Lilian Varga

University Hospital Bratislava — SK

Medicine · Health Sciences

40h-index6.2kcitations291works0.52yr avg
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Research Topics

Coagulation, Bradykinin, Polyphosphates, and Angioedema(150), Complement system in diseases(50), Autoimmune Bullous Skin Diseases(44), Vitamin K Research Studies(41), Hemophilia Treatment and Research(35)

Publications290 total

Hematology and muscle signature of elite master endurance runner with thalassemia
Science & Sports·2025
How can the monitoring of complement parameters help to treat angioedema due to C1-inhibitor deficiency?
2024· 1 citedOpen Access
Application of a dried blood spot based proteomic and genetic assay for diagnosing hereditary angioedema
Clinical and Translational Allergy·2023· 12 citedOpen Access
171 The dominant form of the C1 inhibitor R444C variant causing type II hereditary angioedema is its covalent adduct with serum albumin explaining elevated levels
Immunobiology·2023
C1-inhibitor/C1-inhibitor antibody complexes in acquired angioedema due to C1-inhibitor deficiency
Orphanet Journal of Rare Diseases·2023· 4 citedOpen Access
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PubMed·2023
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PubMed·2023Open Access
Long term follow-up of complement parameters to improve the management of acquired angioedema due to C1-inhibitor deficiency
Heliyon·2022· 1 citedOpen Access
Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency—Experience From the Hungarian Angioedema Center of Reference and Excellence
Frontiers in Allergy·2022· 12 citedOpen Access
Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema
Frontiers in Allergy·2022· 8 citedOpen Access
The international WAO/EAACI guideline for the management of hereditary angioedema – The 2021 revision and update
World Allergy Organization Journal·2022· 141 citedOpen Access
The international WAO/EAACI guideline for the management of hereditary angioedema—The 2021 revision and update
Allergy·2022· 442 citedOpen Access
The characteristics of upper airway edema in hereditary and acquired angioedema with C1‐inhibitor deficiency
Clinical and Translational Allergy·2021· 12 citedOpen Access
Acquired Angioedema Due to C1 inhibitor Deficiency Caused by Non-Hodgkin Lymphoma in a Patient with Myasthenia Gravis
Revista română de medicină de laborator·2021Open Access
The Global Registry for Hereditary Angioedema due to C1-Inhibitor Deficiency
Clinical Reviews in Allergy & Immunology·2021· 22 citedOpen Access
Screening for Plasminogen Mutations in Hereditary Angioedema Patients
Genes·2021· 6 citedOpen Access
How Angioedema Quality of Life Questionnaire Can Help Physicians in Treating C1-Inhibitor Deficiency Patients?
Clinical Reviews in Allergy & Immunology·2021· 23 citedOpen Access
Pathways of Neutrophil Granulocyte Activation in Hereditary Angioedema with C1 Inhibitor Deficiency
Clinical Reviews in Allergy & Immunology·2021· 8 citedOpen Access
Triggering receptor expressed on myeloid cells 1 and 2 in patients with chronic maxillary sinusitis
Bratislavské lekárske listy/Bratislava medical journal·2021Open Access
A follow‐up survey of patients with acquired angioedema due to C1‐inhibitor deficiency
Journal of Internal Medicine·2020· 20 cited
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Frequent Co-authors

Henriette Farkas(39), George Füst(27), Dorottya Csuka(14), István Karádi(13), Zoltán Prohászka(11), George Harmat(9), Gábor Széplaki(9), Konrad Bork(8), Beáta Visy(7), László Jakab(6), B. Fekete(6), Tom Bowen(5), Hilary Longhurst(5), Emel Aygören‐Pürsün(5), Zsuzsanna Zotter(5), László Cervenak(5), Nóra Veszeli(5), Marco Cicardi(4), Bruce L. Zuraw(4), Timothy Craig(4)