Editorial: C1 inhibitor deficiency and angioedema by Henriette Farkas, Anastasios E. Germenis, Hilary Longhurst

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Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema by Edina Szabó, Dorottya Csuka, Noémi Andrási, Noémi Andrási, Noémi Andrási, Lilian Varga, Henriette Farkas, Henriette Farkas, Ágnes Szilágyi

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Long term follow-up of complement parameters to improve the management of acquired angioedema due to C1-inhibitor deficiency by Zsofia Polai, Zsuzsanna Balla, Lilian Varga, Szabolcs Benedek, Henriette Farkas

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Screening for Plasminogen Mutations in Hereditary Angioedema Patients by Henriette Farkas, Anna Dóczy, Edina Szabó, Lilian Varga, Dorottya Csuka

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Decreased adhesion to endothelium leads to elevated neutrophil granulocyte count in hereditary angioedema patients by Erika Kajdácsi, Zsuzsanna Balla, Zsófia Pólai, László Cervenak, Henriette Farkas

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Serum fetuin-A, tumor necrosis factor alpha and C-reactive protein concentrations in patients with hereditary angioedema with C1-inhibitor deficiency by Bernadett Márkus, Nóra Veszeli, György Temesszentandrási, Henriette Farkas, László Kalabay

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Laryngeal angioedema caused by a rare disease—A case report by Zsofia Polai, Zsuzsanna Balla, Szabolcs Benedek, Erika Kajdacsi, Henriette Farkas

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Angioedema Without Wheals: Challenges in Laboratorial Diagnosis by Anete S. Grumach, Camila L. Veronez, Camila L. Veronez, Dorottya Csuka, Henriette Farkas

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Patient‐physician interactions in hereditary angioedema—Key learnings from the coronavirus disease 2019 pandemic by Marcus Maurer, Thomas Buttgereit, Markus Magerl, Kathrin Schön, Zsusanna Balla, Henriette Farkas

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National survey on clinical and genetic characteristics of patients with hereditary angioedema in Latvia by Adine Kanepa, Inga Nartisa, Dmitrijs Rots, Linda Gailite, Henriette Farkas, Natalja Kurjane

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A novel pathogenetic factor of laryngeal attack in hereditary angioedema? Involvement of protease activated receptor 1 by Henriette Farkas, Csilla Máj, István Kenessey, Anna Sebestyén, Ildikó Krencz, Judit Pápay, László Cervenak

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C1-inhibitor/C1-inhibitor antibody complexes in acquired angioedema due to C1-inhibitor deficiency by Zsofia Polai, Erika Kajdacsi, Laszlo Cervenak, Zsuzsanna Balla, Szabolcs Benedek, Lilian Varga, Henriette Farkas

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The analysis of the effect of the COVID-19 pandemic on patients with hereditary angioedema type I and type II by Dávid Szilágyi, Hanga Réka Horváth, Noémi Andrási, Miklós Soma Kempler, Zsuzsanna Balla, Henriette Farkas

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Hereditary or acquired? Comprehensive genetic testing assists in stratifying angioedema patients by Marija Rozevska, Adine Kanepa, Signe Purina, Linda Gailite, Inga Nartisa, Henriette Farkas, Dmitrijs Rots, Natalja Kurjane

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Patterns of C1-Inhibitor/Plasma Serine Protease Complexes in Healthy Humans and in Hereditary Angioedema Patients by Erika Kajdácsi, Zsófia Jandrasics, Nóra Veszeli, Veronika Makó, Anna Koncz, Dominik Gulyás, Kinga Viktória Köhalmi, Kinga Viktória Köhalmi, György Temesszentandrási, László Cervenak, Péter Gál, József Dobó, Steven de Maat, Coen Maas, Henriette Farkas, Henriette Farkas, Lilian Varga, Lilian Varga

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The characteristics of upper airway edema in hereditary and acquired angioedema with C1‐inhibitor deficiency by Zsuzsanna Balla, Noémi Andrási, Zsófia Pólai, Beáta Visy, Ibolya Czaller, György Temesszentandrási, Dorottya Csuka, Lilian Varga, Henriette Farkas

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Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency—Experience From the Hungarian Angioedema Center of Reference and Excellence by Noémi Andrási, Noémi Andrási, Noémi Andrási, Zsuzsanna Balla, Zsuzsanna Balla, Beáta Visy, Beáta Visy, Ágnes Szilágyi, Dorottya Csuka, Lilian Varga, Henriette Farkas

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Hypersensitivity reactions amongst Hungarian Patients with Hereditary Angioedema due to C1-Inhibitor Deficiency by Hanga Réka Horváth, MD, Dávid Szilágyi, MD, Noémi Andrási, MD, Zsuzsanna Balla, MD, PhD, Beáta Visy, MD, PhD, Henriette Farkas, MD, PhD, DSc

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Attenuated androgen discontinuation in patients with hereditary angioedema: a commented case series by Marcus Maurer, Markus Magerl, Emel Aygören-Pürsün, Konrad Bork, Henriette Farkas, Hilary Longhurst, Sorena Kiani‑Alikhan, Laurence Bouillet, Isabelle Boccon-Gibod, Mauro Cancian, Andrea Zanichelli, David Launay

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Application of a dried blood spot based proteomic and genetic assay for diagnosing hereditary angioedema by Marius‐Ionuţ Iuraşcu, Zsuzsanna Balla, Catarina Pereira, Noémi Andrási, Lilian Varga, Dorottya Csuka, Ágnes Szilágyi, Kornelia Tripolszki, Suliman Khan, Iuliana Susnea, Peter Bauer, Claudia Cozma, Henriette Farkas

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