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Duodecim; laaketieteellinen aikakauskirja, 2013
Hereditary angioedema (HAE) is a rare autosomal dominant disease characterized by episodic swelling of the face, extremities, larynx, gastrointestinal tract or genitals. Three different subtypes have been identified so far. Type I and II HAE are caused by mutations in the C1 inhibitor gene leading to decreased or dysfunctional C1 inhibitor ...
Laura J, Bouchard +2 more
openaire +1 more source
Hereditary angioedema (HAE) is a rare autosomal dominant disease characterized by episodic swelling of the face, extremities, larynx, gastrointestinal tract or genitals. Three different subtypes have been identified so far. Type I and II HAE are caused by mutations in the C1 inhibitor gene leading to decreased or dysfunctional C1 inhibitor ...
Laura J, Bouchard +2 more
openaire +1 more source
Inhibition of Prekallikrein for Hereditary Angioedema
New England Journal of Medicine, 2022Brenda F Baker +2 more
exaly

