Sfoglia per Autore
Haemostasis contact system and fibrinolysis in hereditary angioedema (C1-inhibitor deficiency)
1988 M. Cugno, L. C. Bergamaschini, L. D. Uziel, M. Cicardi, A. Agostoni, A. F. Jie, C. Kluft
Fibrinolytic response in normal subjects to venous occlusion and DDAVP infusion
1989 M. Cugno, L.D. Uziel, I. Fabrizi, B. Bottasso, F. Maggiolini, A. Agostoni
The systemic capillary leak syndrome : appearance of interleukin-2-receptor-positivecells during attacks
1990 M. Cicardi, M. Gardinali, G. Bisiani, A. Rosti, P. Allavena, A. Agostoni
Plasma levels of C1- inhibitor complexes and cleaved C1- inhibitor in patients with hereditary angioneurotic edema
1990 M. Cugno, J. Nuijens, E. Hack, A. Eerenberg, D. Frangi, A. Agostoni, M. Cicardi
Physiopathology and management of coagulation during long-term extracorporeal respiratory assistance
1990 L. D. Uziel, M. Cugno, I. Fabrizi, A. Pesenti, L. Gattinoni, A. Agostoni
Nonsensemutations affect C1 inhibitor messenger RNA levels in patients with type Ihereditary angioneurotic edema
1991 D. Frangi, M. Cicardi, A. Sica, F. Colotta, A. Agostoni, A.E. Davis
Plasma levels of tissue-type plasminogen activator and von Willebrand factor in patients with Raynaud's phenomenon
1991 B. Marasini, M. Cugno, A. Agostoni
Long-term treatment of hereditary angioedema with attenuated androgens : a survey of a 13-year experience
1991 M. Cicardi, L. C. Bergamaschini, M. Cugno, E. Hack, G. Agostoni, A. Agostoni
Leucotriene B4 and peptido-leucotriene levels during radiographic contrast media infusion
1992 M. Gardinali, C. Pozzato, L. Conciato, M. di Bello, A. Calcagno, C. Uslenghi, A. Agostoni
Hereditary and acquired C1-inhibitor deficiency : biological and clinical characteristics in 235 patients
1992 A. Agostoni, M. Cicardi
L-arginine therapy in Raynaud's phenomenon?
1992 A. Agostoni, B. Marasini, M. L. Biondi, C. Bassani, A. Cazzaniga, B. Bottasso, M. Cugno
Complement deficiency and antibodyprofile in survivors of meningococcal meningitis due to common serogroups in Italy
1992 R. D'Amelio, A. Agostoni, R. Biselli, M. Brai, G. Caruso, M. Cicardi, A. Corvetta, L. Fontana, G. Misiano, R. Perricone
Replacement therapy in hereditary and acquired angioedema
1992 A. Agostoni, M. Cicardi
Complement activation and polymorphonuclear neutrophil leukocyte elastase in sepsis. Correlation with severity of disease
1992 M. Gardinali, P. Padalino, S. Vesconi, A. Calcagno, S. Ciappellano, L. Conciato, O. Chiara, A. Agostoni, A. Nespoli
Tissue-type plasminogen activator and von Willebrand factor plasma levels as markers of endothelial involvement in patients with Raynaud's phenomenon
1992 B. Marasini, M. Cugno, C. Bassani, M. Stanzani, B. Bottasso, A. Agostoni
DDAVP infusion does not affect plasma levels of endothelin-1 in four normal subjects
1992 B. Marasini, M. Cugno, C. Bassani, I. Fabrizi, B. Bottasso, A. Agostoni
Generation of plasmin during acute attacks of hereditary angioedema
1993 M. Cugno, C. E. Hack, J. P. de Boer, A. J. Eerenberg, A. Agostoni, M. Cicardi
Autoimmune C1 inhibitor deficiency : report of eight patients
1993 M. Cicardi, G. Bisiani, M. Cugno, P. Späth, A. Agostoni
Clinical problems in the C1-inhibitor deficient patient
1993 A. Agostoni, M. Cicardi, M. Cugno, E. Storti
Thrombolytic treatment and complement activation
1994 A. Agostoni, M. Gardinali, D. Frangi, M. Cugno, C. Cafaro, L. Conciato, C. Sponzilli, E. Salmoirago
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