-
1
-
-
0034541410
-
Frequent de novo mutations and exon deletions in the C1 inhibitor gene of patients with angioedema
-
Pappalardo E, Cicardi M, Duponchel C, et al. Frequent de novo mutations and exon deletions in the C1 inhibitor gene of patients with angioedema. J Allergy Clin Immunol 106: 1147-1154, 2000.
-
(2000)
J. Allergy Clin. Immunol.
, vol.106
, pp. 1147-1154
-
-
Pappalardo, E.1
Cicardi, M.2
Duponchel, C.3
-
2
-
-
0031664687
-
Pathogenic and clinical aspects of C1 inhibitor deficiency
-
Cicardi M, Bergamaschini L, Cugno M, et al. Pathogenic and clinical aspects of C1 inhibitor deficiency. Immunobiology 199: 366-376, 1998.
-
(1998)
Immunobiology
, vol.199
, pp. 366-376
-
-
Cicardi, M.1
Bergamaschini, L.2
Cugno, M.3
-
3
-
-
0025719573
-
C1 inhibitor deficiency: Molecular and immunologic cases of hereditary and acquired angioedema
-
Oltvai ZN, Wong EC, Atkinson JP, Tung KS. C1 inhibitor deficiency: Molecular and immunologic cases of hereditary and acquired angioedema. Lab Invest 65: 381-388, 1991.
-
(1991)
Lab. Invest.
, vol.65
, pp. 381-388
-
-
Oltvai, Z.N.1
Wong, E.C.2
Atkinson, J.P.3
Tung, K.S.4
-
4
-
-
0033368012
-
Activities of the MBL-associated serine proteases (MASPs) and their regulation by natural inhibitors
-
Wong NK, Kojima M, Dobó J, Ambrus G, Sim RB. Activities of the MBL-associated serine proteases (MASPs) and their regulation by natural inhibitors. Mol Immunol 36: 853-861, 1999.
-
(1999)
Mol. Immunol.
, vol.36
, pp. 853-861
-
-
Wong, N.K.1
Kojima, M.2
Dobó, J.3
Ambrus, G.4
Sim, R.B.5
-
5
-
-
0022776774
-
Immune complex in hereditary angioneurotic edema (HANE)
-
D'Amelio R, Perricone R, De Carolis C, Pontesilli O, Matricardi PM, Fontana L. Immune complex in hereditary angioneurotic edema (HANE). J Allergy Clin Immunol 78: 486-487, 1986.
-
(1986)
J. Allergy Clin. Immunol.
, vol.78
, pp. 486-487
-
-
D'Amelio, R.1
Perricone, R.2
De Carolis, C.3
Pontesilli, O.4
Matricardi, P.M.5
Fontana, L.6
-
6
-
-
0024371447
-
Glomerulonephritis and hereditary angioedema: Report of 2 cases
-
Hory B, Haultier JJ. Glomerulonephritis and hereditary angioedema: report of 2 cases. Clin Nephrol 31: 259-263, 1989.
-
(1989)
Clin. Nephrol.
, vol.31
, pp. 259-263
-
-
Hory, B.1
Haultier, J.J.2
-
7
-
-
0026482225
-
Hereditary angioedema complicated with chronic renal failure: Report of sibling cases
-
Nomura H, Tsugawa Y, Koni I, et al. Hereditary angioedema complicated with chronic renal failure: Report of sibling cases. Intern Med 31: 94-97, 1992.
-
(1992)
Intern. Med.
, vol.31
, pp. 94-97
-
-
Nomura, H.1
Tsugawa, Y.2
Koni, I.3
-
8
-
-
0026647424
-
Long-term follow-up of non-systemic lupus erythematosus glomerulonephritis in patients with hereditary angioedema: Report of four cases
-
Pan CG, Strife CF, Ward MK, Spitzer RE, McAdams AJ. Long-term follow-up of non-systemic lupus erythematosus glomerulonephritis in patients with hereditary angioedema: Report of four cases. Am J Kidney Dis 19: 526-531, 1992.
-
(1992)
Am. J. Kidney Dis.
, vol.19
, pp. 526-531
-
-
Pan, C.G.1
Strife, C.F.2
Ward, M.K.3
Spitzer, R.E.4
McAdams, A.J.5
-
9
-
-
0033408447
-
Local bradykinin generation in hereditary angioedema
-
Nussberger J, Cugno M, Cicardi M, Agostoni A. Local bradykinin generation in hereditary angioedema. J Allergy Clin Immunol 104: 1321-1322, 1999.
-
(1999)
J. Allergy Clin. Immunol.
, vol.104
, pp. 1321-1322
-
-
Nussberger, J.1
Cugno, M.2
Cicardi, M.3
Agostoni, A.4
-
10
-
-
0036122075
-
Increased vascular permeability in C1 inhibitor-deficient mice mediated by the bradykinin type 2 receptor
-
Han ED, MacFarlane RC, Mulligan AN, Scafidi J, Davis AE 3rd. Increased vascular permeability in C1 inhibitor-deficient mice mediated by the bradykinin type 2 receptor. J Clin Invest 109: 1057-1063, 2002.
-
(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 III, A.E.5
-
11
-
-
0014972020
-
The complement system in chronic glomerulonephritis: Three newly associated aberrations
-
Pickering RJ, Michael AF Jr, Herdman RC, Good RA, Gewurz H. The complement system in chronic glomerulonephritis: Three newly associated aberrations. J Pediat 78: 30-43, 1971.
-
(1971)
J. Pediat.
, vol.78
, pp. 30-43
-
-
Pickering, R.J.1
Michael Jr., A.F.2
Herdman, R.C.3
Good, R.A.4
Gewurz, H.5
-
12
-
-
0017670813
-
Hereditary angio-edema with mesangiaocapillary glomerulonephritis
-
Plaza J, Malasit P, Kerr DNS. Hereditary angio-edema with mesangiaocapillary glomerulonephritis. Postgrad Med J 53: 627-630, 1977.
-
(1977)
Postgrad. Med. J.
, vol.53
, pp. 627-630
-
-
Plaza, J.1
Malasit, P.2
Kerr, D.N.S.3
-
13
-
-
0018901252
-
Hereditary angioneurotic edema: Immunochemical 'activity' without clinical expression
-
Spitzer RE, Stitzel AE, Urmson JR. Hereditary angioneurotic edema: Immunochemical 'activity' without clinical expression. Int Arch Allergy Appl Immunol 61: 286-292, 1980.
-
(1980)
Int. Arch. Allergy Appl. Immunol.
, vol.61
, pp. 286-292
-
-
Spitzer, R.E.1
Stitzel, A.E.2
Urmson, J.R.3
-
14
-
-
0027529510
-
IgA nephropathy in hereditary angioedema
-
Srinivasan J, Beck P. IgA nephropathy in hereditary angioedema. Postgrad Med J 69: 95-99, 1993.
-
(1993)
Postgrad. Med. J.
, vol.69
, pp. 95-99
-
-
Srinivasan, J.1
Beck, P.2
-
15
-
-
0032715006
-
Tissue kallikrein and kinins in renal disease
-
Naicker S, Naidoo S, Ramsaroop R, Moodley D, Bhoola K. Tissue kallikrein and kinins in renal disease. Immunopharmacol 44: 183-192, 1999.
-
(1999)
Immunopharmacol.
, vol.44
, pp. 183-192
-
-
Naicker, S.1
Naidoo, S.2
Ramsaroop, R.3
Moodley, D.4
Bhoola, K.5
-
16
-
-
0035109612
-
Role of the light chain of high molecular weight kininogen in adhesion, cell-associated proteolysis and angiogenesis
-
Colman RW. Role of the light chain of high molecular weight kininogen in adhesion, cell-associated proteolysis and angiogenesis. Biol Chem 382: 65-70, 2001.
-
(2001)
Biol. Chem.
, vol.382
, pp. 65-70
-
-
Colman, R.W.1
|