12.

How Angioedema Quality of Life Questionnaire Can Help Physicians in Treating C1-Inhibitor Deficiency Patients?

Balla Z, Ignácz B, Varga L, Kőhalmi KV, Farkas H.Clin Rev Allergy Immunol. 2021 Aug;61(1):50-59. doi: 10.1007/s12016-021-08850-9. Epub 2021 Mar 3.PMID: 33660212 Free PMC article.

11.

Pathways of Neutrophil Granulocyte Activation in Hereditary Angioedema with C1 Inhibitor Deficiency.

Kajdácsi E, Veszeli N, Mező B, Jandrasics Z, Kőhalmi KV, Ferrara AL, Cervenak L, Varga L, Farkas H.Clin Rev Allergy Immunol. 2021 Jun;60(3):383-395. doi: 10.1007/s12016-021-08847-4. Epub 2021 Feb 19.PMID: 33606193 Free PMC article.

10.

Recombinant human C1 esterase inhibitor for hereditary angioedema attacks: A European registry.

Valerieva A, Staevska MT, Grivcheva-Panovska V, Jesenak M, Kőhalmi KV, Hrubiskova K, Zanichelli A, Bellizzi L, Relan A, Hakl R, Farkas H.World Allergy Organ J. 2021 Apr 22;14(4):100535. doi: 10.1016/j.waojou.2021.100535. eCollection 2021 Apr.PMID: 33995818 Free PMC article.

9.

A follow-up survey of patients with acquired angioedema due to C1-inhibitor deficiency.

Pólai Z, Balla Z, Andrási N, Kőhalmi KV, Temesszentandrási G, Benedek S, Varga L, Farkas H.J Intern Med. 2021 Apr;289(4):547-558. doi: 10.1111/joim.13182. Epub 2020 Nov 20.PMID: 33215769 Free article.

8.

The Importance of Complement Testing in Acquired Angioedema Related to Angiotensin-Converting Enzyme Inhibitors.

Balla Z, Zsilinszky Z, Pólai Z, Andrási N, Kőhalmi KV, Csuka D, Varga L, Farkas H.J Allergy Clin Immunol Pract. 2021 Feb;9(2):947-955. doi: 10.1016/j.jaip.2020.08.052. Epub 2020 Sep 8.PMID: 32916322 Free article.

7.

Clinical Characteristics and Safety of Plasma-Derived C1-Inhibitor Therapy in Children and Adolescents with Hereditary Angioedema-A Long-Term Survey.

Farkas H, Kőhalmi KV, Visy B, Veszeli N, Varga L.J Allergy Clin Immunol Pract. 2020 Jul-Aug;8(7):2379-2383. doi: 10.1016/j.jaip.2020.02.043. Epub 2020 Mar 17.PMID: 32198128 Free article.

 

6.

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 KV, Temesszentandrási G, Cervenak L, Gál P, Dobó J, de Maat S, Maas C, Farkas H, Varga L.Front Immunol. 2020 May 5;11:794. doi: 10.3389/fimmu.2020.00794. eCollection 2020.PMID: 32431708 Free PMC article.

 

5.

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

Kőhalmi KV, Mező B, Veszeli N, Benedek S, Fehér A, Holdonner Á, Jesenak M, Varga L, Farkas H.Int Immunopharmacol. 2020 Apr;81:106293. doi: 10.1016/j.intimp.2020.106293. Epub 2020 Feb 17.PMID: 32078942 Free article.

 

4. 

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 KV, Varga L, Farkas H.Int Immunopharmacol. 2020 Mar;80:106216. doi: 10.1016/j.intimp.2020.106216. Epub 2020 Jan 24.PMID: 31982824 Free article.

 

3.

International Consensus on the Use of Genetics in the Management of Hereditary Angioedema.

Germenis AE, Margaglione M, Pesquero JB, Farkas H, Cichon S, Csuka D, Lera AL, Rijavec M, Jolles S, Szilagyi A, Trascasa ML, Veronez CL, Drouet C, Zamanakou M; Hereditary Angioedema International Working Group.J Allergy Clin Immunol Pract. 2020 Mar;8(3):901-911. doi: 10.1016/j.jaip.2019.10.004. Epub 2019 Oct 24.PMID: 31669336 Review.

2.

[Analysis of the relationship between vitamin D3 level and disease severity in hereditary angioedema].

Visy B, Szilágyi T, Kőhalmi KV, Veszeli N, Varga L, Imreh É, Farkas H.Orv Hetil. 2019 Jun;160(25):987-993. doi: 10.1556/650.2019.31429.PMID: 31203645 Hungarian.

 

1. 

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

Nebenführer Z, Szabó E, Kajdácsi E, Kőhalmi KV, Karádi I, Zsáry A, Farkas H, Cervenak L.Ann Allergy Asthma Immunol. 2019 Jan;122(1):86-92. doi: 10.1016/j.anai.2018.10.004. Epub 2018 Oct 10.PMID: 30312677