Hereditary angioedema with F12 mutation

Author:

Piñero-Saavedra Macarena,González-Quevedo Teresa,Saenz de San Pedro Blanca,Alcaraz Cristina,Bobadilla-González Pedro,Fernández-Vieira Lourdes,Hinojosa Belén,García-Lozano Raúl

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Immunology and Allergy,Immunology

Reference38 articles.

1. Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin, part I: classification, epidemiology, pathophysiology, genetics, clinical symptoms, and diagnosis;Caballero;J Investig Allergol Clin Immunol,2011

2. Recurrent angioedema: familial and oestrogen-induced;Warin;Br J Dermatol,1986

3. Hereditary angioedema with normal C1 inhibitor activity in women;Bork;Lancet,2000

4. Clinical, biochemical and genetic characterization of a novel estrogen-dependent inherited form of angioedema;Binkley;J Allergy Clin Immunol,2000

5. Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor;Dewald;Biochem Biophys Res Commun,2006

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1. Classification, Diagnosis, and Pathology of Angioedema Without Hives;Immunology and Allergy Clinics of North America;2024-08

2. Hereditary angioedema with normal C1-inhibitor;Annals of Allergy, Asthma & Immunology;2024-06

3. Angioedema With Normal Complement Studies: What Do We Know?;The Journal of Allergy and Clinical Immunology: In Practice;2023-08

4. Myoferline gene mutation сan be associated with recurrent angioedema;Russian Journal of Allergy;2023-07-09

5. Hereditary angioedema. Clinical guidelines. (D84.1);Russian Journal of Allergy;2021-06-26

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