Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families
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Published:2018-07
Issue:4
Volume:6
Page:1209-1216.e8
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ISSN:2213-2198
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Container-title:The Journal of Allergy and Clinical Immunology: In Practice
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language:en
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Short-container-title:The Journal of Allergy and Clinical Immunology: In Practice
Author:
Veronez Camila Lopes, Moreno Adriana S., Constantino-Silva Rosemeire Navickas, Maia Luana S.M., Ferriani Mariana P.L., Castro Fábio F.M., Valle Solange Rodrigues, Nakamura Victor Koji, Cagini Nathália, Gonçalves Rozana Fátima, Mansour Eli, Serpa Faradiba Sarquis, Coelho Dias Gabriela Andrade, Piccirillo Miguel Alberto, Toledo Eliana, de Souza Bernardes Marli, Cichon SvenORCID, Stieber Christiane, Arruda L. Karla, Pesquero João Bosco, Grumach Anete Sevciovic
Subject
Immunology and Allergy
Reference47 articles.
1. Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group;Cicardi;Allergy,2014 2. Hereditary angioedema with normal C1-inhibitor activity in women;Bork;Lancet,2000 3. Clinical, biochemical, and genetic characterization of a novel estrogen-dependent inherited form of angioedema;Binkley;J Allergy Clin Immunol,2000 4. Hereditary angioedema caused by missense mutations in the factor XII gene: clinical features, trigger factors, and therapy;Bork;J Allergy Clin Immunol,2009 5. Type III hereditary angio-oedema: clinical and biological features in a French cohort;Vitrat-Hincky;Allergy,2010
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