Sfoglia per Autore
Immunoreactive precipitation of C1 inhibitor protein from plasma of normalsubjects and of patients with hereditary angioedema after isoelectric focusing
1986 L.C. Bergamaschini, C. Valle, M. Franzinelli, M. Cicardi, A. Agostoni
Human inhibitor of the first component of complement, C1 : characterization of cDNA clones and localization of the gene to chromosome 11
1986 A.E. Davis, A.S. Whitehead, R.A. Harrison, A. Dauphinais, G.A. Bruns, M. Cicardi, F.S. Rosen
Molecular basis for thedeficiency of complement 1 inhibitor in type I hereditary angioneurotic edema
1987 M. Cicardi, T. Igarashi, F.S. Rosen, A.E. Davis
Restriction fragment length polymorphism of the C1 inhibitor gene in hereditaryangioneurotic edema
1987 M. Cicardi, T. Igarashi, M.S. Kim, D. Frangi, A. Agostoni, A.E. Davis
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
Type I C1inhibitor deficiency with a small messenger RNA resulting from deletion of one exon
1989 T. Ariga, T. Igarashi, N. Ramesh, R. Parad, M. Cicardi, A.E. Davis
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
Identification of a new P1 residuemutation (444Arg----Ser) in a dysfunctional C1 inhibitor protein contained in atype II hereditary angioedema plasma
1990 K.S. Aulak, M. Cicardi, R.A. Harrison
Type II hereditary angioneurotic edema that may result from a single nucleotide change in the codon for alanine-436 in the C1 inhibitor gene
1990 N.J. Levy, N. Ramesh, M. Cicardi, R.A. Harrison, A.E. Davis
Increased levels of soluble interleukin-2 receptors in serum of patients with lung cancer
1990 P. Marino, M. Cugno, A. Preatoni, P. Cori, A. Rosti, L. Frontini, M. Cicardi
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
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
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
Hereditary and acquired C1-inhibitor deficiency : biological and clinical characteristics in 235 patients
1992 A. Agostoni, M. Cicardi
A dysfunctional C1inhibitor protein with a new reactive center mutation (Arg-444-->Leu)
1992 D. Frangi, K.S. Aulak, M. Cicardi, R.A. Harrison, A.E. Davis
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
A hinge region mutation in C1-inhibitor (Ala436-->Thr) results innonsubstrate-like behavior and in polymerization of the molecule
1993 K.S. Aulak, E. Eldering, C.E. Hack, Y.P. Lubbers, R.A. Harrison, A. Mast, M. Cicardi, A.E. Davis
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
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