-
1
-
-
0026645882
-
Hereditary and acquired C1-inhibitor deficiency: Biological and clinical characteristics in 235 patients
-
Agostoni A, Cicardi M. Hereditary and acquired C1-inhibitor deficiency: Biological and clinical characteristics in 235 patients. Medicine (Baltimore). 1992;71:206-215
-
(1992)
Medicine (Baltimore
, vol.71
, pp. 206-215
-
-
Agostoni, A.1
Cicardi, M.2
-
2
-
-
0031018108
-
Type I hereditary angio-oedema. Variability of clinical presentation and course within two large kindreds
-
Winnewisser J, Rossi M, Spath P, et al. Type I hereditary angio-oedema. Variability of clinical presentation and course within two large kindreds. J Intern Med. 1997;241:39-46
-
(1997)
J Intern Med
, vol.241
, pp. 39-46
-
-
Winnewisser, J.1
Rossi, M.2
Spath, P.3
-
3
-
-
0017077229
-
Hereditary angioedema: The clinical syndrome and its management
-
Frank MM, Gelfand JA, Atkinson JP. Hereditary angioedema: The clinical syndrome and its management. Ann Intern Med. 1976;84:580-593
-
(1976)
Ann Intern Med
, vol.84
, pp. 580-593
-
-
Frank, M.M.1
Gelfand, J.A.2
Atkinson, J.P.3
-
5
-
-
33644759722
-
Symptoms, course, and complications of abdominal attacks in hereditary angioedema due to C1 inhibitor deficiency
-
Bork K, Staubach P, Eckardt AJ, et al. Symptoms, course, and complications of abdominal attacks in hereditary angioedema due to C1 inhibitor deficiency. Am J Gastroenterol. 2006; 101:619-627
-
(2006)
Am J Gastroenterol
, vol.101
, pp. 619-627
-
-
Bork, K.1
Staubach, P.2
Eckardt, A.J.3
-
6
-
-
0023447401
-
Recurrent abdominal pain as the sole manifestation of hereditary angioedema in multiple family members
-
Weinstock BL, Kothari T, Sharma NR, et al. Recurrent abdominal pain as the sole manifestation of hereditary angioedema in multiple family members. Gastroenterol. 1987;93:1116-1118
-
(1987)
Gastroenterol
, vol.93
, pp. 1116-1118
-
-
Weinstock, B.L.1
Kothari, T.2
Sharma, N.R.3
-
7
-
-
0027502225
-
Angioedema presenting as chronic gastrointestinal symptoms
-
Eck SL, Morse JH, Janssen DA, et al. Angioedema presenting as chronic gastrointestinal symptoms. Am J Gastroenterol. 1993;88:436-439
-
(1993)
Am J Gastroenterol
, vol.88
, pp. 436-439
-
-
Eck, S.L.1
Morse, J.H.2
Janssen, D.A.3
-
9
-
-
0029832181
-
Colorectal intussuception: An unusual gastrointestinal complication of hereditary angioedema
-
Witschi A, Krahenbuhl L, Frei E, et al. Colorectal intussuception: An unusual gastrointestinal complication of hereditary angioedema. Int Arch Allergy Immunol. 1996;111:96-98
-
(1996)
Int Arch Allergy Immunol
, vol.111
, pp. 96-98
-
-
Witschi, A.1
Krahenbuhl, L.2
Frei, E.3
-
11
-
-
0036348089
-
Acute abdominal attack of hereditary angioedema associated with ultrasound abnormalities suggestive of acute hepatitis
-
Farkas H, Harmat G, Fekete B, et al. Acute abdominal attack of hereditary angioedema associated with ultrasound abnormalities suggestive of acute hepatitis. Acta Paediatr. 2002;91:971-974
-
(2002)
Acta Paediatr
, vol.91
, pp. 971-974
-
-
Farkas, H.1
Harmat, G.2
Fekete, B.3
-
13
-
-
0034759901
-
Ultrasonography in the diagnosis and monitoring of ascites in acute abdominal attacks of hereditary angioneurotic oedema
-
Farkas H, Harmat G, Kaposi PN, et al. Ultrasonography in the diagnosis and monitoring of ascites in acute abdominal attacks of hereditary angioneurotic oedema. Eur J Gastroenterol Hepatol. 2001;13:1225-1230
-
(2001)
Eur J Gastroenterol Hepatol
, vol.13
, pp. 1225-1230
-
-
Farkas, H.1
Harmat, G.2
Kaposi, P.N.3
-
14
-
-
0028906695
-
Hereditary angioedema: An infrequent cause of abdominal pain with ascites
-
Talavera A, Larraona JL, Ramos JI, et al. Hereditary angioedema: An infrequent cause of abdominal pain with ascites. Am J Gastroenterol. 1995;90:471-474
-
(1995)
Am J Gastroenterol
, vol.90
, pp. 471-474
-
-
Talavera, A.1
Larraona, J.L.2
Ramos, J.I.3
-
15
-
-
0027534838
-
Hereditary angioneurotic edema with severe hypovolemic shock
-
Cohen N, Sharon A, Golik A, et al. Hereditary angioneurotic edema with severe hypovolemic shock. J Clin Gastroenterol. 1993;16:237-239
-
(1993)
J Clin Gastroenterol
, vol.16
, pp. 237-239
-
-
Cohen, N.1
Sharon, A.2
Golik, A.3
-
16
-
-
0035851273
-
Hereditary angioedema: A broad review for clinicians
-
Nzeako UC, Frigas E, Tremaine WJ. Hereditary angioedema: A broad review for clinicians. Arch Intern Med. 2001;161:2417-2429
-
(2001)
Arch Intern Med
, vol.161
, pp. 2417-2429
-
-
Nzeako, U.C.1
Frigas, E.2
Tremaine, W.J.3
-
18
-
-
84859333563
-
Many faces of angioedema: Focus on the diagnosis and the management of abdominal manifestations of hereditary angioedema
-
Nzeako UC, Longhurst HJ. Many faces of angioedema: Focus on the diagnosis and the management of abdominal manifestations of hereditary angioedema. Eur J Gastroenterol Hepatol. 2012;24:353-361
-
(2012)
Eur J Gastroenterol Hepatol
, vol.24
, pp. 353-361
-
-
Nzeako, U.C.1
Longhurst, H.J.2
-
20
-
-
20344383518
-
Hereditary angioedema involving the colon: Endoscopic appearance and review of GI manifestations
-
Koruth JS, Eckardt AJ, Levey JM. Hereditary angioedema involving the colon: Endoscopic appearance and review of GI manifestations. Gastrointest Endoscopy. 2005;61:907-911
-
(2005)
Gastrointest Endoscopy
, vol.61
, pp. 907-911
-
-
Koruth, J.S.1
Eckardt, A.J.2
Levey, J.M.3
-
21
-
-
84866494516
-
Rude awakening: Acute abdominal pain with spontaneous resolution
-
Baines SN, Baines SS, Anis M, et al. Rude Awakening: Acute Abdominal Pain with Spontaneous Resolution. American Journal of Medicine. 2012;125:971-973
-
(2012)
American Journal of Medicine
, vol.125
, pp. 971-973
-
-
Baines, S.N.1
Baines, S.S.2
Anis, M.3
-
22
-
-
38049005317
-
Hereditary angioedema: A current state-of-the-art review VII: Canadian hungarian 2007 international consensus algorithm for the diagnosis, therapy, and management of hereditary angioedema
-
Bowen T, Cicardi M, Bork K, et al. Hereditary angioedema: A current state-of-the-art review, VII: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema. Ann Allergy Asthma Immunol. 2008;100:S30-S40
-
(2008)
Ann Allergy Asthma Immunol
, vol.100
-
-
Bowen, T.1
Cicardi, M.2
Bork, K.3
-
23
-
-
60949104520
-
C1-inhibitor deficiency and angioedema: Molecular mechanisms and clinical progress
-
Cugno M, Zanichelli A, Foieni F, et al. C1-inhibitor deficiency and angioedema: Molecular mechanisms and clinical progress. Trends Mol Med. 2009;15:69-78
-
(2009)
Trends Mol Med
, vol.15
, pp. 69-78
-
-
Cugno, M.1
Zanichelli, A.2
Foieni, F.3
-
24
-
-
0032940370
-
Hereditary angioedema with gastrointestinal involvement: Endoscopic appearance
-
Hara T, Shiotani A, Matsunaka H, et al. Hereditary angioedema with gastrointestinal involvement: Endoscopic appearance. Endoscopy. 1999;31:322-324
-
(1999)
Endoscopy
, vol.31
, pp. 322-324
-
-
Hara, T.1
Shiotani, A.2
Matsunaka, H.3
-
25
-
-
78049495975
-
Diagnosis and management of angioedema with abdominal involvement: A gastroenterology perspective
-
Nzeako UC. Diagnosis and management of angioedema with abdominal involvement: A gastroenterology perspective. World J Gastroenterol. 2010;16:4913-4921
-
(2010)
World J Gastroenterol
, vol.16
, pp. 4913-4921
-
-
Nzeako, U.C.1
-
26
-
-
71949124734
-
Hereditary angio-oedema in Denmark: A nationwide survey
-
Bygum A. Hereditary angio-oedema in Denmark: A nationwide survey. Br J Dermatol. 2009;161:1153-1158
-
(2009)
Br J Dermatol
, vol.161
, pp. 1153-1158
-
-
Bygum, A.1
-
27
-
-
17444402829
-
Hereditary angiooedema due to C1 inhibitor deficiency: Patient registry and approach to the prevalence in Spain
-
Roche O, Blanch A, Caballero T, et al. Hereditary angiooedema due to C1 inhibitor deficiency: Patient registry and approach to the prevalence in Spain. Ann Allergy Asthma Immunol. 2005;94:498-503
-
(2005)
Ann Allergy Asthma Immunol
, vol.94
, pp. 498-503
-
-
Roche, O.1
Blanch, A.2
Caballero, T.3
-
28
-
-
84856654320
-
Hereditary angio-oedema
-
Longhurst HJ, Cicardi M. Hereditary angio-oedema. Lancet. 2012;379:474-481
-
(2012)
Lancet
, vol.379
, pp. 474-481
-
-
Longhurst, H.J.1
Cicardi, M.2
-
29
-
-
84855779242
-
Evidence-based recommendations for the therapeutic management of angioedema owing to hereditary c1 inhibitor deficiency: Consensus report of an international working group
-
Cicardi M, Bork K, Caballero T, et al. Evidence-based recommendations for the therapeutic management of angioedema owing to hereditary C1 inhibitor deficiency: Consensus report of an International Working Group. Allergy. 2012;67:147-157
-
(2012)
Allergy
, vol.67
, pp. 147-157
-
-
Cicardi, M.1
Bork, K.2
Caballero, T.3
-
30
-
-
32844457999
-
Treatment with C1 inhibitor concentrate in abdominal pain attacks of patients with hereditary angio-oedema
-
Bork K, Meng G, Staubach P, et al. Treatment with C1 inhibitor concentrate in abdominal pain attacks of patients with hereditary angio-oedema. Transfusion. 2005;45:1774-1784
-
(2005)
Transfusion
, vol.45
, pp. 1774-1784
-
-
Bork, K.1
Meng, G.2
Staubach, P.3
-
31
-
-
84886570358
-
-
US Food Drug Administration. October 9 Accessed on August 8 2012
-
US Food and Drug Administration. Summary basis for regulatory action - Cinryze. October 9, 2008.http://www.fda.gov/downloads/BiologicsBloodVaccines/ BloodBloodProducts/ ApprovedProducts/LicensedProductsBLAs/FractionatedPlasma Products/UCM129918.pdf. Accessed on August 8, 2012
-
(2008)
Summary Basis For Regulatory Action - Cinryze
-
-
-
32
-
-
0035848333
-
Treatment of 193 episodes of laryngeal edema with C1 inhibitor concentrate in patient with hereditary angio-oedema
-
Bork K, Barnstedt SE. Treatment of 193 episodes of laryngeal edema with C1 inhibitor concentrate in patient with hereditary angio-oedema. Arch Int Med. 2001;161:714-718
-
(2001)
Arch Int Med
, vol.161
, pp. 714-718
-
-
Bork, K.1
Barnstedt, S.E.2
-
33
-
-
34249801766
-
Treatment of acute edema attacks in hereditary angio-oedema with a bradykinin receptor- 2-antagonist (icatibant
-
Bork K, Frank J, Grundt B, et al. Treatment of acute edema attacks in hereditary angio-oedema with a bradykinin receptor- 2-antagonist (icatibant). J Allergy Clin Immunol. 2007;119: 1497-1503
-
(2007)
J Allergy Clin Immunol
, vol.119
, pp. 1497-1503
-
-
Bork, K.1
Frank, J.2
Grundt, B.3
-
34
-
-
78650897413
-
2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema
-
Bowen T, Cicardi M, Farkas H, et al. 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema. Allergy Asthma Clin Immunol. 2010;6:24
-
(2010)
Allergy Asthma Clin Immunol
, vol.6
, pp. 24
-
-
Bowen, T.1
Cicardi, M.2
Farkas, H.3
-
35
-
-
80054010067
-
Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin part II treatment, follow-up, and special situations
-
Caballero T, Baeza ML, Cabanas R, et al. Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part II. Treatment, follow-up, and special situations. J Investig Allergol Clin Immunol. 2011;21:422-441
-
(2011)
J Investig Allergol Clin Immunol
, vol.21
, pp. 422-441
-
-
Caballero, T.1
Baeza, M.L.2
Cabanas, R.3
-
36
-
-
70449727672
-
Efficacy of human C1 esterase inhibitor concentrate compared with placebo in acute hereditary angioedema attacks
-
Craig TJ, Levy RJ, Wasserman RL, et al. Efficacy of human C1 esterase inhibitor concentrate compared with placebo in acute hereditary angioedema attacks. J Allergy Clin Immunol. 2009;124:823-829
-
(2009)
J Allergy Clin Immunol
, vol.124
, pp. 823-829
-
-
Craig, T.J.1
Levy, R.J.2
Wasserman, R.L.3
-
37
-
-
82955243866
-
C1 esterase inhibitor concentrate in 1085 hereditary angioedema attacks - Final results of the I.M.P.A.C.T.2 study
-
Craig TJ, Bewtra AK, Bahna SL, et al. C1 esterase inhibitor concentrate in 1085 hereditary angioedema attacks - Final results of the I.M.P.A.C.T.2 study. Allergy. 2011;66:1604-1611
-
(2011)
Allergy
, vol.66
, pp. 1604-1611
-
-
Craig, T.J.1
Bewtra, A.K.2
Bahna, S.L.3
-
38
-
-
77955299623
-
Nanofiltered C1 inhibitor concentrate for treatment of hereditary angioedema
-
Zuraw BL, Busse PJ, White M, et al. Nanofiltered C1 inhibitor concentrate for treatment of hereditary angioedema. N Eng J Med. 2010;363:513-522
-
(2010)
N Eng J Med
, vol.363
, pp. 513-522
-
-
Zuraw, B.L.1
Busse, P.J.2
White, M.3
-
39
-
-
84886454094
-
-
CSL Behring GmbH. Berinert (C1 Esterase Inhibitor[Human]) [package Insert] Marburg Germany
-
CSL Behring GmbH. Berinert (C1 Esterase Inhibitor[Human]) [package insert]. Marburg, Germany: CSL Behring GmbH; 2009
-
(2009)
CSL Behring GmbH
-
-
-
40
-
-
78049472226
-
Enzymatic pathways in the pathogenesis of hereditary angioedema: The role of C1 inhibitor therapy
-
Kaplan AP. Enzymatic pathways in the pathogenesis of hereditary angioedema: The role of C1 inhibitor therapy. J Allergy Clin Immunol. 2010;126:918-925
-
(2010)
J Allergy Clin Immunol
, vol.126
, pp. 918-925
-
-
Kaplan, A.P.1
-
41
-
-
79952051526
-
Management of acute attacks of hereditary angioedema: Potential role of icatibant
-
Longhurst HJ. Management of acute attacks of hereditary angioedema: Potential role of icatibant. Vasc Health Risk Manag. 2010;6:795-802
-
(2010)
Vasc Health Risk Manag
, vol.6
, pp. 795-802
-
-
Longhurst, H.J.1
-
42
-
-
73349141707
-
Icatibant
-
Deeks ED. Icatibant. Drugs. 2010;70:73-81
-
(2010)
Drugs
, vol.70
, pp. 73-81
-
-
Deeks, E.D.1
-
43
-
-
77955296289
-
Ecallantide for the treatment of acute attacks in hereditary angioedema
-
Cicardi M, Levy RJ, McNeil DL, et al. Ecallantide for the treatment of acute attacks in hereditary angioedema. N Engl J Med. 2010;363:523-531
-
(2010)
N Engl J Med
, vol.363
, pp. 523-531
-
-
Cicardi, M.1
Levy, R.J.2
McNeil, D.L.3
-
44
-
-
77953172116
-
EDEMA4: A phase 3, double blind study of subcutaneous ecallantide treatment for acute attacks of hereditary angioedema
-
Levy RJ, Lumry WR, McNeil DL, et al. EDEMA4: A phase 3, double blind study of subcutaneous ecallantide treatment for acute attacks of hereditary angioedema. Ann Allergy Asthma Immunol. 2010;104:523-529
-
(2010)
Ann Allergy Asthma Immunol
, vol.104
, pp. 523-529
-
-
Levy, R.J.1
Lumry, W.R.2
McNeil, D.L.3
-
45
-
-
84861223735
-
-
Dyax Corp. Kalbitor (Ecallantide) [package Insert] Cambridge MA
-
Dyax Corp. Kalbitor (Ecallantide) [package insert]. Cambridge, MA: Dyax Corp; 2009
-
(2009)
Dyax Corp
-
-
-
46
-
-
0142223817
-
C1-esterase inhibitor substitution in hereditary angioedema
-
Kreuz W, Fischer D, Martinez-Saguer I, et al. C1-esterase inhibitor substitution in hereditary angioedema. Biomed Prog. 1999;12:1-7
-
(1999)
Biomed Prog
, vol.12
, pp. 1-7
-
-
Kreuz, W.1
Fischer, D.2
Martinez-Saguer, I.3
-
47
-
-
34547595509
-
Effective treatment of hereditary angioedema with fresh frozen plasma in an emergency department
-
Pekdemir M, Ersel M, Aksay E, et al. Effective treatment of hereditary angioedema with fresh frozen plasma in an emergency department. J Emerg Med. 2007;33:137-139
-
(2007)
J Emerg Med
, vol.33
, pp. 137-139
-
-
Pekdemir, M.1
Ersel, M.2
Aksay, E.3
-
48
-
-
0017053432
-
Treatment of hereditary angioedema with danazol: Reversal of clinical and biochemical abnormalities
-
Gelfand JA, Sherins RJ, Alling DW, et al. Treatment of hereditary angioedema with danazol: Reversal of clinical and biochemical abnormalities. N Engl J Med. 1976;295:1444-1448
-
(1976)
N Engl J Med
, vol.295
, pp. 1444-1448
-
-
Gelfand, J.A.1
Sherins, R.J.2
Alling, D.W.3
-
49
-
-
0019406629
-
Clinical and biochemical effects of stanozolol therapy for hereditary angioedema
-
Sheffer AL, Fearon DT, Austen KF. Clinical and biochemical effects of stanozolol therapy for hereditary angioedema. J Allergy Clin Immunol. 1981;68:181-187
-
(1981)
J Allergy Clin Immunol
, vol.68
, pp. 181-187
-
-
Sheffer, A.L.1
Fearon, D.T.2
Austen, K.F.3
|