Literature DB >> 23265861

Less severe clinical manifestations in patients with hereditary angioedema with missense C1INH gene mutations.

Andras Bors, Dorottya Csuka, Lilian Varga, Henriette Farkas, Attila Tordai, George Füst, Agnes Szilagyi.   

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Year:  2012        PMID： 23265861     DOI： 10.1016/j.jaci.2012.11.015

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN： 0091-6749            Impact factor:   10.793


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  14 in total

1.  The FXII c.-4T>C Polymorphism as a Disease Modifier in Patients With Hereditary Angioedema Due to the FXII p.Thr328Lys Variant.

Authors:  Fernando Corvillo; María Eugenia de la Morena-Barrio; Carmen Marcos-Bravo; Margarita López-Trascasa; Vicente Vicente; Jonas Emsley; Teresa Caballero; Javier Corral; Alberto López-Lera
Journal:  Front Genet       Date:  2020-09-10       Impact factor: 4.599

Review 2.  Angioedema Phenotypes: Disease Expression and Classification.

Authors:  Maddalena Alessandra Wu; Francesca Perego; Andrea Zanichelli; Marco Cicardi
Journal:  Clin Rev Allergy Immunol       Date:  2016-10       Impact factor: 8.667

Review 3.  Genetics of Hereditary Angioedema Revisited.

Authors:  Anastasios E Germenis; Matthaios Speletas
Journal:  Clin Rev Allergy Immunol       Date:  2016-10       Impact factor: 8.667

4.  In Search of an Association Between Genotype and Phenotype in Hereditary Angioedema due to C1-INH Deficiency.

Authors:  David Loli-Ausejo; Alberto López-Lera; Christian Drouet; Marina Lluncor; Elsa Phillips-Anglés; María Pedrosa; Rosario Cabañas; Teresa Caballero
Journal:  Clin Rev Allergy Immunol       Date:  2021-01-19       Impact factor: 8.667

5.  The influence of trigger factors on hereditary angioedema due to C1-inhibitor deficiency.

Authors:  Zsuzsanna Zotter; Dorottya Csuka; Erika Szabó; Ibolya Czaller; Zsuzsanna Nébenführer; György Temesszentandrási; George Fust; Lilian Varga; Henriette Farkas
Journal:  Orphanet J Rare Dis       Date:  2014-03-28       Impact factor: 4.123

6.  Outcomes of long term treatments of type I hereditary angioedema in a Turkish family.

Authors:  Gulsen Akoglu; Belgin Kesim; Gokhan Yildiz; Ahmet Metin
Journal:  An Bras Dermatol       Date:  2017 Sep-Oct       Impact factor: 1.896

7.  An investigational RNAi therapeutic targeting Factor XII (ALN-F12) for the treatment of hereditary angioedema.

Authors:  Jingxuan Liu; June Qin; Anna Borodovsky; Timothy Racie; Adam Castoreno; Mark Schlegel; Martin A Maier; Tracy Zimmerman; Kevin Fitzgerald; James Butler; Akin Akinc
Journal:  RNA       Date:  2018-11-21       Impact factor: 4.942

8.  Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association.

Authors:  Slađana Andrejević; Peter Korošec; Mira Šilar; Mitja Košnik; Radovan Mijanović; Branka Bonači-Nikolić; Matija Rijavec
Journal:  PLoS One       Date:  2015-11-04       Impact factor: 3.240

Review 9.  The Genetics of Hereditary Angioedema: A Review.

Authors:  Rosa Santacroce; Giovanna D'Andrea; Angela Bruna Maffione; Maurizio Margaglione; Maria d'Apolito
Journal:  J Clin Med       Date:  2021-05-09       Impact factor: 4.241

Review 10.  Biomarkers in Hereditary Angioedema.

Authors:  Grzegorz Porebski; Mateusz Kwitniewski; Avner Reshef
Journal:  Clin Rev Allergy Immunol       Date:  2021-02-09       Impact factor: 8.667
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