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Intensive Care Medicine
Published in: Intensive Care Medicine 7/2011

01-07-2011 | Correspondence

One hypovolaemic shock…two kinin pathway abnormalities

Authors: Céline Guichon, Bernard Floccard, Brigitte Coppéré, Etienne Hautin, Florence Bagès-Limoges, Olivier Rouvière, Nicole Monnier, Christian Drouet, Bernard Allaouchiche

Published in: Intensive Care Medicine | Issue 7/2011

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Excerpt

Dear Editor, …
Literature
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Bork K, Staubach P, Eckardt AJ, Hardt J (2006) Symptoms, course, and complications of abdominal attacks in hereditary angioedema due to C1 inhibitor deficiency. Am J Gastroenterol 101:619–627PubMedCrossRef
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Bork K, Wulff K, Hardt J, Witzke G, Staubach P (2009) Hereditary angioedema caused by missense mutations in the factor XII gene: clinical features, trigger factors, and therapy. J Allergy Clin Immunol 124:129–134PubMedCrossRef
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Cichon S, Martin L, Hennies HC, Müller F, Van Driessche K, Karpushova A, Stevens W, Colombo R, Renné T, Drouet C, Bork K, Nöthen MM (2006) Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III. Am J Hum Genet 79:1098–1104PubMedCrossRef
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Bouillet L, Boccon-Gibod I, Ponard D, Drouet C, Cesbron JY, Dumestre-Perard C, Monnier N, Lunardi J, Massot C, Gompel A (2009) Bradykinin receptor 2 antagonist (icatibant) for hereditary angioedema type III attacks. Ann Allergy Asthma Immunol 103:448PubMedCrossRef
Metadata
Title
One hypovolaemic shock…two kinin pathway abnormalities
Authors
Céline Guichon
Bernard Floccard
Brigitte Coppéré
Etienne Hautin
Florence Bagès-Limoges
Olivier Rouvière
Nicole Monnier
Christian Drouet
Bernard Allaouchiche
Publication date
01-07-2011
Publisher
Springer-Verlag
Published in
Intensive Care Medicine / Issue 7/2011
Print ISSN: 0342-4642
Electronic ISSN: 1432-1238
DOI
https://doi.org/10.1007/s00134-011-2225-1

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