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Publications in DEA:

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Date range:

2007-2022

2022

Deák, A., Koczok, K., Bessenyei, B., Szűcs, Z., Madar, L., Csorba, G. É., Orosz, O., Laki, I., Halász, A., Marsal, G., Balogh, I.: A magyar Cystás Fibrosis Regiszter genetikai revíziója.
Orv. hetil. 163 (51), 2052-2059, 2022.

doi DEA WoS Scopus

Journal metrics:

Q4 Medicine (miscellaneous)

2015

Lajszné Tóth, B., Soltész, B., Gyimesi, E., Csorba, G. É., Veres, Á., Lányi, Á., Kovács, G., Maródi, L., Erdős, M.: Severe XLP Phenotype Caused by a Novel Intronic Mutation in the SH2D1A Gene.
J. Clin. Immunol. 35 (1), 26-31, 2015.

doi DEA

Journal metrics:

Q2 Immunology

Q2 Immunology and Allergy

2014

Sarkadi, A. K., Taskó, S., Csorba, G. É., Lajszné Tóth, B., Erdős, M., Maródi, L.: Autoantibodies to IL-17A may be correlated with the severity of Mucocutaneous Candidiasis in APECED patients.
J. Clin. Immunol. 34 (2), 181-193, 2014.

doi DEA

Journal metrics:

Q2 Immunology

Q1 Immunology and Allergy

Soltész, B., Lajszné Tóth, B., Csorba, G. É., Taskó, S., Sarkadi, A. K., Maródi, L.: Impaired Development of IL-17-Mediated Immunity in a Patient with a Novel STAT1 Mutation.
J. Clin. Immunol. 34 (Suppl.), S175, 2014.

DEA

Lajszné Tóth, B., Soltész, B., Gyimesi, E., Csorba, G. É., Veres, Á., Lányi, Á., Kovács, G., Erdős, M., Maródi, L.: Molecular Characterization of a Novel Intronic Mutation in the SH2D1A Gene.
J. Clin. Immunol. 34 (Suppl.), S229, 2014.

DEA

2013

Soltész, B., Lajszné Tóth, B., Shabashova, N., Bondarenko, A., Okada, S., Cypowyj, S., Abhyankar, A., Csorba, G. É., Taskó, S., Sarkadi, A. K., Méhes, L., Rozsíval, P., Neumann, D., Chernyshova, L., Tulassay, Z., Puel, A., Casanova, J. L., Sediva, A., Litzman, J., Maródi, L.: New and recurrent gain-of-function STAT1 mutations in patients with chronic mucocutaneous candidiasis from Eastern and Central Europe.
J. Med. Genet. 50 (9), 567-578, 2013.

doi DEA

Journal metrics:

Q1 Genetics

D1 Genetics (clinical)

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.

doi DEA

Journal metrics:

Q2 Hematology

Q1 Medicine (miscellaneous)

2012

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.

doi DEA

Journal metrics:

Q3 Immunology

Q1 Medicine (miscellaneous)

2008

Jiao, H., Lajszné Tóth, B., Erdős, M., Fransson, I., Rákóczi, É., Balogh, I., Magyarics, Z., Dérfalvy, B., Csorba, G. É., Szaflarska, A., Megarbane, A., Akatcherian, C., Dbaibo, G., Rajnavölgyi, É., Hammarström, L., Kere, J., Lefranc, G., Maródi, L.: Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups.
Mol. Immunol. 46 (1), 202-206, 2008.

doi DEA

Journal metrics:

Q1 Immunology

Q2 Molecular Biology

2007

10.

Alapi, K., Erdős, M., Csorba, G. É., Maródi, L.: Recurrent CXCR4 sequence variation in a girl with incomplete WHIM syndrome.
Eur. J.Haemat. 78 (1), 86-88, 2007.

doi DEA

Journal metrics:

Q2 Hematology

Q1 Medicine (miscellaneous)