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Medicine|July 1, 1992
Hereditary and acquired C1-inhibitor deficiency: biological and clinical characteristics in 235 patientsA Agostoni, M Cicardi
Drug Safety|August 2, 2001
Drug-induced angioedema without urticariaA Agostoni, M Cicardi
Annali Italiani Di Medicina Interna : Organo Ufficiale Della Societa Italiana Di Medicina Interna|January 1, 1997
Angioedema due to angiotensin-converting enzyme inhibition: an association frequently unrecognizedM Cicardi, L Conciato, A Agostoni
International Journal of Clinical & Laboratory Research|January 1, 1992
Peripheral edema due to increased vascular permeability: a clinical appraisalA Agostoni, M Cicardi, W Porreca
The Journal of Allergy and Clinical Immunology|May 1, 1994
Activation of the contact system and fibrinolysis in autoimmune acquired angioedema: a rationale for prophylactic use of tranexamic acidM Cugno, M Cicardi, A Agostoni
Immunopharmacology|June 1, 1996
Activation of factor XII and cleavage of high molecular weight kininogen during acute attacks in hereditary and acquired C1-inhibitor deficienciesM Cugno, M Cicardi, R Coppola, et al.
Behring Institute Mitteilungen|December 1, 1993
Clinical problems in the C1-inhibitor deficient patientA Agostoni, M Cicardi, M Cugno, et al.
Journal of Clinical Pathology|July 1, 1982
Effect of treatment with 17 alpha-alkylated androgens on C4 conversion products in hereditary angioedema studied by crossed immunoelectrophoresisL Bergamaschini, M Cicardi, A Tucci, et al.
Klinische Wochenschrift|August 15, 1978
Treatment of hereditary angioedemaB Marasini, M Cicardi, G C Martignoni, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|October 1, 1986
Immunoreactive precipitation of C1 inhibitor protein from plasma of normal subjects and of patients with hereditary angioedema after isoelectric focusingL Bergamaschini, C Valle, M Franzinelli, et al.
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