日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Autoantibodies Against Factor B and Factor H Without Pathogenic Effects in a Patient with Immune Complex-Mediated Membranoproliferative Glomerulonephritis

免疫复合物介导的膜增生性肾小球肾炎患者体内存在针对因子B和因子H的自身抗体,但无致病作用

Matola, Alexandra T; Csuka, Dorottya; Szilágyi, Ágnes; Rudnicki, Michael; Prohászka, Zoltán; Józsi, Mihály; Uzonyi, Barbara

A Breast Cancer Candidate Locus at 6q Narrowed to 6q15-q21

6q 上的乳腺癌候选基因位点范围缩小至 6q15-q21

Csuka, Dorottya; Freysteinsdottir, Edda S; Johannesdottir, Gudrun; Agnarsson, Bjarni A; Johannsson, Oskar Th; Barkardottir, Rosa B; Arason, Adalgeir

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

应用基于干血斑的蛋白质组学和基因检测方法诊断遗传性血管性水肿

Iuraşcu, Marius-Ionuţ; Balla, Zsuzsanna; Pereira, Catarina; Andrási, Noémi; Varga, Lilian; Csuka, Dorottya; Szilágyi, Ágnes; Tripolszki, Kornelia; Khan, Suliman; Susnea, Iuliana; Bauer, Peter; Cozma, Claudia; Farkas, Henriette

Pregnancy in Complement-Mediated Thrombotic Microangiopathy: Maternal and Neonatal Outcomes

补体介导的血栓性微血管病妊娠:母婴结局

Haninger-Vacariu, Natalja; Gleiss, Andreas; Gaggl, Martina; Aigner, Christof; Kain, Renate; Prohászka, Zoltán; Szilágyi, Ágnes; Csuka, Dorottya; Böhmig, Georg A; Sunder-Plassmann, Raute; Sunder-Plassmann, Gere; Schmidt, Alice

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

一例既往健康幼儿的溶血性尿毒综合征病例报告及文献综述:采用补体抑制疗法成功治疗COVID-19合并溶血性尿毒综合征的病例

Matošević, Matija; Kos, Ivanka; Davidović, Maša; Ban, Maja; Matković, Hana; Jakopčić, Ivan; Vuković Brinar, Ivana; Szilágyi, Ágnes; Csuka, Dorottya; Sinkovits, György; Prohászka, Zoltán; Vrljičak, Kristina; Lamot, Lovro

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

MCPggaac 单倍型与肾移植受者新发血栓性微血管病导致的移植肾存活率低相关。

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

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

血管性血友病因子-ADAMTS13轴、补体激活与COVID-19严重程度和死亡率之间的关联

Sinkovits, György; Réti, Marienn; Müller, Veronika; Iványi, Zsolt; Gál, János; Gopcsa, László; Reményi, Péter; Szathmáry, Beáta; Lakatos, Botond; Szlávik, János; Bobek, Ilona; Prohászka, Zita Z; Förhécz, Zsolt; Mező, Blanka; Csuka, Dorottya; Hurler, Lisa; Kajdácsi, Erika; Cervenak, László; Kiszel, Petra; Masszi, Tamás; Vályi-Nagy, István; Prohászka, Zoltán

The international WAO/EAACI guideline for the management of hereditary angioedema - The 2021 revision and update

WAO/EAACI国际遗传性血管性水肿管理指南——2021年修订版

Maurer, Marcus; Magerl, Markus; Betschel, Stephen; Aberer, Werner; Ansotegui, Ignacio J; Aygören-Pürsün, Emel; Banerji, Aleena; Bara, Noémi-Anna; Boccon-Gibod, Isabelle; Bork, Konrad; Bouillet, Laurence; Boysen, Henrik Balle; Brodszki, Nicholas; Busse, Paula J; Bygum, Anette; Caballero, Teresa; Cancian, Mauro; Castaldo, Anthony J; Cohn, Danny M; Csuka, Dorottya; Farkas, Henriette; Gompels, Mark; Gower, Richard; Grumach, Anete S; Guidos-Fogelbach, Guillermo; Hide, Michihiro; Kang, Hye-Ryun; Kaplan, Allen P; Katelaris, Constance H; Kiani-Alikhan, Sorena; Lei, Wei-Te; Lockey, Richard F; Longhurst, Hilary; Lumry, William; MacGinnitie, Andrew; Malbran, Alejandro; Martinez Saguer, Inmaculada; Matta Campos, Juan José; Nast, Alexander; Nguyen, Dinh; Nieto-Martinez, Sandra A; Pawankar, Ruby; Peter, Jonathan; Porebski, Grzegorz; Prior, Nieves; Reshef, Avner; Riedl, Marc; Ritchie, Bruce; Sheikh, Farrukh Rafique; Smith, William B; Spaeth, Peter J; Stobiecki, Marcin; Toubi, Elias; Varga, Lilian Agnes; Weller, Karsten; Zanichelli, Andrea; Zhi, Yuxiang; Zuraw, Bruce; Craig, Timothy

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

诊断患有遗传性C1抑制剂缺乏症的儿科患者——来自匈牙利血管性水肿参考和卓越中心的经验

Andrási, Noémi; Balla, Zsuzsanna; Visy, Beáta; Szilágyi, Ágnes; Csuka, Dorottya; Varga, Lilian; Farkas, Henriette

Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE)

寻找C1抑制剂缺乏引起的遗传性血管性水肿(C1-INH-HAE)的遗传生物标志物

Parsopoulou, Faidra; Loules, Gedeon; Zamanakou, Maria; Csuka, Dorottya; Szilagyi, Agnes; Kompoti, Maria; Porebski, Grzegorz; Psarros, Fotis; Magerl, Markus; Valerieva, Anna; Staevska, Maria; Obtulowicz, Krystyna; Maurer, Marcus; Speletas, Matthaios; Farkas, Henriette; Germenis, Anastasios E