Nora Veszeli
Budapest POB 2, Kútvölgyi Str. 4
Budapest, BU 1125, Hungary
Budapest, BU 1125, Hungary
Last Updated: 09/26/2026
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Found 35 publications
FHR-5 Serum Levels and CFHR5 Genetic Variations in Patients With Immune Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy.
Journal: Frontiers in immunology
Published: June 03, 2021
Pathways of Neutrophil Granulocyte Activation in Hereditary Angioedema with C1 Inhibitor Deficiency.
Pathways of Neutrophil Granulocyte Activation in Hereditary Angioedema with C1 Inhibitor Deficiency.
Journal: Clinical reviews in allergy & immunology
Published: January 26, 2021
Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome.
Journal: Frontiers in immunology
Published: December 14, 2020
A Novel Homozygous In-Frame Deletion in Complement Factor 3 Underlies Early-Onset Autosomal Recessive Atypical Hemolytic Uremic Syndrome - Case Report.
Journal: Frontiers in immunology
Published: September 21, 2020
Validation of Early Increase in Complement Activation Marker sC5b-9 as a Predictive Biomarker for the Development of Thrombotic Microangiopathy After Stem Cell Transplantation.
Journal: Frontiers in medicine
Published: June 03, 2020
Patterns of C1-Inhibitor/Plasma Serine Protease Complexes in Healthy Humans and in Hereditary Angioedema Patients.
Journal: Frontiers in immunology
Published: December 18, 2019
Clinical Characteristics and Safety of Plasma-Derived C1-Inhibitor Therapy in Children and Adolescents with Hereditary Angioedema-A Long-Term Survey.
Journal: The journal of allergy and clinical immunology. In practice
Published: September 18, 2019
Hereditary angioedema attack: what happens to vasoactive mediators?
Journal: International immunopharmacology
Published: July 17, 2019
Evaluation of the efficacy and safety of home treatment with the recombinant human C1-inhibitor in hereditary angioedema resulting from C1-inhibitor deficiency.
Journal: International immunopharmacology
Published: July 15, 2019
Changes of coagulation parameters during erythema marginatum in patients with hereditary angioedema.
Changes of coagulation parameters during erythema marginatum in patients with hereditary angioedema.
Journal: International immunopharmacology
Published: July 15, 2019
Analysis of the relationship between vitamin D3 level and disease severity in hereditary angioedema
Journal: Orvosi hetilap
Published: June 18, 2019
Serum fetuin-A, tumor necrosis factor alpha and C-reactive protein concentrations in patients with hereditary angioedema with C1-inhibitor deficiency.
Journal: Orphanet journal of rare diseases
Published: September 25, 2018
Last Updated: 09/26/2026