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Molecular Immunology|January 19, 2007
Relationship between copy number of genes (C4A, C4B) encoding the fourth component of complement and the clinical course of hereditary angioedema (HAE)Bernadett Blaskó, Gábor Széplaki, Lilian Varga, et al.Journal of Immunological Methods|November 13, 2012
A novel assay to quantitate MASP-2/ficolin-3 complexes in serumDorottya Csuka, Lea Munthe-Fog, Mikkel-Ole Skjoedt, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|March 14, 2007
Lipid, haemostatic and inflammatory variables in relation to the estrogen receptor alpha (ESR1) PvuII and XbaI gene polymorphismsAttila Molvarec, Bálint Nagy, Margit Kovács, et al.Molecular Immunology|June 6, 2006
C1-inhibitor (C1-INH) autoantibodies in hereditary angioedema. Strong correlation with the severity of disease in C1-INH concentrate naïve patientsLilian Varga, Gábor Széplaki, Beáta Visy, et al.Cytokine|February 14, 2006
Decreased frequency of the TNF2 allele of TNF-alpha -308 promoter polymorphism is associated with lacunar infarctionPéter Harcos, Judit Laki, Petra Kiszel, et al.Journal of Lipid Research|October 7, 2006
Novel anti-cholesterol monoclonal immunoglobulin G antibodies as probes and potential modulators of membrane raft-dependent immune functionsAdrienn Bíró, László Cervenak, Andrea Balogh, et al.The Journal of Allergy and Clinical Immunology|September 1, 2007
Hereditary angioedema: a decade of human C1-inhibitor concentrate therapyHenriette Farkas, László Jakab, György Temesszentandrási, et al.Immunology|January 25, 2007
Studies on the interactions between C-reactive protein and complement proteinsAdrienn Bíró, Zita Rovó, Diana Papp, et al.European Journal of Gastroenterology & Hepatology|April 11, 2002
Human fetuin/alpha2HS-glycoprotein level as a novel indicator of liver cell function and short-term mortality in patients with liver cirrhosis and liver cancerLászló Kalabay, Lajos Jakab, Zoltán Prohászka, et al.European Journal of Gastroenterology & Hepatology|February 10, 2011
Association of celiac disease and hereditary angioedema due to C1-inhibitor deficiency. Screening patients with hereditary angioedema for celiac disease: is it worth the effort?Dorottya Csuka, Zsuzsanna Kelemen, Ibolya Czaller, et al.Pageof 10