Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema

Deficiency of plasminogen activator inhibitor 2 in plasma of patients with hereditary angioedema with normal C1 inhibitor levels

(2016) Kusumam Joseph et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Characterization of patients with angioedema without wheals: The importance of F12 gene screening

(2015) Davide Firinu et al.   CLINICAL IMMUNOLOGY

Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group

(2014) M. Cicardi et al.   ALLERGY

Hereditary angioedema with C1 inhibitor deficiency: clinical presentation and quality of life of 193 French patients

(2013) Laurence Bouillet et al.   ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY

Update on treatment of hereditary angioedema

(2013) Y.-Y. Xu et al.   CLINICAL AND EXPERIMENTAL ALLERGY

Novel duplication in the F12 gene in a patient with recurrent angioedema

(2013) Nóra Kiss et al.   CLINICAL IMMUNOLOGY

Benefits of progestin contraception in non-allergic angioedema

(2012) C. Saule et al.   CLINICAL AND EXPERIMENTAL ALLERGY

Evidence-based recommendations for the therapeutic management of angioedema owing to hereditary C1 inhibitor deficiency: consensus report of an International Working Group

(2011) M. Cicardi et al.   ALLERGY

Type III hereditary angio-oedema: clinical and biological features in a French cohort

(2010) V. Vitrat-Hincky et al.   ALLERGY

Missense mutation Thr309Lys in the coagulation factor XII gene in a Spanish family with hereditary angioedema type III

(2009) A. Prieto et al.   ALLERGY

Hereditary angioedema caused by missense mutations in the factor XII gene: Clinical features, trigger factors, and therapy

(2009) Konrad Bork et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Recurrent European missense mutation in the F12 gene in a British family with type III hereditary angioedema

(2009) Nikoletta Nagy et al.   JOURNAL OF DERMATOLOGICAL SCIENCE