• 5018 Citations
  • 35 h-Index
19972020

Research output per year

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Research Output

Article

Abdominal symptoms of hereditary angioedema and early weaning

Kelemen, Z., Visy, B., Csuka, D., Czaller, I., Füst, G. & Farkas, H., szept. 1 2010, In : European Journal of Clinical Nutrition. 64, 9, p. 1025-1027 3 p.

Research output: Article

1 Citation (Scopus)

Acquired angioedema associated with chronic hepatitis C

Farkas, H., Csepregi, A., Nemesánszky, E., Pár, A., Gyeney, L., Varga, L. & Füst, G., jan. 1 1999, In : Journal of Allergy and Clinical Immunology. 103, 4, p. 711-712 2 p.

Research output: Article

18 Citations (Scopus)
8 Citations (Scopus)

Activation of the ficolin-lectin pathway during attacks of hereditary angioedema

Csuka, D., Munthe-Fog, L., Hein, E., Zotter, Z., Prohászka, Z., Farkas, H., Varga, L. & Garred, P., dec. 1 2014, In : Journal of Allergy and Clinical Immunology. 134, 6, p. 1388-1393.e1

Research output: Article

10 Citations (Scopus)
9 Citations (Scopus)
68 Citations (Scopus)
38 Citations (Scopus)
14 Citations (Scopus)

A novel assay to diagnose hereditary angioedema utilizing inhibition of bradykinin-forming enzymes

Joseph, K., Bains, S., Tholanikunnel, B. G., Bygum, A., Aabom, A., Koch, C., Farkas, H., Varga, L., Ghebrehiwet, B. & Kaplan, A. P., jan. 1 2015, In : Allergy: European Journal of Allergy and Clinical Immunology. 70, 1, p. 115-119 5 p.

Research output: Article

14 Citations (Scopus)

A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency

Vatsiou, S., Zamanakou, M., Loules, G., Psarros, F., Parsopoulou, F., Csuka, D., Valerieva, A., Staevska, M., Porebski, G., Obtulowicz, K., Magerl, M., Maurer, M., Speletas, M., Farkas, H. & Germenis, A. E., jan. 1 2020, (Accepted/In press) In : Allergology International.

Research output: Article

Open Access
4 Citations (Scopus)

Antibody-mediated inhibition of FXIIa blocks downstream bradykinin generation

Cao, H., Biondo, M., Lioe, H., Busfield, S., Rayzman, V., Nieswandt, B., Bork, K., Harrison, L. C., Auyeung, P., Farkas, H., Csuka, D., Pelzing, M., Dower, S., Wilson, M. J., Nash, A., Nolte, M. W. & Panousis, C., okt. 2018, In : Journal of Allergy and Clinical Immunology. 142, 4, p. 1355-1358 4 p.

Research output: Article

5 Citations (Scopus)
7 Citations (Scopus)

Assessment of inhibitory antibodies in patients with hereditary angioedema treated with plasma-derived C1 inhibitor

Farkas, H., Varga, L., Moldovan, D., Obtulowicz, K., Shirov, T., Machnig, T., Feuersenger, H., Edelman, J., Williams-Herman, D. & Rojavin, M., nov. 1 2016, In : Annals of Allergy, Asthma and Immunology. 117, 5, p. 508-513 6 p.

Research output: Article

5 Citations (Scopus)
6 Citations (Scopus)
2 Citations (Scopus)

Bacteriuria increases the risk of edematous attacks in hereditary angioedema with C1-inhibitor deficiency

Zotter, Z., Veszeli, N., Kőhalmi, K. V., Varga, L., Imreh, Kovács, G., Nallbani, M. & Farkas, H., dec. 1 2016, In : Allergy: European Journal of Allergy and Clinical Immunology. 71, 12, p. 1791-1793 3 p.

Research output: Article

3 Citations (Scopus)

Baseline level of functional C1-inhibitor correlates with disease severity scores in hereditary angioedema

Kelemen, Z., Moldovan, D., Mihály, E., Visy, B., Széplaki, G., Csuka, D., Füst, G., Farkas, H. & Varga, L., márc. 1 2010, In : Clinical Immunology. 134, 3, p. 354-358 5 p.

Research output: Article

33 Citations (Scopus)

Both positive and negative selection pressures contribute to the polymorphism pattern of the duplicated human CYP21A2 gene

Szabó, J. A., Szilágyi, Á., Doleschall, Z., Patócs, A., Farkas, H., Prohászka, Z., Rácz, K., Füst, G. & Doleschall, M., nov. 29 2013, In : PloS one. 8, 11, e81977.

Research output: Article

8 Citations (Scopus)
36 Citations (Scopus)

C1-inhibitor autoantibodies in SLE

Mészáros, T., Füst, G., Farkas, H., Jakab, L., Temesszentandrási, G., Nagy, G., Kiss, E., Gergely, P., Zeher, M., Griger, Z., Czirják, L., Hóbor, R., Haris, A., Polner, K. & Varga, L., ápr. 2010, In : Lupus. 19, 5, p. 634-638 5 p.

Research output: Article

31 Citations (Scopus)

Canadian 2003 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema

Bowen, T., Cicardi, M., Farkas, H., Bork, K., Kreuz, W., Zingale, L., Varga, L., Martinez-Saguer, I., Aygören-Pürsün, E., Binkley, K., Zuraw, B., Davis, A., Hebert, J., Ritchie, B., Burnham, J., Castaldo, A., Menendez, A., Nagy, I., Harmat, G., Bucher, C. & 18 others, Lacuesta, G., Issekutz, A., Warrington, R., Yang, W., Dean, J., Kanani, A., Stark, D., McCusker, C., Wagner, E., Rivard, G. E., Leith, E., Tsai, E., MacSween, M., Lyanga, J., Serushago, B., Leznoff, A., Waserman, S. & De Serres, J., szept. 1 2004, In : Journal of Allergy and Clinical Immunology. 114, 3, p. 629-637 9 p.

Research output: Article

181 Citations (Scopus)

Changes of coagulation parameters during erythema marginatum in patients with hereditary angioedema

Kőhalmi, K. V., Mező, B., Veszeli, N., Benedek, S., Fehér, A., Holdonner, Á., Jesenak, M., Varga, L. & Farkas, H., ápr. 2020, In : International Immunopharmacology. 81, 106293.

Research output: Article

Open Access
1 Citation (Scopus)

Classification, diagnosis, and approach to treatment for angioedema: Consensus report from the Hereditary Angioedema International Working Group

Cicardi, M., Aberer, W., Banerji, A., Bas, M., Bernstein, J. A., Bork, K., Caballero, T., Farkas, H., Grumach, A., Kaplan, A. P., Riedl, M. A., Triggiani, M., Zanichelli, A. & Zuraw, B., jan. 1 2014, In : Allergy: European Journal of Allergy and Clinical Immunology. 69, 5, p. 602-616 15 p.

Research output: Article

340 Citations (Scopus)

Cleaved kininogen as a biomarker for bradykinin release in hereditary angioedema

Hofman, Z. L. M., de Maat, S., van Doorn, C., Sebastian, S. A. E., Pasterkamp, G., Maas, C., Hofman, Z. L. M., Hack, C. E., Suffritti, C., Zanichelli, A., Cicardi, M., Veszeli, N., Csuka, D., Farkas, H., Renné, T. & Renné, T., dec. 1 2017, In : Journal of Allergy and Clinical Immunology. 140, 6, p. 1700-1703.e8

Research output: Article

17 Citations (Scopus)

Coincidence of hereditary angioedema (HAE) with Crohn's disease

Farkas, H., Gyeney, L., Nemesánszky, E., Káldi, G., Kukán, F., Masszi, I., Soós, J., Bély, M., Farkas, E., Füst, G. & Varga, L., jan. 1 1999, In : Immunological Investigations. 28, 1, p. 43-53 11 p.

Research output: Article

18 Citations (Scopus)

Common genetic variants of the human steroid 21-hydroxylase gene (CYP21A2) are related to differences in circulating hormone levels

Doleschall, M., Szabó, J. A., Pázmándi, J., Szilágyi, Á., Koncz, K., Farkas, H., Tóth, M., Igaz, P., Gláz, E., Prohászka, Z., Korbonits, M., Rácz, K., Füst, G. & Patócs, A., szept. 2014, In : PloS one. 9, 9, e107244.

Research output: Article

7 Citations (Scopus)

Complete kinetic follow-up of symptoms and complement parameters during a hereditary angioedema attack

Veszeli, N., Kőhalmi, K. V., Kajdácsi, E., Gulyás, D., Temesszentandrási, G., Cervenak, L., Farkas, H. & Varga, L., febr. 1 2018, In : Allergy: European Journal of Allergy and Clinical Immunology. 73, 2, p. 516-520 5 p.

Research output: Article

4 Citations (Scopus)
23 Citations (Scopus)

Depressed activation of the lectin pathway of complement in hereditary angioedema

Varga, L., Széplaki, G., Laki, J., Kocsis, A., Kristóf, K., Gál, P., Bajtay, Z., Wieslander, J., Daha, M. R., Garred, P., Madsen, H. O., Füst, G. & Farkas, H., júl. 1 2008, In : Clinical and Experimental Immunology. 153, 1, p. 68-74 7 p.

Research output: Article

12 Citations (Scopus)
3 Citations (Scopus)

Diagnostyka wrodzonego obrzȩku naczynioruchowego

Koőhalmi, K. V., Cervenák, L. & Farkas, H., dec. 1 2018, In : Alergia Astma Immunologia. 23, 4, p. 168-174 7 p.

Research output: Article

Disease expression in women with hereditary angioedema

Bouillet, L., Longhurst, H., Boccon-Gibod, I., Bork, K., Bucher, C., Bygum, A., Caballero, T., Drouet, C., Farkas, H., Massot, C., Nielsen, E. W., Ponard, D. & Cicardi, M., nov. 2008, In : American journal of obstetrics and gynecology. 199, 5, p. 484.e1-484.e4

Research output: Article

94 Citations (Scopus)
24 Citations (Scopus)

Endothelial cell function in patients with hereditary angioedema: Elevated soluble E-selectin level during inter-attack periods

Czícz, J., Schaffer, G., Csuka, D., Walentin, S., Kunde, J., Prohászka, Z., Farkas, H. & Cervenak, L., febr. 1 2012, In : Journal of Clinical Immunology. 32, 1, p. 61-69 9 p.

Research output: Article

15 Citations (Scopus)
56 Citations (Scopus)

Erythema marginatum as an early symptom of hereditary angioedema: Case report of 2 newborns

Martinez-Saguer, I. & Farkas, H., febr. 2016, In : Pediatrics. 137, 2, e20152411.

Research output: Article

15 Citations (Scopus)

Estrogen-independent hereditary angioedema with normal C1 inhibitor function in a 10-year-old boy

Bergmann, M. M., Caubet, J. C., Defendi, F., Farkas, H., Drouet, C. & Eigenmann, P. A., júl. 2013, In : Annals of Allergy, Asthma and Immunology. 111, 1, p. 67-69 3 p.

Research output: Article

2 Citations (Scopus)

Evaluation of the efficacy and safety of home treatment with the recombinant human C1-inhibitor in hereditary angioedema resulting from C1-inhibitor deficiency

Andrási, N., Veszeli, N., Holdonner, Á., Temesszentandrási, G., Kőhalmi, K. V., Varga, L. & Farkas, H., márc. 2020, In : International Immunopharmacology. 80, 106216.

Research output: Article

Open Access

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema

Speletas, M., Szilágyi, Csuka, D., Koutsostathis, N., Psarros, F., Moldovan, D., Magerl, M., Kompoti, M., Varga, L., Maurer, M., Farkas, H. & Germenis, A. E., dec. 1 2015, In : Allergy: European Journal of Allergy and Clinical Immunology. 70, 12, p. 1661-1664 4 p.

Research output: Article

19 Citations (Scopus)

First report of icatibant treatment in a pregnant patient with hereditary angioedema

Farkas, H., Kőhalmi, K. V., Veszeli, N., Tóth, F. & Varga, L., aug. 1 2016, In : Journal of Obstetrics and Gynaecology Research. 42, 8, p. 1026-1028 3 p.

Research output: Article

9 Citations (Scopus)

Flow-mediated vasodilation assay indicates no endothelial dysfunction in hereditary angioedema patients with C1-inhibitor deficiency

Nebenführer, Z., Szabó, E., Kajdácsi, E., Kőhalmi, K. V., Karádi, I., Zsáry, A., Farkas, H. & Cervenák, L., jan. 1 2019, In : Annals of Allergy, Asthma and Immunology. 122, 1, p. 86-92 7 p.

Research output: Article

2 Citations (Scopus)
12 Citations (Scopus)

Functional C1-Inhibitor diagnostics in hereditary angioedema: Assay evaluation and recommendations

Wagenaar-Bos, I. G. A., Drouet, C., Aygören-Pursun, E., Bork, K., Bucher, C., Bygum, A., Farkas, H., Fust, G., Gregorek, H., Hack, C. E., Hickey, A., Joller-Jemelka, H. I., Kapusta, M., Kreuz, W., Longhurst, H., Lopez-Trascasa, M., Madalinski, K., Naskalski, J., Nieuwenhuys, E., Ponard, D. & 7 others, Truedsson, L., Varga, L., Nielsen, E. W., Wagner, E., Zingale, L., Cicardi, M. & van Ham, S. M., szept. 30 2008, In : Journal of Immunological Methods. 338, 1-2, p. 14-20 7 p.

Research output: Article

55 Citations (Scopus)

Gastrointestinal manifestations of hereditary angioedema

Farkas, H., Gyeney, L., Nemesanszky, E., Kaldi, G., Fust, G. & Varga, L., dec. 1 1997, In : European Journal of Internal Medicine. 8, 3, p. 183-187 5 p.

Research output: Article

3 Citations (Scopus)