Literature DB >> 25668899

Improving C1 inhibitor deficiency (type 1 and type 2 hereditary angioedema) in Latin America.

J Fabiani, S Oliveira Rodrigues Valle, M Olivares, S Nieto, E Hernández Landeros, A Ginaca, L Bezrodnik, E Nievas, M Oleastro, O M Barrera, A M Gallardo, A King, J Rodriguez Galindo, M J Ochoa Carabantes, T Craig, M Martinez Alfonso, C Montenegro, A Sevciovic Grumach.   

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Year:  2014        PMID： 25668899

Source DB:  PubMed          Journal:  J Investig Allergol Clin Immunol        ISSN： 1018-9068            Impact factor:   4.333


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  2 in total

1.  Hereditary angioedema with normal C1 inhibitor in a French cohort: Clinical characteristics and response to treatment with icatibant.

Authors:  Laurence Bouillet; Isabelle Boccon-Gibod; David Launay; Anne Gompel; Gisele Kanny; Vincent Fabien; Oliver Fain
Journal:  Immun Inflamm Dis       Date:  2017-01-11

2.  International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency.

Authors:  H Farkas; I Martinez-Saguer; K Bork; T Bowen; T Craig; M Frank; A E Germenis; A S Grumach; A Luczay; L Varga; A Zanichelli
Journal:  Allergy       Date:  2016-09-08       Impact factor: 13.146
  2 in total

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