Erdős Melinda

Molnár, M. J., Szlepák, T., Csürke, I., Loth, S., Káposzta, R., Erdős, M., Dezsőfi, A.: Case report: The spectrum of SMPD1 pathogenic variants in Hungary.
Front. Genet. 14, 1-6, (cikkazonosító: 1158108), 2023.

Tar, I., Szegedi, M., Krasuska-Sławińska, E., Heropolitanska-Pliszka, E., Bernatowska, E., Öncü, E., Keles, S., Guner, S. N., Reisli, I., Gesheva, N., Naumova, E., Izakovicova-Holla, L., Litzman, J., Savchak, I., Kostyuchenko, L., Erdős, M.: Intraoral and maxillofacial abnormalities in patients with autosomal dominant hyper-IgE syndrome.
Cent. Eur. J. Immunol. 48 (3), 228-236, 2023.

Erdős, M., Mironska, K., Kareva, L., Stavrik, K., Hasani, A., Lányi, Á., Kállai, J., Maródi, L.: A novel mutation in identified in a patient with autosomal recessive agammaglobulinemia: the impact of the J-Project.
Pediatr. Allergy Immunol. 33 (6), 1-7, 2022.

Abolhassani, H., Avcin, T., Bahceciler, N., Balashov, D., Bata, Z., Bataneant, M., Belevtsev, M., Bernatowska, E., Bidló, J., Blazsó, P., Boisson, B., Bolkov, M., Bondarenko, A., Boyarchuk, O., Bundschu, A., Casanova, J. L., Chernishova, L., Ciznar, P., Csürke, I., Erdős, M., Farkas, H., Fomina, D. S., Galal, N., Goda, V., Guner, S. N., Hauser, P., Ilyina, N. I., Iremadze, T., Iritsyan, S., Ismaili, J. V., Jesenak, M., Kelecic, J., Keles, S., Kindle, G., Kondratenko, I. V., Kostyuchenko, L., Kovzel, E., Kriván, G., Kuli, L. G., Kumánovics, G., Kurjane, N., Latysheva, E. A., Latysheva, T. V., Lázár, I., Markelj, G., Markovic, M., Maródi, L., Mammadova, V., Medvecz, M., Miltner, N., Mironska, K., Modell, F., Modell, V., Mosdósi, B., Mukhina, A. A., Murdjeva, M., Műzes, G., Nabieva, U., Nasrullayeva, G., Naumova, E., Nagy, K., Ónozó, B., Orozbekova, B., Pac, M., Pagava, K., Pampura, A. N., Pasic, S., Petrosyan, M., Petrovic, G., Pocek, L., Prodeus, A. P., Reisli, I., Ress, K., Rezaei, N., Rodina, Y. A., Rumyantsev, A. G., Sciuca, S., Sediva, A., Serban, M., Sharapova, S., Shcherbina, A., Sitkaustiene, B., Snimshchikova, I., Spahiu, K. S., Szolnoky, M., Szűcs, G., Toplak, N., Lajszné Tóth, B., Tsyvkina, G., Tuzankina, I., Vlasova, E., Volokha, A.: Care of patients with inborn errors of immunity in thirty J Project countries between 2004 and 2021.
Front. Immunol. 13 (13), 1-14, 2022.

Erdős, M., Tsumura, M., Kállai, J., Lányi, Á., Nyúl, Z., Balázs, G., Okada, S., Maródi, L.: Novel STAT-3 gain-of-function variant with hypogammaglobulinemia and recurrent infection phenotype.
Clin. Exp. Immunol. 205 (3), 354-362, 2021.

Erdős, M., Jakobicz, E., Soltész, B., Lajszné Tóth, B., Bata-Csörgő, Z., Maródi, L.: Recurrent, Severe Aphthous Stomatitis and Mucosal Ulcers as Primary Manifestations of a Novel STAT1 Gain-of-Function Mutation.
Front. Immunol. 11, 1-7, 2020.

Lajszné Tóth, B., Pistár, Z., Csorba, G. É., Balogh, I., Kovács, T., Erdős, M., Maródi, L.: Novel dedicator of cytokinesis 8 mutations identified by multiplex ligation-dependent probe amplification.
Eur. J. Haematol. 91 (4), 369-375, 2013.

Török, O., Lajszné Tóth, B., Erdős, M., Csorba, G. É., Gyimesi, E., Balogh, I., Tóth, Z., Maródi, L.: Molecular diagnostic challenges and complex management of consecutive twin pregnancies in a family with CD40 ligand deficiency.
Scand. J. Immunol. 75 (2), 227-230, 2012.

Maródi, L., Erdős, M.: Dectin-1 deficiency and mucocutaneous fungal infections.
N. Engl. J. Med. 362, 367-368, 2010.