• 4990 Citations
  • 35 h-Index
19972020

Research output per year

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Research Output

2020

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

Biological therapy in hereditary angioedema: transformation of a rare disease

Longhurst, H. & Farkas, H., máj. 3 2020, In : Expert Opinion on Biological Therapy. 20, 5, p. 493-501 9 p.

Research output: Review article

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)

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

Hereditary angioedema attack: what happens to vasoactive mediators?

Ferrara, A. L., Bova, M., Petraroli, A., Veszeli, N., Galdiero, M. R., Braile, M., Marone, G., Cristinziano, L., Marcella, S., Modestino, L., Farkas, H. & Loffredo, S., jan. 2020, In : International Immunopharmacology. 78, 106079.

Research output: Article

Open Access
1 Citation (Scopus)
Open Access

Long-term efficacy and safety of subcutaneous C1-inhibitor in women with hereditary angioedema: Subgroup analysis from an open-label extension of a phase 3 trial

Levy, D. S., Farkas, H., Riedl, M. A., Hsu, F. I., Brooks, J. P., Cicardi, M., Feuersenger, H., Pragst, I. & Reshef, A., febr. 4 2020, In : Allergy, Asthma and Clinical Immunology. 16, 1, 8.

Research output: Article

Open Access

Patterns of C1-Inhibitor/Plasma Serine Protease Complexes in Healthy Humans and in Hereditary Angioedema Patients

Kajdácsi, E., Jandrasics, Z., Veszeli, N., Makó, V., Koncz, A., Gulyás, D., Köhalmi, K. V., Temesszentandrási, G., Cervenak, L., Gál, P., Dobó, J., de Maat, S., Maas, C., Farkas, H. & Varga, L., máj. 5 2020, In : Frontiers in immunology. 11, 794.

Research output: Article

Open Access
2019

Delayed diagnosis of hereditary angioedema with C1-inhibitor deficiency in iranian children and adolescents

Ayazi, M., Fazlollahi, M. R., Mohammadzadeh, I., Fayezi, A., Nabavi, M., Mahdaviani, S. A., Movahedi, M., Heidarzadeh, M., Saghafi, S., Shokouhi Shoormasti, R., Mohammadian, S., Farkas, H. & Pourpak, Z., máj. 2019, In : Pediatric Allergy and Immunology. 30, 3, p. 395-398 4 p.

Research output: Letter

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)
6 Citations (Scopus)

Recombinant human C1 esterase inhibitor treatment for hereditary angioedema attacks in children

Reshef, A., Grivcheva-Panovska, V., Kessel, A., Kivity, S., Klimaszewska-Rembiasz, M., Moldovan, D., Farkas, H., Gutova, V., Fritz, S., Relan, A., Giannetti, B. & Magerl, M., aug. 2019, In : Pediatric Allergy and Immunology. 30, 5, p. 562-568 7 p.

Research output: Article

Open Access
3 Citations (Scopus)
Open Access
2018

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)

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)

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

Health-Related Quality of Life with Subcutaneous C1-Inhibitor for Prevention of Attacks of Hereditary Angioedema

Lumry, W. R., Craig, T., Zuraw, B., Longhurst, H., Baker, J., Li, H. H., Bernstein, J. A., Anderson, J., Riedl, M. A., Manning, M. E., Keith, P. K., Levy, D. S., Caballero, T., Banerji, A., Gower, R. G., Farkas, H., Lawo, J. P., Pragst, I., Machnig, T. & Watson, D. J., szept. 1 2018, In : Journal of Allergy and Clinical Immunology: In Practice. 6, 5, p. 1733-1741.e3

Research output: Article

16 Citations (Scopus)
6 Citations (Scopus)

Idiopathic Nonhistaminergic Acquired Angioedema Versus Hereditary Angioedema

Andrási, N., Veszeli, N., Kőhalmi, K. V., Csuka, D., Temesszentandrási, G., Varga, L. & Farkas, H., júl. 1 2018, In : Journal of Allergy and Clinical Immunology: In Practice. 6, 4, p. 1205-1208 4 p.

Research output: Article

3 Citations (Scopus)

Investigational drugs in phase I and phase II clinical trials for hereditary angioedema

Farkas, H., Debreczeni, M. L. & Kőhalmi, K. V., jan. 2 2018, In : Expert Opinion on Investigational Drugs. 27, 1, p. 87-103 17 p.

Research output: Review article

4 Citations (Scopus)

Lanadelumab for the Prophylactic Treatment of Hereditary Angioedema with C1 Inhibitor Deficiency: A Review of Preclinical and Phase I Studies

Busse, P. J., Farkas, H., Banerji, A., Lumry, W. R., Longhurst, H. J., Sexton, D. J. & Riedl, M. A., jan. 1 2018, (Accepted/In press) In : BioDrugs.

Research output: Article

5 Citations (Scopus)
6 Citations (Scopus)

Secreted phospholipases A2 in hereditary angioedema with C1-inhibitor deficiency

Loffredo, S., Ferrara, A. L., Bova, M., Borriello, F., Suffritti, C., Veszeli, N., Petraroli, A., Galdiero, M. R., Varricchi, G., Granata, F., Zanichelli, A., Farkas, H., Cicardi, M., Lambeau, G. & Marone, G., júl. 23 2018, In : Frontiers in immunology. 9, JUL, 1721.

Research output: Article

8 Citations (Scopus)

Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency

Loules, G., Zamanakou, M., Parsopoulou, F., Vatsiou, S., Psarros, F., Csuka, D., Porebski, G., Obtulowicz, K., Valerieva, A., Staevska, M., López-Lera, A., López-Trascasa, M., Moldovan, D., Magerl, M., Maurer, M., Speletas, M., Farkas, H. & Germenis, A. E., aug. 15 2018, In : Gene. 667, p. 76-82 7 p.

Research output: Article

13 Citations (Scopus)

Wybrane aspekty genotypowania wrodzonego obrzȩku naczynioruchowego w erze NGS: Gen F12

Vatsiou, S., Zamanakou, M., Loules, G., González-Quevedo, T., Porȩbski, G., Juchacz, A., Bova, M., Suffritti, C., Firinu, D., Csuka, D., Manousakis, E., Valerieva, A., Staevska, M., Magerl, M., Farkas, H. & Germenis, A. E., dec. 2018, In : Alergia Astma Immunologia. 23, 4, p. 205-210 6 p.

Research output: Article

2017
4 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)

Genetic determinants of C1 inhibitor deficiency angioedema age of onset

Gianni, P., Loules, G., Zamanakou, M., Kompoti, M., Csuka, D., Psarros, F., Magerl, M., Moldovan, D., Maurer, M., Speletas, M. G., Farkas, H. & Germenis, A. E., jan. 1 2017, In : International archives of allergy and immunology. 174, 3-4, p. 200-204 5 p.

Research output: Article

9 Citations (Scopus)

Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency

Zotter, Z., Nagy, Z., Patócs, A., Csuka, D., Veszeli, N., Kohalmi, K. V. & Farkas, H., jan. 10 2017, In : Orphanet journal of rare diseases. 12, 1, 5.

Research output: Article

2 Citations (Scopus)

Health-related quality of life among children with hereditary angioedema

Engel-Yeger, B., Farkas, H., Kivity, S., Veszeli, N., Kőhalmi, K. V. & Kessel, A., jún. 1 2017, In : Pediatric Allergy and Immunology. 28, 4, p. 370-376 7 p.

Research output: Article

18 Citations (Scopus)
60 Citations (Scopus)

Reply

Joseph, K., Constantino-Silva, R. N., Grumach, A. S., Feldweg, A., Wright, L., Frank, N., Vuzman, D., Sharma, R., Suffritti, C., Cicardi, M., Varga, L., Farkas, H., Bork, K. & Kaplan, A. P., máj. 2017, In : Journal of Allergy and Clinical Immunology. 139, 5, p. 1720-1721 2 p.

Research output: Letter

2 Citations (Scopus)

The relationship between anxiety and quality of life in children with hereditary angioedema

Kessel, A., Farkas, H., Kivity, S., Veszeli, N., Kőhalmi, K. V. & Engel-Yeger, B., nov. 1 2017, In : Pediatric Allergy and Immunology. 28, 7, p. 692-698 7 p.

Research output: Article

10 Citations (Scopus)

The role of the complement system in hereditary angioedema

Csuka, D., Veszeli, N., Varga, L., Prohászka, Z. & Farkas, H., szept. 2017, In : Molecular Immunology. 89, p. 59-68 10 p.

Research output: Review article

19 Citations (Scopus)

Treatment Effect and Safety of Icatibant in Pediatric Patients with Hereditary Angioedema

Farkas, H., Reshef, A., Aberer, W., Caballero, T., McCarthy, L., Hao, J., Nothaft, W., Schranz, J., Bernstein, J. A. & Li, H. H., nov. 2017, In : Journal of Allergy and Clinical Immunology: In Practice. 5, 6, p. 1671-1678.e2

Research output: Article

20 Citations (Scopus)
2016

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)
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)

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

Martinez-Saguer, I. & Farkas, H., febr. 1 2016, In : Pediatrics. 137, 2, e20152411.

Research output: Article

15 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)

Icatibant as acute treatment for hereditary angioedema in adults

Farkas, H., máj. 14 2016, (Accepted/In press) In : Expert Review of Clinical Pharmacology. p. 1-10 10 p.

Research output: Article

7 Citations (Scopus)
10 Citations (Scopus)

Psychometric Field Study of Hereditary Angioedema Quality of Life Questionnaire for Adults: HAE-QoL

Prior, N., Remor, E., Pérez-Fernández, E., Caminoa, M., Gómez-Traseira, C., Gayá, F., Aabom, A., Aberer, W., Betschel, S., Boccon-Gibod, I., Bouillet, L., Bygum, A., Csuka, D., Farkas, H., Gomide, M., Grumach, A., Leibovich, I., Malbran, A., Moldovan, D., Mihaly, E. & 9 others, Obtulowicz, K., Perpén, C., Peveling-Oberhag, A., Porebski, G., Chavannes, C. R., Reshef, A., Staubach, P., Wiednig, M. & Caballero, T., máj. 1 2016, In : Journal of Allergy and Clinical Immunology: In Practice. 4, 3, p. 464-473.e4

Research output: Article

19 Citations (Scopus)

Risk of thromboembolism in patients with hereditary angioedema treated with plasma-derived C1-inhibitor

Farkas, H., Kohalmi, K. V., Veszeli, N., Zotter, Z., Várnai, K. & Varga, L., márc. 1 2016, In : Allergy and Asthma Proceedings. 37, 2, p. 164-170 7 p.

Research output: Article

13 Citations (Scopus)

The effect of long-term danazol treatment on haematological parameters in hereditary angioedema Rare immune deficiencies

Kohalmi, K. V., Veszeli, N., Zotter, Z., Csuka, D., Benedek, S., Imreh, É., Varga, L. & Farkas, H., febr. 25 2016, In : Orphanet journal of rare diseases. 11, 1, 18.

Research output: Article

6 Citations (Scopus)

Thromboembolierisiko bei hereditärem Angioödem unter Therapie mit plasmatischem C1-Esterase-Inhibitor

Farkas, H., Köhalmi, K. V., Veszeli, N., Zotter, Z., Värnai, K. & Varga, L., márc. 1 2016, In : Vasomed. 28, 2, p. 72-73 2 p.

Research output: Article

Thyroid hormones and complement parameters in hereditary angioedema with C1-inhibitor deficiency

Czaller, I., Csuka, D., Zotter, Z., Veszeli, N., Takács, E., Imreh, É., Varga, L. & Farkas, H., aug. 1 2016, In : Annals of Allergy, Asthma and Immunology. 117, 2, p. 175-179 5 p.

Research output: Article

1 Citation (Scopus)