Medical Literature - 1969

Hereditary angio-oedema treated with E-aminocaproic acid

Champion RH, Lachmann PJ. 10/1969 British Journal of Dermatology

SUMMARY.— Two brothers with hereditary angio-oedema have been studied, the only 2 cases among 227 patients with angio-oedema seen in 10 years. The absence of the inhibitor of the activated first component of complement in their serum confirmed the diagnosis. In a double blind trial their symptoms were partially controlled by ε – aminocaproic acid, although there were no consistent changes in the serum complement levels.

Available online at: onlinelibrary.wiley.com/doi/10.1111/j.1365-2133.1969.tb15938.x/abstract (small fee)

Treatment of familial angio-oedema

Owen RM. 3/1969 Lancet

Available online at: sciencedirect.com/science/article/pii/S0140673669919862 (small fee)

Use of a kallikrein inhibitor in the treatment of urticaria and hereditary angioneurotic edema

Juhlin L, Michaelsson G. 1/1969 Acta Dermato Venereologica

Volume 49(1): pages: 37-44

Not available online.

Vascular reactions in hereditary angioneurotic edema

Juhlin L, Michaelsson G. 1/1969 Acta Dermato Venereologica

Issue: 49(1): pages: 20-25.

Not available online.

Funding for Canadian Hereditary Angioedema Network has been generously provided by unrestricted grants from:

BioCryst

CSL Behring

Takeda

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