K Bork, K Wulff, P Meinke, N Wagner, J Hardt… - Clinical …, 2011 - Elsevier In hereditary angioedema with normal C1-inhibitor two different missense mutations of codon p.Thr328* in the coagulation factor 12 gene have been reported in some families. In this study a novel factor 12 gene mutation, the deletion of 72 base pairs (bp) (c.971_1018 + ...
L Bouillet, T Mannic, M Arboleas… - The Journal of allergy …, 2011 - ncbi.nlm.nih.gov Hereditary angioedema: Key role for kallikrein and bradykinin in vascular endothelial-cadherin cleavage and edema formation. ... Bouillet L, Mannic T, Arboleas M, Subileau M, Massot C, Drouet C, Huber P, Vilgrain I. ... INSERM U1036, CEA, Institute of Life Sciences Research and ... Related articles - All 2 versions
K Bork, J Hardt, P Staubach-Renz… - Oral surgery, oral …, 2011 - ncbi.nlm.nih.gov OBJECTIVE: Tooth extractions may trigger clinical symptoms of hereditary angioedema due to C1 inhibitor deficiency (HAE-C1-INH). The aim of this study was to determine how many tooth extractions were followed by symptoms of HAE-C1-INH in patients with and without ... All 3 versions
MA Riedl - Allergy and Asthma Proceedings, 2011 - ingentaconnect.com Hereditary angioedema (HAE) is a genetic autosomal dominant condition caused by C1-esterase inhibitor protein (C1INH) deficiency that results in episodic tissue angioedema. Recently, new therapies have been developed to more effectively manage this rare but serious ... All 2 versions
WR Lumry, P Busse, J Baker… - Journal of Allergy and …, 2011 - jacionline.org ... AB234, February 2011. Pre-procedure Administration of C1 Esterase Inhibitor (Human) (Cinryze™) for the Prevention of HereditaryAngioedema (HAE) Attacks after Medical, Dental, or Surgical Procedures. WR Lumry: Affiliations. ... Cached - All 2 versions