Intraoral and maxillofacial abnormalities in patients with autosomal dominant hyper-IgE syndrome von Tar, Ildikó, Szegedi, Márta, Krasuska-Sławińska, Ewa, Heropolitańska-Pliszka, Edyta, Bernatowska, Ewa A., Öncü, Elif, Keles, Sevgi, Guner, Sukru N., Reisli, Ismail, Gesheva, Nevena, Naumova, Elissaveta, Izakovicova-Holla, Lydie, Litzman, Jiri, Savchak, Igor, Kostyuchenko, Larysa, Erdős, Melinda

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Case Report: Association between cyclic neutropenia and SRP54 deficiency von Erdős, Melinda, Boyarchuk, Oksana, Maródi, László

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Inherited TOP2B Mutation: Possible Confirmation of Mutational Hotspots in the TOPRIM Domain von Erdős, Melinda, Lányi, Árpád, Balázs, György, Casanova, Jean-Laurent, Boisson, Bertrand, Maródi, László

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Persistently Increased Anti-cytokine Antibodies Without Clinical Disease in a Boy with APS1 Genotype von Erdős, Melinda, Kärner, Jaanika, Ranki, Annamari, Kisand, Kai, Maródi, László

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Case report: The spectrum of SMPD1 pathogenic variants in Hungary von Molnar, Maria Judit, Szlepak, Tamas, Csürke, Ildikó, Loth, Szendile, Káposzta, Rita, Erdős, Melinda, Dezsőfi, Antal

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Recurrent, Severe Aphthous Stomatitis and Mucosal Ulcers as Primary Manifestations of a Novel STAT1 Gain-of-Function Mutation von Erdos, Melinda, Jakobicz, Eszter, Soltesz, Beata, Toth, Beata, Bata-Csorgo, Zsuzsanna, Marodi, Laszlo

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IRAK4 and NEMO mutations in otherwise healthy children with recurrent invasive pneumococcal disease von Ku, Cheng-Lung, Picard, Capucine, Erdös, Melinda, Jeurissen, Axel, Bustamante, Jacinta, Puel, Anne, von Bernuth, Horst, Filipe-Santos, Orchidée, Chang, Huey-Hsuan, Lawrence, Tatiana, Raes, Marc, Maródi, László, Bossuyt, Xavier, Casanova, Jean-Laurent

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Novel STAT‐3 gain‐of‐function variant with hypogammaglobulinemia and recurrent infection phenotype von Erdős, Melinda, Tsumura, Miyuki, Kállai, Judit, Lányi, Árpád, Nyul, Zoltán, Balázs, György, Okada, Satoshi, Maródi, László

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A novel mutation in SLC39A7 identified in a patient with autosomal recessive agammaglobulinemia: The impact of the J Project von Erdős, Melinda, Mironska, Kristina, Kareva, Lidia, Stavric, Katarina, Hasani, Arijeta, Lányi, Árpád, Kállai, Judit, Maródi, László

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Autoantibodies to IL-17A may be Correlated with the Severity of Mucocutaneous Candidiasis in APECED Patients von Sarkadi, Adrien Katalin, Taskó, Szilvia, Csorba, Gabriella, Tóth, Beáta, Erdős, Melinda, Maródi, László

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Characterization of a new disease-causing mutation of SH2D1A in a family with X-linked lymphoproliferative disease von Erdõs, Melinda, Uzvölgyi, Éva, Nemes, Zoltán, Török, Olga, Rákóczi, Éva, Went-Sümegi, Nils, Sümegi, János, Maródi, László

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Novel sequence variation of AIRE and detection of interferon-ω antibodies in early infancy von Tóth, Beáta, Wolff, Anette S. B., Halász, Zita, Tar, Attila, Szüts, Péter, Ilyés, István, Erdős, Melinda, Szegedi, Gyula, Husebye, Eystein S., Zeher, Margit, Maródi, László

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Genetic characteristics of eighty-seven patients with the Wiskott–Aldrich syndrome von Gulácsy, Vera, Freiberger, Tomas, Shcherbina, Anna, Pac, Malgorzata, Chernyshova, Liudmyla, Avcin, Tadej, Kondratenko, Irina, Kostyuchenko, Larysa, Prokofjeva, Tatjana, Pasic, Srdjan, Bernatowska, Ewa, Kutukculer, Necil, Rascon, Jelena, Iagaru, Nicolae, Mazza, Cinzia, Tóth, Beáta, Erdős, Melinda, van der Burg, Mirjam, Maródi, László

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Dectin-1 Deficiency and Mucocutaneous Fungal Infections von Maródi, László, Erdös, Melinda, Ferwerda, Gerben, Kullberg, Bart Jan, Netea, Mihai G

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Neuroendocrine carcinoma associated with X-linked hyper-immunoglobulin M syndrome: Report of four cases and review of the literature von Erdős, Melinda, Garami, Miklós, Rákóczi, Éva, Zalatnai, Attila, Steinbach, Daniel, Baumann, Ulrich, Kropshofer, Gabrielle, Tóth, Beáta, Maródi, László

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Novel dedicator of cytokinesis 8 mutations identified by multiplex ligation-dependent probe amplification von Tóth, Beáta, Pistár, Zsuzsanna, Csorba, Gabriella, Balogh, István, Kovács, Tímea, Erdős, Melinda, Maródi, László

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Successful umbilical cord blood stem cell transplantation in a child with WHIM syndrome von Kriván, Gergely, Erdős, Melinda, Kállay, Krisztián, Benyó, Gábor, Tóth, Ágnes, Sinkó, János, Goda, Vera, Tóth, Beáta, Maródi, László

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Hepatic abscess as the single manifestation of X-linked chronic granulomatous disease von Székely, Annamária, Péter Jr, Mózes, Erdős, Melinda, Maródi, László

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Recurrent infection with genetically identical pneumococcal isolates in a patient with interleukin-1 receptor-associated kinase-4 deficiency von Szabo, Judit, Dobay, Orsolya, Erdos, Melinda, Borbely, Agnes, Rozgonyi, Ferenc, Marodi, Laszlo

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Recurrent CXCR4 sequence variation in a girl with WHIM syndrome von Alapi, Krisztina, Erdős, Melinda, Kovács, Gabriella, Maródi, László

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