Angioedema Without Wheals: Challenges in Laboratorial Diagnosis

por Grumach, Anete S., Veronez, Camila L., Csuka, Dorottya, Farkas, Henriette
Publicado 2021

163 The Efficacy of Human Plasma-Derived C1-Inhibitor Concentrate Used for Prophylactic Treatment in Patients With Hereditary Angioedema Due to C1-Inhibitor Deficiency

por Csuka, Dorottya, Zotter, Zsuzsanna, Szabó, Erika, Kelemen, Zsuzsanna, Farkas, Henriette
Publicado 2012

458 Differences of Complement Activation Profile between Type I and Type II of Hereditary Angioedema Due to C1-inhibitor Deficiency

por Csuka, Dorottya, Kelemen, Zsuzsanna, Varga, Lilian, Füst, George, Farkas, Henriette
Publicado 2012

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

por Zotter, Zsuzsanna, Veszeli, Nóra, Csuka, Dorottya, Varga, Lilian, Farkas, Henriette
Publicado 2014

Screening for Plasminogen Mutations in Hereditary Angioedema Patients

por Farkas, Henriette, Dóczy, Anna, Szabó, Edina, Varga, Lilian, Csuka, Dorottya
Publicado 2021

The Missing Link: A Case of Severe Adverse Reaction to Histamine in Food and Beverages

por Tamasi, József, Balla, Zsuzsanna, Csuka, Dorottya, Kalabay, László, Farkas, Henriette
Publicado 2022

455 Characterization of the Factors Triggering an Edematous Attack in Hereditary Angioedema

por Zotter, Zsuzsanna, Csuka, Dorottya, Szabó, Erika, Fust, George, Varga, Lilian, Farkas, Henriette
Publicado 2012

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

por Farkas, Henriette, Veszeli, Nora, Szabo, Erika, Csuka, Dorottya, Zotter, Zsuzsanna, Varga, Lilian
Publicado 2015

A case report of a child with sepsis induced multiorgan failure and massive complement consumption treated with a short course of Eculizumab: A case of crosstalk between coagulatio...

por Galic, Slobodan, Csuka, Dorottya, Prohászka, Zoltán, Turudic, Daniel, Dzepina, Petra, Milosevic, Danko
Publicado 2019

Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema

por Szabó, Edina, Csuka, Dorottya, Andrási, Noémi, Varga, Lilian, Farkas, Henriette, Szilágyi, Ágnes
Publicado 2022

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

por Andrási, Noémi, Balla, Zsuzsanna, Visy, Beáta, Szilágyi, Ágnes, Csuka, Dorottya, Varga, Lilian, Farkas, Henriette
Publicado 2022

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

por Zotter, Zsuzsanna, Nagy, Zsolt, Patócs, Attila, Csuka, Dorottya, Veszeli, Nóra, Kőhalmi, Kinga Viktória, Farkas, Henriette
Publicado 2017

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

por Barkai, László József, Sipter, Emese, Csuka, Dorottya, Prohászka, Zoltán, Pilely, Katrine, Garred, Peter, Hosszúfalusi, Nóra
Publicado 2019

86 The Efficacy and Safety of Human Plasma-derived C1-Inhibitor Concentrate Administered for the Treatment of Attacks in Pediatric Patients with Hereditary Angioedema Due to C1-Inh...

por Farkas, Henriette, Csuka, Dorottya, Zotter, Zsuzsanna, Szabó, Erika, Kelemen, Zsuzsanna, Varga, Lilian, Fejes, János, Harmat, George
Publicado 2012

Comprehensive study into the activation of the plasma enzyme systems during attacks of hereditary angioedema due to C1-inhibitor deficiency

por Csuka, Dorottya, Veszeli, Nóra, Imreh, Éva, Zotter, Zsuzsanna, Skopál, Judit, Prohászka, Zoltán, Varga, Lilian, Farkas, Henriette
Publicado 2015

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

por Veszeli, Nóra, Csuka, Dorottya, Zotter, Zsuzsanna, Imreh, Éva, Józsi, Mihály, Benedek, Szabolcs, Varga, Lilian, Farkas, Henriette
Publicado 2015

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

por Cserhalmi, Marcell, Uzonyi, Barbara, Merle, Nicolas S., Csuka, Dorottya, Meusburger, Edgar, Lhotta, Karl, Prohászka, Zoltán, Józsi, Mihály
Publicado 2017

MCPggaac haplotype is associated with poor graft survival in kidney transplant recipients with de novo thrombotic microangiopathy

por Petr, Vojtech, Csuka, Dorottya, Hruba, Petra, Szilágyi, Ágnes, Kollar, Marek, Slavcev, Antonij, Prohászka, Zoltán, Viklicky, Ondrej
Publicado 2022

Atypical hemolytic uremic syndrome triggered by mRNA vaccination against SARS-CoV-2: Case report

por Rysava, Romana, Peiskerova, Martina, Tesar, Vladimir, Benes, Jan, Kment, Martin, Szilágyi, Ágnes, Csuka, Dorottya, Prohászka, Zoltán
Publicado 2022

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

por Kőhalmi, Kinga Viktória, Veszeli, Nóra, Zotter, Zsuzsanna, Csuka, Dorottya, Benedek, Szabolcs, Imreh, Éva, Varga, Lilian, Farkas, Henriette
Publicado 2016