Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Erika Kajdácsi"'
Autor:
Zsolt Förhécz, Tamás Masszi, István Vályi-Nagy, Ilona Bobek, Blanka Mező, P. Reményi, Erika Kajdácsi, B Szathmáry, M. Reti, Petra Kiszel, L Hurler, Dorottya Csuka, György Sinkovits, Zita Z. Prohászka, János Gál, János Szlávik, László Cervenak, Botond Lakatos, László Gopcsa, Zsolt Iványi, Veronika Müller
Publikováno v:
65th Annual Meeting of the Society of Thrombosis and Haemostasis Research.
Autor:
Erika Kajdácsi, Zsófia Jandrasics, Nóra Veszeli, Veronika Makó, Anna Koncz, Dominik Gulyás, Kinga Viktória Köhalmi, György Temesszentandrási, László Cervenak, Péter Gál, József Dobó, Steven de Maat, Coen Maas, Henriette Farkas, Lilian Varga
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 11 (2020)
Frontiers in Immunology, Vol 11 (2020)
C1-inhibitor (C1-INH) is an important regulator of the complement, coagulation, fibrinolytic and contact systems. The quantity of protease/C1-INH complexes in the blood is proportional to the level of the in vivo activation of these four cascade-like
Autor:
Erika Szabó, László Cervenak, Kinga Viktória Kőhalmi, András Zsáry, Erika Kajdácsi, Henriette Farkas, Zsuzsa Nebenfuhrer, István Karádi
Publikováno v:
Annals of allergy, asthmaimmunology : official publication of the American College of Allergy, Asthma,Immunology. 122(1)
Background Hereditary angioedema with C1 inhibitor deficiency (C1-INH-HAE) is a rare, potentially life-threatening disorder characterized by recurrent edematous attacks. The edema formation is the consequence of interaction of bradykinin and various
Autor:
Dominik Gulyás, Kinga Viktória Kőhalmi, Nóra Veszeli, Lilian Varga, Erika Kajdácsi, György Temesszentandrási, László Cervenak, Henriette Farkas
Publikováno v:
Allergy. 73(2)
We studied the kinetics of C1-inhibitor (C1-INH) and other complement parameters in a self-limited edematous attack (EA) in a patient with hereditary angioedema due to C1-INH deficiency to better understand the pathomechanism of the evolution, course
Autor:
László Cervenak, Erika Kajdácsi, Henriette Farkas, Péter K. Jani, Lilian Varga, Zoltán Prohászka, Dorottya Csuka
Publikováno v:
Journal of Allergy and Clinical Immunology. 133:1686-1691
Background Hereditary angioedema (HAE) caused by C1-inhibitor (C1-INH) deficiency (HAE–C1-INH) is a potentially life-threatening rare disease caused by the decreased activity of C1-INH. Lack of C1-INH leads to overproduction of bradykinin, a potent
Publikováno v:
Clinical immunology (Orlando, Fla.). 165
• ANP level is lower in C1-INH HAE patients than in control subjects, and it remains unchanged during edematous attacks.
Autor:
László Cervenak, Erika Kajdácsi, Dorottya Csuka, Henriette Farkas, Lilian Varga, Péter K. Jani, Zoltán Prohászka
Publikováno v:
Journal of clinical immunology. 36(2)
The elevation of bradykinin (BK) level during attacks of hereditary angioedema due to C1-Inhibitor deficiency (C1-INH-HAE) is well known. We previously demonstrated that endothelin-1 (ET-1) level also increases during C1-INH-HAE attacks. Although BK