 |
|
| Personal data sheet |
 Print previewpersonal data approved: 2024. I. 12. | Publications |
2023
 from data base, 2024. I. 12. |
Hurler Lisa, Szilágyi Ágnes, Mescia Federica, Bergamaschi Laura, Mező Blanka, Sinkovits György, Réti Marienn, Müller Veronika, Iványi Zsolt, Gál János, Gopcsa László, Reményi Péter, Szathmáry Beáta, Lakatos Botond, Szlávik János, Bobek Ilona, Prohászka Zita Z., Förhécz Zsolt, Csuka Dorottya, Kajdácsi Erika, Cervenak László, Kiszel Petra, Masszi Tamás, Vályi-Nagy István, Würzner Reinhard, Lyons Paul A., Toonen Erik J. M., Prohászka Zoltán: Complement lectin pathway activation is associated with COVID-19 disease severity, independent of MBL2 genotype subgroups, FRONTIERS IN IMMUNOLOGY 14: 1162171
type of document:
number of independent citations: 1
language: English
URL |
2022
from data base, 2024. I. 12. |
Szilágyi Á., Csuka D., Geier C.B., Prohászka Z.: Complement Genetics for the Practicing Allergist Immunologist: Focus on Complement Deficiencies, JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY: IN PRACTICE 10: (7) pp. 1703-1711.
type of document: Journal paper/Review paper
number of independent citations: 1
language: English
URL |
2022
from data base, 2024. I. 12. |
Szabó Edina, Csuka Dorottya, Andrási Noémi, Varga Lilian, Farkas Henriette, Szilágyi Ágnes: Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema, FRONTIERS IN ALLERGY 3: 836465
type of document: Journal paper/Article
number of independent citations: 3
language: English
URL |
2022
from data base, 2024. I. 12. |
Rysava R., Peiskerova M., Tesar V., Benes J., Kment M., Szilágyi Á., Csuka D., Prohászka Z.: Atypical hemolytic uremic syndrome triggered by mRNA vaccination against SARS-CoV-2: Case report, FRONTIERS IN IMMUNOLOGY 13: 1001366
type of document: Journal paper/Article
number of independent citations: 8
language: English
URL |
2020
from data base, 2024. I. 12. |
Germenis Anastasios E, Margaglione Maurizio, Pesquero João Bosco, Farkas Henriette, Cichon Sven, Csuka Dorottya, Lera Alberto López, Rijavec Matija, Jolles Stephen, Szilagyi Agnes, Trascasa Margarita López, Veronez Camila Lopes, Drouet Christian, Zamanakou Maria, Andrejevic Sladjana, Aygören-Pürsün Emel, Bara Noemi-Anna, Bernstein Jonathan, Bork Konrad, Bouillet Laurence, Bova Maria, Boysen Henrik Halle, Bygum Anette, Caballero Teresa, Castaldo Anthony, Christiansen Sandra, Cicardi Marco, Fabiani Jose, Katelaris Connie, Dewald Georg, Gökmen Nihal M, Gonzalez-Quevedo Maria Teresa, Gooi Jimmy, Grivcheva-Panovska Vesna, Grumach Anete, Hakl Roman, Hardy Gaelle, Jesenak Milos, Kaplan Allen, Kirschfink Michael, Köhalmi Kinga Viktoria, Leibovich Iris, Longhurst Hilary J, Lumry William, Magerl Markus, Saguer Inmaculada Martinez, Nagy Imola Beatrix, Nieto Sandra, Nordenfelt Patrik, Porębski Grzegorz, Psarros Fotis, Reshef Avner, Riedl Marc A, Sheikh Farrukh, Peter Spath, Speletas Matthaios, Staevska Maria, Stobiecki Marcin, Triggiani Massimo, Veszeli Nora, Waserman Susan, Weber Christina, Wuillemin Walter, Zuraw Bruce: International Consensus on the Use of Genetics in the Management of Hereditary Angioedema., JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY: IN PRACTICE 8: (3) pp. 901-911.
type of document:
number of independent citations: 13
language: English
URL |
2016
from data base, 2024. I. 12. |
Szarvas Nóra, Szilágyi Ágnes, Csuka Dorottya, Takács Beáta, Rusai Krisztina, Müller Thomas, Arbeiter Klaus, Réti Marienn, Haris Ágnes, Wagner László, Török Szilárd, Kelen Kata, Szabó Attila J, Reusz György S, Morgan B Paul, Prohászka Zoltán: Genetic analysis and functional characterization of novel mutations in a series of patients with atypical hemolytic uremic syndrome, MOLECULAR IMMUNOLOGY 71: pp. 10-22.
type of document: Journal paper/Article
number of independent citations: 20
language: English
URL |
2014
from data base, 2024. I. 12. |
Kronbichler A, Frank R, Kirschfink M, Szilágyi Á, Csuka D, Prohászka Z, Schratzberger P, Lhotta K, Mayer G: Efficacy of eculizumab in a patient with immunoadsorption- dependent catastrophic antiphospholipid syndrome: A case report, MEDICINE 93: (26) p. e143.
type of document:
number of independent citations: 81
language: English
URL |
2013
from data base, 2024. I. 12. |
Bors A, Csuka D, Varga L, Farkas H, Tordai A, Fust G, Szilagyi A: Less severe clinical manifestations in patients with hereditary angioedema with missense C1INH gene mutations., JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 131: (6) pp. 1708-1711.
type of document:
number of independent citations: 19
language: English
URL |
2013
from data base, 2024. I. 12. |
Szilágyi Á, Kiss N, Bereczki Cs, Tálosi Gy, Rácz K, Túri S, Györke Zs, Simon E, Horváth E, Kelen K, Reusz Gy, Szabó AJ, Tulassay T, Prohászka Z: The role of complement in Streptococcus pneumoniae-associated haemolytic uraemic syndrome, NEPHROLOGY DIALYSIS TRANSPLANTATION 28: (9) pp. 2237-2245.
type of document: Journal paper/Article
number of independent citations: 63
language: English
URL |
2013
from data base, 2024. I. 12. |
Kiss N, Barabas E, Varnai K, Halasz A, Varga LA, Prohaszka Z, Farkas H, Szilagyi A: Novel duplication in the F12 gene in a patient with recurrent angioedema., CLINICAL IMMUNOLOGY 149: (1) pp. 142-145.
type of document:
number of independent citations: 59
language: English
URL |
| | Number of independent citations to these publications: | 268 |
|
|
|
|
|
Login
