D. Csuka

Z. Prohászka, J. Sinko, G. Kriván, 2018, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema

Á. Szilágyi, H. Farkas, D. Csuka, 2022, Frontiers in Allergy.

FHR-5 Serum Levels and CFHR5 Genetic Variations in Patients With Immune Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy

M. Rudnicki, A. Tislér, G. Mayer, 2021, Frontiers in Immunology.

CFHR5 Genetic Variations and Serum Levels in Patients with Immune-Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy

M. Rudnicki, A. Tislér, J. Reiterová, 2020 .

Sex Differences in Clinical Presentation and Outcomes among Patients with Complement-Gene-Variant-Mediated Thrombotic Microangiopathy

Z. Prohászka, R. Sunder-Plassmann, R. Kain, 2020, Journal of clinical medicine.

Preemptive plasma therapy prevents atypical hemolytic uremic syndrome relapse in kidney transplant recipients.

Z. Prohászka, R. Sunder-Plassmann, R. Kain, 2019, European journal of internal medicine.

Maternal and Fetal Outcomes of Pregnancies in Women with Atypical Hemolytic Uremic Syndrome.

Á. Szilágyi, Z. Prohászka, R. Sunder-Plassmann, 2018, Journal of the American Society of Nephrology : JASN.

The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase ε.

P. Gipson, Mathieu Lemaire, H. Cheong, 2017, Journal of the American Society of Nephrology : JASN.

Genetic analysis and functional characterization of novel mutations in a series of patients with atypical hemolytic uremic syndrome.

Á. Szilágyi, Z. Prohászka, A. Szabó, 2016, Molecular immunology.

Grb2 associated binder 2 couples B-cell receptor to cell survival.

D. Kövesdi, G. Sármay, G. Koncz, 2009, Cellular signalling.

The natural history of hereditary angioedema and the impact of treatment with human C1-inhibitor concentrate during pregnancy: a long-term survey.

H. Farkas, G. Füst, F. Tóth, 2010, European journal of obstetrics, gynecology, and reproductive biology.

Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency—Experience From the Hungarian Angioedema Center of Reference and Excellence

Á. Szilágyi, H. Farkas, D. Csuka, 2022, Frontiers in Allergy.

Treatment of attacks with plasma-derived C1-inhibitor concentrate in pediatric hereditary angioedema patients.

H. Farkas, G. Füst, D. Csuka, 2013, The Journal of allergy and clinical immunology.

The effect of long-term danazol prophylaxis on liver function in hereditary angioedema—a longitudinal study

H. Farkas, Z. Prohászka, G. Füst, 2010, European Journal of Clinical Pharmacology.

Long‐term efficacy of danazol treatment in hereditary angioedema

H. Farkas, G. Füst, K. Bork, 2011, European journal of clinical investigation.

Home treatment of attacks with conestat alfa in hereditary angioedema due to C1-inhibitor deficiency.

H. Farkas, D. Csuka, Z. Zotter, 2014, Allergy and asthma proceedings.

Hereditary Angioedema Due to C1-Inhibitor Deficiency – From a Genetic Point of View

Á. Szilágyi, H. Farkas, D. Csuka, 2015 .

Frequency of the virilising effects of attenuated androgens reported by women with hereditary angioedema

H. Farkas, D. Csuka, Z. Zotter, 2014, Orphanet Journal of Rare Diseases.

Parameters of the classical complement pathway predict disease severity in hereditary angioedema.

H. Farkas, G. Füst, D. Csuka, 2011, Clinical immunology.

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

H. Farkas, G. Füst, G. Szeplaki, 2010, Clinical immunology.

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

H. Farkas, D. Csuka, É. Imreh, 2016, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

The Expanding Spectrum of Mutations in Hereditary Angioedema.

H. Farkas, K. Bork, B. Zuraw, 2021, The journal of allergy and clinical immunology. In practice.

International consensus on the use of genetics in the management of hereditary angioedema.

S. Cichon, M. Margaglione, Á. Szilágyi, 2020, The journal of allergy and clinical immunology. In practice.

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

M. López-Trascasa, H. Farkas, M. Maurer, 2018, Gene.

Idiopathic Nonhistaminergic Acquired Angioedema Versus Hereditary Angioedema.

H. Farkas, D. Csuka, L. Varga, 2018, The journal of allergy and clinical immunology. In practice.

Successful outcome using C1-inhibitor concentrate in acute pancreatitis caused by hereditary angioedema.

H. Farkas, D. Csuka, L. Varga, 2011, Gastroenterology nursing : the official journal of the Society of Gastroenterology Nurses and Associates.

Successful pregnancy outcome after treatment with C1-inhibitor concentrate in a patient with hereditary angioedema and a history of four miscarriages.

H. Farkas, F. Tóth, L. Kőszegi, 2012, European journal of obstetrics, gynecology, and reproductive biology.

Abstracts from the 10th C1-inhibitor deficiency workshop

William H. Yang, A. Szilágyi, M. Margaglione, 2017, Allergy, Asthma & Clinical Immunology.

The influence of trigger factors on hereditary angioedema due to C1-inhibitor deficiency

H. Farkas, D. Csuka, G. Fust, 2014, Orphanet Journal of Rare Diseases.

The Levels of the Lectin Pathway Serine Protease MASP-1 and Its Complex Formation with C1 Inhibitor Are Linked to the Severity of Hereditary Angioedema

K. Skjødt, H. Farkas, P. Garred, 2015, The Journal of Immunology.

Neutrophil activation during attacks in patients with hereditary angioedema due to C1-inhibitor deficiency

H. Farkas, M. Józsi, D. Csuka, 2015, Orphanet Journal of Rare Diseases.

Novel Vasoregulatory Aspects of Hereditary Angioedema: the Role of Arginine Vasopressin, Adrenomedullin and Endothelin-1

H. Farkas, Z. Prohászka, L. Cervenak, 2016, Journal of Clinical Immunology.

Endothelial Cell Function in Patients with Hereditary Angioedema: Elevated Soluble E-selectin Level During Inter-attack Periods

H. Farkas, Z. Prohászka, L. Cervenak, 2012, Journal of Clinical Immunology.

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

H. Farkas, M. Maurer, M. Magerl, 2020, Allergology international : official journal of the Japanese Society of Allergology.

Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor

H. Farkas, M. Bova, S. D. Del Giacco, 2020, Journal of clinical medicine.

The characteristics of upper airway edema in hereditary and acquired angioedema with C1‐inhibitor deficiency

H. Farkas, D. Csuka, L. Varga, 2021, Clinical and translational allergy.

This information is current as the Severity of Hereditary Angioedema Formation with C 1 Inhibitor Are Linked to Protease MASP-1 and Its Complex The Levels of the Lectin Pathway Serine

K. Skjødt, H. Farkas, P. Garred, 2015 .

Definition, aims, and implementation of GA2LEN/HAEi Angioedema Centers of Reference and Excellence

Todor A Popov, T. Zuberbier, N. Papadopoulos, 2020, Allergy.

Strong correlation of high EBNA-1-IgG levels with edematous attacks involving upper airway mucosa in hereditary angioedema due to C1-inhibitor deficiency.

H. Farkas, G. Füst, D. Csuka, 2012, Molecular immunology.

Home treatment of hereditary angioedema with icatibant administered by health care professionals.

H. Farkas, L. Jakab, D. Csuka, 2012, The Journal of allergy and clinical immunology.

Association of celiac disease and hereditary angioedema due to C1-inhibitor deficiency. Screening patients with hereditary angioedema for celiac disease: is it worth the effort?

H. Farkas, G. Füst, Z. Szabó, 2011, European journal of gastroenterology & hepatology.

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

H. Farkas, Z. Prohászka, P. Garred, 2014, The Journal of allergy and clinical immunology.

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

H. Farkas, Z. Prohászka, P. Garred, 2013 .

An abdominal attack of hereditary angio-oedema

H. Farkas, D. Csuka, 2013, The Lancet.

Deep Intronic SERPING1 Gene Variants: Ending One Odyssey and Starting Another?

H. Farkas, A. Germenis, D. Csuka, 2020, Journal of clinical immunology.

Genetic Determinants of C1 Inhibitor Deficiency Angioedema Age of Onset

H. Farkas, M. Maurer, M. Magerl, 2017, International Archives of Allergy and Immunology.

University of Southern Denmark International Consensus on the Use of Genetics in the Management of Hereditary Angioedema Germenis,

S. Cichon, M. Margaglione, H. Farkas, 2020 .

Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome

P. Sánchez-Corral, Á. Szilágyi, Z. Prohászka, 2021, Frontiers in Immunology.

Complement Overactivation and Consumption Predicts In-Hospital Mortality in SARS-CoV-2 Infection

Z. Prohászka, L. Cervenak, T. Masszi, 2021, Frontiers in Immunology.

Hemizygous nonsense variant in the moesin gene (MSN) leads to a new autoimmune phenotype of Immunodeficiency 50

Z. Prohászka, T. Kalmár, G. Késmárky, 2022, Frontiers in Immunology.

Validation of distinct pathogenic patterns in a cohort of membranoproliferative glomerulonephritis patients by cluster analysis

M. Rudnicki, A. Tislér, G. Mayer, 2019, Clinical kidney journal.

Functional Characterization of the Disease-Associated N-Terminal Complement Factor H Mutation W198R

Z. Prohászka, N. Merle, K. Lhotta, 2017, Front. Immunol..

Alternative complement pathway activation during invasive coronary procedures in acute myocardial infarction and stable angina pectoris.

I. Préda, R. Kiss, Z. Prohászka, 2016, Clinica chimica acta; international journal of clinical chemistry.

Complement lectin pathway activation is associated with COVID-19 disease severity, independent of MBL2 genotype subgroups

P. Lyons, Á. Szilágyi, Z. Prohászka, 2023, Frontiers in Immunology.

Elevated C1rC1sC1inh levels independently predict atherosclerotic coronary heart disease.

I. Préda, R. Kiss, G. Füst, 2013, Molecular immunology.

The Role of Mannose-binding Lectin in Infectious Complications of Pediatric Hemato-Oncologic Diseases.

Á. Szilágyi, Z. Prohászka, G. Kovács, 2020, The Pediatric infectious disease journal.

A novel assay to quantitate MASP-2/ficolin-3 complexes in serum.

G. Füst, P. Garred, M. Skjoedt, 2013, Journal of immunological methods.

Association of Low Ficolin–Lectin Pathway Parameters with Cardiac Syndrome X

I. Préda, Z. Prohászka, P. Garred, 2016, Scandinavian journal of immunology.

Elevated Systemic Pentraxin-3 Is Associated With Complement Consumption in the Acute Phase of Thrombotic Microangiopathies

Z. Prohászka, A. Szabó, M. Réti, 2019, Front. Immunol..

Hemolytic uremic syndrome in the setting of COVID-19 successfully treated with complement inhibition therapy: An instructive case report of a previously healthy toddler and review of literature

Á. Szilágyi, Z. Prohászka, K. Vrljicak, 2023, Frontiers in Pediatrics.

Associations between the von Willebrand Factor—ADAMTS13 Axis, Complement Activation, and COVID-19 Severity and Mortality

Z. Prohászka, L. Cervenak, T. Masszi, 2022, Thrombosis and haemostasis.

Efficacy of Eculizumab in a Patient With Immunoadsorption-Dependent Catastrophic Antiphospholipid Syndrome: A Case Report

G. Mayer, Á. Szilágyi, Z. Prohászka, 2014, Medicine.

Decreased Ficolin-3-mediated Complement Lectin Pathway Activation and Alternative Pathway Amplification During Bacterial Infections in Patients With Type 2 Diabetes Mellitus

Z. Prohászka, L. Barkai, P. Garred, 2019, Front. Immunol..

Novel Vasoregulatory Aspects of Hereditary Angioedema: the Role of Arginine Vasopressin, Adrenomedullin and Endothelin-1

H. Farkas, Z. Prohászka, L. Cervenak, 2016, Journal of Clinical Immunology.

Hemolytic uremic syndrome with Mycoplasma pneumoniae infection and membrane cofactor protein mutation – case report.

Á. Szilágyi, Z. Prohászka, D. Drożdż, 2016, Przeglad lekarski.

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

A. Patócs, H. Farkas, Z. Nagy, 2017, Orphanet Journal of Rare Diseases.

Deep Intronic SERPING1 Gene Variants: Ending One Odyssey and Starting Another?

H. Farkas, A. Germenis, D. Csuka, 2020, Journal of Clinical Immunology.

Associations between serum L-arginine and ficolins in the early phase of acute ischemic stroke - A pilot study.

Z. Illés, P. Garred, G. Pusch, 2020, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Functional analysis of the mannose-binding lectin complement pathway in normal pregnancy and preeclampsia.

Z. Prohászka, G. Füst, D. Csuka, 2010, Journal of reproductive immunology.

Short‐term prophylaxis in hereditary angioedema due to deficiency of the C1‐inhibitor – a long‐term survey

H. Farkas, D. Csuka, I. Karádi, 2012, Allergy.

Complement Activation in the Aqueous Humor of Pseudophakic Bullous Keratopathy Patients

G. Füst, J. Németh, I. Süveges, 2012, Ophthalmic Research.

Application of a dried blood spot based proteomic and genetic assay for diagnosing hereditary angioedema

Iuliana Susnea, D. Csuka, M. Iuraşcu, 2023, Clinical and translational allergy.

Functional characterization of two novel non-synonymous alterations in CD46 and a Q950H change in factor H found in atypical hemolytic uremic syndrome patients.

A. Blom, B. Villoutreix, Á. Szilágyi, 2015, Molecular immunology.

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

Á. Szilágyi, H. Farkas, M. Magerl, 2015, Allergy.

Z. Illés, Á. Szilágyi, F. Hudecz, 2013, Clinical and Experimental Immunology.