An evaluation of tests used for the diagnosis and monitoring of C1 inhibitor deficiency: normal serum C4 does not exclude hereditary angio‐oedema - Tarzi, M. D.; Hickey, A.; Förster, T.; Mohammadi, M.; Longhurst, H. J. (Clinical and experimental immunology, 2007)
Keywords: Adult; Aged; Analytical, structural and metabolic biochemistry; Angioedema - diagnosis; Angioedema - genetics; Angioedema - immunology; angio‐oedema; Biological and medical sciences; Biomarkers - blood; C1 inhibitor deficiency; Child; Complement C1 Inhibitor Protein - analysis; Complement C1 Inhibitor Protein - genetics; Complement C1 Inhibitor Protein - immunology; Complement C4 - analysis; False Negative Reactions; Female; Fundamental and applied biological sciences. Psychology; HAE; Humans; Male; Molecular biophysics; Mutation; Reference Values; Sensitivity and Specificity; Translational Studies; Allergy; Immunopathology; Skin disease; Complement C1; Deficiency; Use; Cl inhibitor deficiency; Biochemistry; Biophysics; Hereditary; HAE; angio-oedema; Angioneurotic edema; Surveillance; Serum; Inhibitor; Diagnosis; Molecular biology