Csorba Gabriella Éva

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Name: Csorba Gabriella Éva

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Date range:

2007-2022

2022

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

Journal metrics:

Q4 Medicine (miscellaneous)

2015

Lajszné Tóth, B., Soltész, B., Gyimesi, E., Csorba, G., 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.

Journal metrics:

Q2 Immunology
Q2 Immunology and Allergy

2014

Sarkadi, A., Taskó, S., Csorba, G., 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.

Journal metrics:

Q2 Immunology
Q1 Immunology and Allergy
Soltész, B., Lajszné Tóth, B., Csorba, G., Taskó, S., Sarkadi, A., Maródi, L.: Impaired Development of IL-17-Mediated Immunity in a Patient with a Novel STAT1 Mutation.
J. Clin. Immunol. 34 (Suppl.), S175, 2014.
Lajszné Tóth, B., Soltész, B., Gyimesi, E., Csorba, G., 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.

2013

Soltész, B., Lajszné Tóth, B., Shabashova, N., Bondarenko, A., Okada, S., Cypowyj, S., Abhyankar, A., Csorba, G., Taskó, S., Sarkadi, A., Méhes, L., Rozsíval, P., Neumann, D., Chernyshova, L., Tulassay, Z., Puel, A., Casanova, J., 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.

Journal metrics:

Q1 Genetics
D1 Genetics (clinical)
Lajszné Tóth, B., Pistár, Z., Csorba, G., 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.

Journal metrics:

Q2 Hematology
Q1 Medicine (miscellaneous)

2012

Török, O., Lajszné Tóth, B., Erdős, M., Csorba, G., 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.

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., 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.

Journal metrics:

Q1 Immunology
Q2 Molecular Biology

2007

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

Journal metrics:

Q2 Hematology
Q1 Medicine (miscellaneous)

updated: 2024-11-10, 01:28

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Csorba Gabriella Éva

Csorba Gabriella Éva

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Csorba Gabriella Éva

Csorba Gabriella Éva

Publication list

SCImago quartiles ofscientific journal articles

SCImago subject areas and categories

Genre chart

Year chart

Language chart

Journals

iDEa co-authors

Other co-authors

SCImago quartiles of
scientific journal articles