George Fust
Budapest, BU, Hungary
Last Updated: 09/26/2026
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Found 21 publications
Common genetic variants of the human steroid 21-hydroxylase gene (CYP21A2) are related to differences in circulating hormone levels.
Journal: PloS one
Published: April 14, 2014
The influence of trigger factors on hereditary angioedema due to C1-inhibitor deficiency.
Journal: Orphanet journal of rare diseases
Published: December 02, 2013
Association of ficolin-3 with severity and outcome of chronic heart failure.
Journal: PloS one
Published: February 06, 2013
Effective humoral immunity against diphtheria and tetanus in patients with systemic lupus erythematosus or myasthenia gravis.
Journal: Molecular immunology
Published: January 24, 2013
Intraspecific evolution of human RCCX copy number variation traced by haplotypes of the CYP21A2 gene.
Journal: Genome biology and evolution
Published: December 18, 2012
The role of ficolins and MASPs in hereditary angioedema due to C1-inhibitor deficiency.
Journal: Molecular immunology
Published: December 13, 2012
Serum concentration of immunoglobulin G-type antibodies against the whole Epstein-Barr nuclear antigen 1 and its aa35-58 or aa398-404 fragments in the sera of patients with systemic lupus erythematosus and multiple sclerosis.
Journal: Clinical and experimental immunology
Published: October 29, 2012
Elevated C1rC1sC1inh levels independently predict atherosclerotic coronary heart disease.
Journal: Molecular immunology
Published: September 26, 2012
A novel assay to quantitate MASP-2/ficolin-3 complexes in serum.
Journal: Journal of immunological methods
Published: September 05, 2012
OS004. A link between the complement system and angiogenic imbalance inpreeclampsia: ficolin-2 deficiency.
Journal: Pregnancy hypertension
Published: July 01, 2012
Last Updated: 09/26/2026