Editorial: Screening for Primary Immunodeficiency Disorders (PIDDs) in Neonates von Hossny, Elham, Condino-Neto, Antonio, Hammarstrom, Lennart, Walter, Jolan Eszter

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Case Report: A Novel Pathogenic Missense Mutation in FAS: A Multi-Generational Case Series of Autoimmune Lymphoproliferative Syndrome von Gaefke, Claudia L., Metts, Jonathan, Imanirad, Donya, Nieves, Daime, Terranova, Paola, Dell'Orso, Gianluca, Gambineri, Eleonora, Miano, Maurizio, Lockey, Richard F., Walter, Jolan Eszter, Westermann-Clark, Emma

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SCID and Other Inborn Errors of Immunity with Low TRECs — the Brazilian Experience von Barreiros, Lucila Akune, Sousa, Jusley Lira, Geier, Christoph, Leiss-Piller, Alexander, Kanegae, Marilia Pylles Patto, França, Tábata Takahashi, Boisson, Bertrand, Lima, Alessandra Miramontes, Costa-Carvalho, Beatriz Tavares, Aranda, Carolina Sanchez, de Moraes-Pinto, Maria Isabel, Segundo, Gesmar Rodrigues Silva, Ferreira, Janaira Fernandes Severo, Tavares, Fabíola Scancetti, Guimarães, Flávia Alice Timburiba de Medeiros, Toledo, Eliana Cristina, da Matta Ain, Ana Carolina, Moreira, Iramirton Figueirêdo, Soldatelli, Gustavo, Grumach, Anete Sevciovic, de Barros Dorna, Mayra, Weber, Cristina Worm, Di Gesu, Regina Sumiko Watanabe, Dantas, Vera Maria, Fernandes, Fátima Rodrigues, Torgerson, Troy Robert, Ochs, Hans Dietrich, Bustamante, Jacinta, Walter, Jolan Eszter, Condino-Neto, Antonio

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Hypomorphic RAG deficiency: impact of disease burden on survival and thymic recovery argues for early diagnosis and HSCT von Schuetz, Catharina, Gerke, Julia, Ege, Markus Johannes, Walter, Jolan Eszter, Kusters, Maaike, Worth, Austen JJ, Kanakry, Jennifer A, Dimitrova, Dimana, Wolska-Kusnierz, Beata, Chen, Karin, Unal, Ekrem, Karakukcu, Musa, Pashchenko, Olga, Leiding, Jennifer W, Kawai, Tomoki, Amrolia, Persis Jal, Berghuis, Dagmar, Buechner, Jochen, Buchbinder, David, Cowan, Morton J, Gennery, Andrew R, Güngör, Tayfun, Heimall, Jennifer R, Miano, Maurizio, Meyts, Isabelle, Morris, Emma C, Rivière, Jacques G, Sharapova, Svetlana O, Shaw, Peter J, Slatter, Mary A, Honig, Manfred, Veys, Paul, Fischer, Alain, Cavazzana, Marina, Moshous, Despina, Schulz, Ansgar S, Albert, Michael H, Puck, Jennifer M, Lankester, Arjan C, Notarangelo, Luigi D, Neven, Bénédicte

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Case Report: A Novel Pathogenic Missense Mutation in FAS: A Multi-Generational Case Series of Autoimmune Lymphoproliferative Syndrome von Gaefke, Claudia L, Metts, Jonathan, Imanirad, Donya, Nieves, Daime, Terranova, Paola, Dell'Orso, Gianluca, Gambineri, Eleonora, Miano, Maurizio, Lockey, Richard F, Walter, Jolan Eszter, Westermann-Clark, Emma

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