Literature DB >> 27037399

Hereditary angioedema with F12 mutation: first report of three cases associated with immune disorders.

Irène Gallais Sérézal1, Robin Dhôte2, Frédéric Caux3, Arséne Mèkinian4, Olivier Fain4.   

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Year:  2016        PMID： 27037399      PMCID： PMC4952983          DOI： 10.7861/clinmedicine.16-2-206

Source DB:  PubMed          Journal:  Clin Med (Lond)        ISSN： 1470-2118            Impact factor:   2.659


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  4 in total

1.  Lack of increased prevalence of immunoregulatory disorders in hereditary angioedema due to C1-inhibitor deficiency.

Authors:  Henriette Farkas; Dorottya Csuka; Judit Gács; Ibolya Czaller; Zsuzsanna Zotter; George Füst; Lilian Varga; Péter Gergely
Journal:  Clin Immunol       Date:  2011-05-19       Impact factor: 3.969

Review 2.  Cutaneous manifestations of complement deficiencies.

Authors:  D Lipsker; G Hauptmann
Journal:  Lupus       Date:  2010-08       Impact factor: 2.911

3.  Hereditary angioedema caused by missense mutations in the factor XII gene: clinical features, trigger factors, and therapy.

Authors:  Konrad Bork; Karin Wulff; Jochen Hardt; Günther Witzke; Petra Staubach
Journal:  J Allergy Clin Immunol       Date:  2009-05-27       Impact factor: 10.793

4.  Hereditary and acquired C1-inhibitor deficiency: biological and clinical characteristics in 235 patients.

Authors:  A Agostoni; M Cicardi
Journal:  Medicine (Baltimore)       Date:  1992-07       Impact factor: 1.889
  4 in total

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