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Molecular Immunology|July 1, 2008
Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: functional and structural correlatesEmanuela Pappalardo, Sonia Caccia, Chiara Suffritti, et al.
Allergy and Asthma Proceedings|September 15, 2017
Recombinant human C1 esterase inhibitor for acute hereditary angioedema attacks with upper airway involvementMarc A Riedl, H Henry Li, Marco Cicardi, et al.
Allergy and Asthma Proceedings|February 15, 2013
Ecallantide for treatment of acute attacks of acquired C1 esterase inhibitor deficiencyNisha S Patel, Shirley M Fung, Andrea Zanichelli, et al.
Haematologica|May 10, 2007
Lymphoproliferative disease and acquired C1 inhibitor deficiencyRoberto Castelli, Daniela Lambertenghi Deliliers, Lorenza C Zingale, et al.
The Patient|April 3, 2012
Content validity of visual analog scales to assess symptom severity of acute angioedema attacks in adults with hereditary angioedema: an interview studyCarolyn Vivienne McMillan, Jane Speight, Anurag Relan, et al.
Immunobiology|October 25, 2002
Mechanisms of C1-inhibitor deficiencyEmanuela Pappalardo, Lorenza C Zingale, Adelaide Terlizzi, et al.
Clinical and Diagnostic Laboratory Immunology|August 9, 2005
Prevalence and clinical significance of immunoglobulin A antibodies against tissue transglutaminase in patients with diverse chronic liver diseasesAnastasios E Germenis, Efthalia E Yiannaki, Kalliopi Zachou, et al.
BMJ Open|October 9, 2017
Fabry disease due to D313Y and novel GLA mutationsKonstantinos Koulousios, Konstantinos Stylianou, Panagiotis Pateinakis, et al.
Anesthesia and Analgesia|February 27, 2020
Perioperative Management of Patients With Hereditary Angioedema With Special Considerations for Cardiopulmonary BypassKenichi A Tanaka, Samhati Mondal, Yoshihisa Morita, et al.
Cytokine|May 28, 2018
The role of the NLRP3 inflammasome and the activation of IL-1β in the pathogenesis of chronic viral hepatic inflammationAdam Molyvdas, Urania Georgopoulou, Nikolaos Lazaridis, et al.
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