Picard, Capucine, MD, PhD, Barbouche, Ridha, MD, PhD, Al-Muhsen, Saleh, MD, Espinosa-Rosales, Francisco J., MD, Kütükçüler, Necil, MD, Condino-Neto, Antonio, MD, PhD, Casanova, Jean-Laurent, MD, PhD, Bustamante, Jacinta, MD, PhD

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Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival by Vallée, Tanja C., Glasmacher, Jannik S., Buchner, Hannes, Arkwright, Peter D., Behrends, Uta, Bondarenko, Anastasia, Browning, Michael J., Buchbinder, David, Cattoni, Alessandro, Chernyshova, Liudmyla, Ciznar, Peter, Cole, Theresa, Czogała, Wojciech, Dueckers, Gregor, Edgar, John David M., Erbey, Fatih, Fasth, Anders, Ferrua, Francesca, Formankova, Renata, Gambineri, Eleonora, Gennery, Andrew R., Goldman, Frederick D., Gonzalez-Granado, Luis I., Heilmann, Carsten, Heiskanen-Kosma, Tarja, Juntti, Hanna, Kainulainen, Leena, Kanegane, Hirokazu, Karaca, Neslihan E., Kilic, Sara S., Klein, Christoph, Kołtan, Sylwia, Kondratenko, Irina, Meyts, Isabelle, Nasrullayeva, Gulnara M., Notarangelo, Lucia D., Pasic, Srdjan, Pellier, Isabelle, Pignata, Claudio, Misbah, Siraj, Schulz, Ansgar, Segundo, Gesmar R., Shcherbina, Anna, Slatter, Mary, Sokolic, Robert, Soler-Palacin, Pere, Stepensky, Polina, van Montfrans, Joris M., Ryhänen, Samppa, Wolska-Kuśnierz, Beata, Ziegler, John B., Zhao, Xiaodong, Aiuti, Alessandro, Ochs, Hans D., Albert, Michael H.

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Validation of Risk Factors for Early Mortality in Cartilage-Hair Hypoplasia by Vakkilainen, Svetlana, Ahonen, Kira, Mäkitie, Outi

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Wiskott-Aldrich Syndrome: A study on 577 patients defining the genotype as a predictive biomarker for disease severity by Vallée, Tanja C, Glasmacher, Jannik S, Buchner, Hannes, Arkwright, Peter D, Behrends, Uta, Bondarenko, Anastasia, Browning, Michael J, Buchbinder, David K, Cattoni, Alessandro, Chernyshova, Liudmyla, Ciznar, Peter, Cole, Theresa, Czogala, Wojciech, Dueckers, Gregor, Edgar, John David M, Erbey, Fatih, Fasth, Anders, Ferrua, Francesca, Formankova, Renata, Gambineri, Eleonora, Gennery, Andrew R, Goldman, Frederick D, Gonzalez-Granado, Luis Ignacio, Heilmann, Carsten, Heiskanen-Kosma, Tarja, Juntti, Hanna, Kainulainen, Leena, Kanegane, Hirokazu, Karaca, Neslihan E., Sebnem Kilic, Sara, Klein, Christoph, Koltan, Sylwia, Kondratenko, Irina, Meyts, Isabelle, Nasrullayeva, Gulnara M, Notarangelo, Lucia Dora, Pasic, Srdjan, Pellier, Isabelle, Pignata, Claudio, Misbah, Siraj Ahmed, Schulz, Ansgar S, Segundo, Gesmar RS, Shcherbina, Anna, Slatter, Mary A, Sokolic, Robert, Soler-Palacin, Pere, Stepensky, Polina, van Montfrans, Joris M., Ryhänen, Samppa, Wolska-Kuśnierz, Beata, Ziegler, John B, Zhao, Xiaodong, Aiuti, Alessandro, Ochs, Hans D, Albert, Michael H

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Environmental and dietary risk factors for infantile atopic eczema among a Slovak birth cohort by Dunlop, Anne L., Reichrtova, Eva, Palcovicova, Luba, Ciznar, Peter, Adamcakova-Dodd, Andrea, Smith, S. J., McNabb, Scott J. N.

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Autoantibodies against type I IFNs in humans with alternative NF- K B pathway deficiency by Le Voyer, Tom, Liu, Xian, Gervais, Adrian, Rosain, Jeremie, Lorenzo, Malena Perez, Zhang, Peng, Bizien, Lucy, Charuel, Jean-Luc, Philippot, Quentin, Renkilaraj, Majistor Raj Luxman Maglorius, Ogishi, Masato, Migaud, Melanie, Rozenberg, Flore, Momenilandi, Mana, Riller, Quentin, Imberti, Luisa, Mueller, Gabriele, Keller, Baerbel, Gallego, William Alexander Franco, Rubin, Tamar, Emiroglu, Melike, Parvaneh, Nima, Eriksson, Daniel, Aranda-Guillen, Maribel, Berrios, David I., Vong, Linda, Mustillo, Peter, Raedler, Johannes, Bohlen, Jonathan, Astudillo, Camila, Winter, Sarah, DeRisi, Joseph L., Yu, David, Feng, Yi, Guichard, Audrey, Zhang, Yu, Rosen, Lindsey B., Holland, Steve M., Bosticardo, Marita, Kenney, Heather, Castagnoli, Riccardo, Slade, Charlotte A., Boztug, Kaan, Mahlaoui, Nizar, Abraham, Roshini S., Lougaris, Vassilios, Hauck, Fabian, Sediva, Anna, Sogkas, Georgios, Poli, M. Cecilia, Slatter, Mary A., Palterer, Boaz, Keller, Michael D., Pinzon-Charry, Alberto, Sullivan, Anna, Wong, Melanie, Ma, Cindy, Grombirikova, Hana, Dalal, Ilan, Aladjidi, Nathalie, Lazaro, Estibaliz, Keles, Sevgi, Malphettes, Marion, Maccari, Maria Elena, Meinhardt, Andrea, Shahrooei, Mohammad, Celmeli, Fatih, Frosk, Patrick, Goodnow, Christopher C., Gray, Paul E., Belot, Alexandre, Kuehn, Hye Sun, Rosenzweig, Sergio D., Miyara, Makoto, Servettaz, Amelie, Barlogis, Vincent, Le Guenno, Guillaume, Herrmann, Vera-Maria, Kuijpers, Taco, Schuetz, Catharina, Cunningham-Rundles, Charlotte, Rieux-Laucat, Frederic, Tangye, Stuart G., Warnatz, Klaus, Grimbacher, Bodo, Fieschi, Claire, Berteloot, Laureline, Bryant, Vanessa L., Assant, Sophie Trouillet, Su, Helen, Neven, Benedicte, Zhang, Qian, Boisson, Bertrand, Jouanguy, Emmanuelle, Bastard, Paul, Landegren, Nils, Notarangelo, Luigi D., Anderson, Mark S., Casanova, Jean-Laurent, Puel, Anne

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Simple Measurement of IgA Predicts Immunity and Mortality in Ataxia-Telangiectasia by Zielen, Stefan, Duecker, Ruth Pia, Woelke, Sandra, Donath, Helena, Bakhtiar, Sharhzad, Buecker, Aileen, Kreyenberg, Hermann, Huenecke, Sabine, Bader, Peter, Mahlaoui, Nizar, Ehl, Stephan, El-Helou, Sabine M., Pietrucha, Barbara, Plebani, Alessandro, van der Flier, Michiel, van Aerde, Koen, Kilic, Sara S., Reda, Shereen M., Kostyuchenko, Larysa, McDermott, Elizabeth, Galal, Nermeen, Pignata, Claudio, Pérez, Juan Luis Santos, Laws, Hans-Juergen, Niehues, Tim, Kutukculer, Necil, Seidel, Markus G., Marques, Laura, Ciznar, Peter, Edgar, John David M., Soler-Palacín, Pere, von Bernuth, Horst, Krueger, Renate, Meyts, Isabelle, Baumann, Ulrich, Kanariou, Maria, Grimbacher, Bodo, Hauck, Fabian, Graf, Dagmar, Granado, Luis Ignacio Gonzalez, Prader, Seraina, Reisli, Ismail, Slatter, Mary, Rodríguez-Gallego, Carlos, Arkwright, Peter D., Bethune, Claire, Deripapa, Elena, Sharapova, Svetlana O., Lehmberg, Kai, Davies, E. Graham, Schuetz, Catharina, Kindle, Gerhard, Schubert, Ralf

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Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations by Giardino, Giuliana, Sharapova, Svetlana O., Ciznar, Peter, Dhalla, Fatima, Maragliano, Luca, Radha Rama Devi, Akella, Islamoglu, Candan, Ikinciogullari, Aydan, Haskologlu, Sule, Dogu, Figen, Hanna-Wakim, Rima, Dbaibo, Ghassan, Chou, Janet, Cirillo, Emilia, Borzacchiello, Carla, Kreins, Alexandra Y., Worth, Austen, Rota, Ioanna A., Marques, José G., Sayitoglu, Muge, Firtina, Sinem, Mahdi, Moaffaq, Geha, Raif, Neven, Bénédicte, Sousa, Ana E., Benfenati, Fabio, Hollander, Georg A., Davies, E. Graham, Pignata, Claudio

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Terminal 14q32.33 deletion as a novel cause of agammaglobulinemia by Geier, Christoph B., Piller, Alexander, Eibl, Martha M., Ciznar, Peter, Ilencikova, Denisa, Wolf, Hermann M.

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The European internet‐based patient and research database for primary immunodeficiencies: update 2011 by Gathmann, B., Binder, N., Ehl, S., Kindle, G.

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