8. Hereditary angioedema

Journal of Allergy and Clinical Immunology

Volumn 121, Issue 2 SUPPL. 2, 2008, Pages

  Frank, Michael M ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

androgens; antifibrinolytics; bradykinin; C1 esterase inhibitor; C1 inhibitor; complement; danazol; Hereditary angioedema

Indexed keywords

ADRENALIN; AMINOCAPROIC ACID; ANDROGEN; ANTIHISTAMINIC AGENT; BRADYKININ; COMPLEMENT COMPONENT C1S INHIBITOR; DANAZOL; ESTROGEN; GLUCOCORTICOID; ICATIBANT; OXANDROLONE;

ABDOMINAL PAIN; ANGIONEUROTIC EDEMA; ANTIGENICITY; ANXIETY; ARTICLE; CREATINE KINASE BLOOD LEVEL; DRUG EFFICACY; EDEMA; GASTROINTESTINAL MUCOSA; GENE MUTATION; HAIR LOSS; HEADACHE; HEMATURIA; HUMAN; INJURY; LIBIDO; LIVER FUNCTION TEST; LOW DRUG DOSE; MENSTRUATION; MENTAL STRESS; MYALGIA; MYOPATHY; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROPHYLAXIS; PROTEIN FUNCTION; SIDE EFFECT; SWELLING;

6-AMINOCAPROIC ACID; ANDROGENS; ANGIOEDEMA, HEREDITARY; ANTIFIBRINOLYTIC AGENTS; BLOOD TRANSFUSION; HUMANS; PLASMA;

EID: 38649124663     PISSN: 00916749     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaci.2007.07.057     Document Type: Article

References (18)

1. Frank M.M. Hereditary angioedema: the clinical syndrome and its management in the United States. Immunol Allergy Clin North Am 26 (2006) 653-668
2. Frank M.M., Gelfand J.A., and Atkinson J.P. Hereditary angioedema: the clinical syndrome and its management. Ann Intern Med 84 (1976) 589-593
3. Agostoni A., Cicardi M., Cugno M., Zingale L.C., Gioffre D., and Nussberger J. Angioedema due to angiotensin-converting enzyme inhibitors. Immunopharmacology 44 (1999) 21-25
4. Frank M.M. Effect of sex hormones on the complement-related clinical disorder of hereditary angioedema. Arthritis Rheum 22 (1979) 1295-1299
5. Landerman N.S., Webster M.E., Becker E.L., and Ratcliffe H.E. Hereditary angioneurotic edema. J Allergy 33 (1962) 330-341
6. Donaldson V.H., and Evans R.R. A biochemical abnormality in hereditary angioneurotic edema. Am J Med 35 (1963) 37-44
7. Rosen F.S., Pensky J., Donaldson V., and Charache P. Hereditary angioneurotic edema: two genetic variants. Science 148 (1965) 957-958
8. Davis III A.E. Mechanism of angioedema in first complement component inhibitor deficiency. Immunol Allergy Clin North Am 26 (2006) 633-651
9. Brickman C.M., Tsoko G.C., Balow J.E., Lawley T.J., Hammer C.H., and Frank M.M. Immunoregulatory diseases associated with hereditary angioedema: 1. Clinical manifestations of autoimmune disease. J Allergy Clin Immunol 77 (1986) 749-757
10. Spaulding W.B. Methyltestosterone therapy for hereditary episodic edema (hereditary angioneurotic edema). Ann Intern Med 53 (1960) 739-745
11. Gelfand J.A., Sherins R.J., Alling D.W., and Frank M.M. Treatment of hereditary angioedema with danazol. N Engl J Med 295 (1976) 1444-1448
12. 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
13. Gadek J.E., Hosea S.W., Gelfand J.A., Santaella M., Wickerhauser M., Triantaphyllopoulos D.C., et al. Replacement therapy in hereditary angioedema. N Engl J Med 302 (1980) 542-546
14. Waytes A.T., Rosen F.S., and Frank M.M. Treatment of Hereditary Angioedema with a Vapor-Heated C1 Inh Concentrate. N Engl J Med 334 (1996) 1630-1634
15. Levi M., Choi G., Picavet C., and Hack C.E. Self-administration of C1-inhibitor concentrate in patients with hereditary or acquired angioedema caused by C1-inhibitor deficiency. J Allergy Clin Immunol 117 (2006) 904-908
16. Bowen T., Cicardi M., Farkas H., Bork K., Kreuz W., Zingale 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
17. Farkas H. Hereditary and acquired angioedema: problems and progress. Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond. J Allergy Clin Immunol 114 suppl (2004) S51-S131
18. Gompels M.M., Lock R.J., Abinun M., Bethune C.A., Davies G., Grattan C., et al. C1 Inh deficiency: consensus document. Clin Exp Immunol 139 (2005) 379-394