-
1
-
-
0024146204
-
C1 inhibitor and hereditary angioneurotic edema
-
Davis A.E. C1 inhibitor and hereditary angioneurotic edema. Annu Rev Immunol 6 (1988) 595-628
-
(1988)
Annu Rev Immunol
, vol.6
, pp. 595-628
-
-
Davis, A.E.1
-
2
-
-
0026741755
-
C1-inhibitors and their genes: an update
-
Donaldson V.H., and Bissler J.J. C1-inhibitors and their genes: an update. J Lab Clin Med 119 (1992) 330-333
-
(1992)
J Lab Clin Med
, vol.119
, pp. 330-333
-
-
Donaldson, V.H.1
Bissler, J.J.2
-
3
-
-
49749209550
-
Hereditary angioneurotic edema, II: deficiency of inhibitor for serum globulin permeability factor and/or plasma kallikrein
-
Landerman N.S., Webster M.E., Becker E.L., and Ratcliffe H.E. Hereditary angioneurotic edema, II: deficiency of inhibitor for serum globulin permeability factor and/or plasma kallikrein. J Allergy 33 (1962) 330-341
-
(1962)
J Allergy
, vol.33
, pp. 330-341
-
-
Landerman, N.S.1
Webster, M.E.2
Becker, E.L.3
Ratcliffe, H.E.4
-
4
-
-
50549190821
-
A biochemical abnormality in hereditary angioneurotic edema: absence of serum inhibitor of C' 1-esterase
-
Donaldson V.H., and Evans R.R. A biochemical abnormality in hereditary angioneurotic edema: absence of serum inhibitor of C' 1-esterase. Am J Med 35 (1963) 37-44
-
(1963)
Am J Med
, vol.35
, pp. 37-44
-
-
Donaldson, V.H.1
Evans, R.R.2
-
5
-
-
0000612630
-
Hereditary angioneurotic edema: two genetic variants
-
Rosen F.S., Pensky J., Donaldson V., and Charache P. Hereditary angioneurotic edema: two genetic variants. Science 148 (1965) 957-958
-
(1965)
Science
, vol.148
, pp. 957-958
-
-
Rosen, F.S.1
Pensky, J.2
Donaldson, V.3
Charache, P.4
-
6
-
-
4444347650
-
Canadian 2003 International Consensus algorithm for the diagnosis, therapy, and management of hereditary angioedema
-
Bowen T., Cicardi M., Farkas H., Bork K., Kreuz W., Zingale L., Varga L., et al. Canadian 2003 International Consensus algorithm for the diagnosis, therapy, and management of hereditary angioedema. J Allergy Clin Immunol 114 (2004) 629-637
-
(2004)
J Allergy Clin Immunol
, vol.114
, pp. 629-637
-
-
Bowen, T.1
Cicardi, M.2
Farkas, H.3
Bork, K.4
Kreuz, W.5
Zingale, L.6
Varga, L.7
-
7
-
-
33750528966
-
Mechanism of angioedema in first complement component inhibitor deficiency
-
Davis A.E. Mechanism of angioedema in first complement component inhibitor deficiency. Immunol Allergy Clin North Am 26 (2006) 633-651
-
(2006)
Immunol Allergy Clin North Am
, vol.26
, pp. 633-651
-
-
Davis, A.E.1
-
8
-
-
0022496720
-
Demonstration of modified inactive first component of complement (C1) inhibitor in the plasmas of C1 inhibitor-deficient patients
-
Zuraw B.L., and Curd J.G. Demonstration of modified inactive first component of complement (C1) inhibitor in the plasmas of C1 inhibitor-deficient patients. J Clin Invest 78 (1986) 567-575
-
(1986)
J Clin Invest
, vol.78
, pp. 567-575
-
-
Zuraw, B.L.1
Curd, J.G.2
-
9
-
-
0020520854
-
Kinin formation in hereditary angioedema plasma: evidence against kinin derivation from C2 and in support of "spontaneous" formation of bradykinin
-
Fields T., Ghebrehiwet B., and Kaplan A.P. Kinin formation in hereditary angioedema plasma: evidence against kinin derivation from C2 and in support of "spontaneous" formation of bradykinin. J Allergy Clin Immunol 72 (1983) 54-60
-
(1983)
J Allergy Clin Immunol
, vol.72
, pp. 54-60
-
-
Fields, T.1
Ghebrehiwet, B.2
Kaplan, A.P.3
-
10
-
-
0020614813
-
Prekallikrein activation and high-molecular-weight kininogen consumption in hereditary angioedema
-
Schapira M., Silver L.D., Scott C.F., Schmaier A.H., Prograis Jr. L.J., Curd J.G., et al. Prekallikrein activation and high-molecular-weight kininogen consumption in hereditary angioedema. N Engl J Med 308 (1983) 1050-1053
-
(1983)
N Engl J Med
, vol.308
, pp. 1050-1053
-
-
Schapira, M.1
Silver, L.D.2
Scott, C.F.3
Schmaier, A.H.4
Prograis Jr., L.J.5
Curd, J.G.6
-
11
-
-
0032490360
-
Plasma bradykinin in angio-edema
-
Nussberger J., Cugno M., Amstutz C., Cicardi M., Pellacani A., and Agostoni A. Plasma bradykinin in angio-edema. Lancet 351 (1998) 1693-1697
-
(1998)
Lancet
, vol.351
, pp. 1693-1697
-
-
Nussberger, J.1
Cugno, M.2
Amstutz, C.3
Cicardi, M.4
Pellacani, A.5
Agostoni, A.6
-
12
-
-
0036122075
-
Increased vascular permeability in C1 inhibitor-deficient mice mediated by the bradykinin type 2 receptor
-
Han E.D., MacFarlane R.C., Mulligan A.N., Scafidi J., and Davis A.E. Increased vascular permeability in C1 inhibitor-deficient mice mediated by the bradykinin type 2 receptor. J Clin Invest 109 (2002) 1057-1063
-
(2002)
J Clin Invest
, vol.109
, pp. 1057-1063
-
-
Han, E.D.1
MacFarlane, R.C.2
Mulligan, A.N.3
Scafidi, J.4
Davis, A.E.5
-
13
-
-
0001103785
-
Methyltestosterone therapy for hereditary episodic edema (hereditary angioneurotic edema)
-
Spaulding W.B. Methyltestosterone therapy for hereditary episodic edema (hereditary angioneurotic edema). Ann Intern Med 53 (1960) 739-745
-
(1960)
Ann Intern Med
, vol.53
, pp. 739-745
-
-
Spaulding, W.B.1
-
14
-
-
0015504576
-
Epsilon aminocaproic acid therapy of hereditary angioneurotic edema: a double-blind study
-
Frank M.M., Sergent J.S., Kane M.A., and Alling D.W. Epsilon aminocaproic acid therapy of hereditary angioneurotic edema: a double-blind study. N Engl J Med 286 (1972) 808-812
-
(1972)
N Engl J Med
, vol.286
, pp. 808-812
-
-
Frank, M.M.1
Sergent, J.S.2
Kane, M.A.3
Alling, D.W.4
-
15
-
-
0015531064
-
Tranexamic acid therapy in hereditary angioneurotic edema
-
Sheffer A.L., Austen K.F., and Rosen F.S. Tranexamic acid therapy in hereditary angioneurotic edema. N Engl J Med 287 (1972) 452-454
-
(1972)
N Engl J Med
, vol.287
, pp. 452-454
-
-
Sheffer, A.L.1
Austen, K.F.2
Rosen, F.S.3
-
16
-
-
0014675828
-
Replacement therapy in hereditary angioedema: successful treatment of two patients with fresh frozen plasma
-
Pickering R.J., Good R.A., Kelly J.R., and Gewurz H. Replacement therapy in hereditary angioedema: successful treatment of two patients with fresh frozen plasma. Lancet 1 (1969) 326-330
-
(1969)
Lancet
, vol.1
, pp. 326-330
-
-
Pickering, R.J.1
Good, R.A.2
Kelly, J.R.3
Gewurz, H.4
-
17
-
-
0018903687
-
Replacement therapy in hereditary angioedema: successful treatment of acute episodes of angioedema with partly purified C1 inhibitor
-
Gadek J.E., Hosea S.W., Gelfand J.A., Santaella M., Wickerhauser M., Triantaphyllopoulos D.C., et al. Replacement therapy in hereditary angioedema: successful treatment of acute episodes of angioedema with partly purified C1 inhibitor. N Engl J Med 301 (1980) 542-546
-
(1980)
N Engl J Med
, vol.301
, pp. 542-546
-
-
Gadek, J.E.1
Hosea, S.W.2
Gelfand, J.A.3
Santaella, M.4
Wickerhauser, M.5
Triantaphyllopoulos, D.C.6
-
18
-
-
0029973831
-
Treatment of hereditary angioedema with a vapor-heated C1 inhibitor concentrate
-
Waytes A.T., Rosen F.S., and Frank M.M. Treatment of hereditary angioedema with a vapor-heated C1 inhibitor concentrate. N Engl J Med 334 (1996) 1630-1634
-
(1996)
N Engl J Med
, vol.334
, pp. 1630-1634
-
-
Waytes, A.T.1
Rosen, F.S.2
Frank, M.M.3
-
19
-
-
34948893477
-
Hereditary angioedema: a decade of human C1-inhibitor concentrate therapy
-
Farkas H., Jakab L., Temesszentandrasi G., Visy B., Harmat G., Füst G., et al. Hereditary angioedema: a decade of human C1-inhibitor concentrate therapy. J Allergy Clin Immunol 120 (2007) 941-947
-
(2007)
J Allergy Clin Immunol
, vol.120
, pp. 941-947
-
-
Farkas, H.1
Jakab, L.2
Temesszentandrasi, G.3
Visy, B.4
Harmat, G.5
Füst, G.6
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