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1 . Academic Journal
Application of a dried blood spot based proteomic and genetic assay for diagnosing hereditary angioedema
저자
by
Marius‐Ionuţ Iuraşcu
;
Zsuzsanna Balla
;
Catarina Pereira
;
Noémi Andrási
;
Lilian Varga
, et al.
소스
Clinical and Translational Allergy, Vol 13, Iss 11, Pp n/a-n/a (2023)
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7 . Academic Journal
Pregnancy in Complement-Mediated Thrombotic Microangiopathy: Maternal and Neonatal OutcomesPlain Language Summary
저자
by
Natalja Haninger-Vacariu
;
Andreas Gleiss
;
Martina Gaggl
;
Christof Aigner
;
Renate Kain
, et al.
소스
Kidney Medicine, Vol 5, Iss 7, Pp 100669- (2023)
Full Text (ScienceDirect)
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7 . Academic Journal
Complement lectin pathway activation is associated with COVID-19 disease severity, independent of MBL2 genotype subgroups
저자
by
Lisa Hurler
;
Ágnes Szilágyi
;
Federica Mescia
;
Laura Bergamaschi
;
Blanka Mező
, et al.
소스
Frontiers in Immunology, Vol 14 (2023)
Open Access (DOAJ)
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7 . Academic Journal
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
저자
by
Matija Matošević
;
Ivanka Kos
;
Maša Davidović
;
Maja Ban
;
Hana Matković
, et al.
소스
Frontiers in Pediatrics, Vol 11 (2023)
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7 . Academic Journal
Atypical hemolytic uremic syndrome triggered by mRNA vaccination against SARS-CoV-2: Case report
저자
by
Romana Rysava
;
Martina Peiskerova
;
Vladimir Tesar
;
Jan Benes
;
Martin Kment
, et al.
소스
Frontiers in Immunology, Vol 13 (2022)
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7 . Academic Journal
MCPggaac haplotype is associated with poor graft survival in kidney transplant recipients with de novo thrombotic microangiopathy
저자
by
Vojtech Petr
;
Dorottya Csuka
;
Petra Hruba
;
Ágnes Szilágyi
;
Marek Kollar
, et al.
소스
Frontiers in Immunology, Vol 13 (2022)
Open Access (DOAJ)
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7 . Academic Journal
Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE)
저자
by
Faidra Parsopoulou
;
Gedeon Loules
;
Maria Zamanakou
;
Dorottya Csuka
;
Agnes Szilagyi
, et al.
소스
Frontiers in Allergy, Vol 3 (2022)
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7 . Academic Journal
Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency—Experience From the Hungarian Angioedema Center of Reference and Excellence
저자
by
Noémi Andrási
;
Zsuzsanna Balla
;
Beáta Visy
;
Ágnes Szilágyi
;
Dorottya Csuka
, et al.
소스
Frontiers in Allergy, Vol 3 (2022)
Open Access (DOAJ)
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7 . Academic Journal
Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema
저자
by
Edina Szabó
;
Dorottya Csuka
;
Noémi Andrási
;
Lilian Varga
;
Henriette Farkas
, et al.
소스
Frontiers in Allergy, Vol 3 (2022)
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7 . Academic Journal
FHR-5 Serum Levels and CFHR5 Genetic Variations in Patients With Immune Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy
저자
by
Nóra Garam
;
Marcell Cserhalmi
;
Zoltán Prohászka
;
Ágnes Szilágyi
;
Nóra Veszeli
, et al.
소스
Frontiers in Immunology, Vol 12 (2021)
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