Literature DB >> 29952006

Plasminogen gene mutation with normal C1 inhibitor hereditary angioedema: Three additional French families.

Aude Belbézier1, Gaelle Hardy2,3, Raphael Marlu2,4, Federica Defendi2,5, Chantal Dumestre Perard2,5, Isabelle Boccon-Gibod1,2, David Launay2,6, Laurence Bouillet1,2.   

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Year:  2018        PMID： 29952006     DOI： 10.1111/all.13543

Source DB:  PubMed          Journal:  Allergy        ISSN： 0105-4538            Impact factor:   13.146


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  12 in total

Review 1.  Leveraging Genetics for Hereditary Angioedema: A Road Map to Precision Medicine.

Authors:  Anastasios E Germenis; Matija Rijavec; Camila Lopes Veronez
Journal:  Clin Rev Allergy Immunol       Date:  2021-01-28       Impact factor: 8.667

Review 2.  Pathophysiology of Hereditary Angioedema (HAE) Beyond the SERPING1 Gene.

Authors:  Jyoti Sharma; Ankur Kumar Jindal; Aaqib Zaffar Banday; Anit Kaur; Amit Rawat; Surjit Singh; Hilary Longhurst
Journal:  Clin Rev Allergy Immunol       Date:  2021-01-14       Impact factor: 8.667

3.  Genotype-first analysis of a generally healthy population cohort supports genetic testing for diagnosis of hereditary angioedema of unknown cause.

Authors:  Dale L Bodian; Thierry Vilboux; Natalie S Hauser
Journal:  Allergy Asthma Clin Immunol       Date:  2019-05-16       Impact factor: 3.406

Review 4.  Bradykinin-Mediated Angioedema: An Update of the Genetic Causes and the Impact of Genomics.

Authors:  Itahisa Marcelino-Rodriguez; Ariel Callero; Alejandro Mendoza-Alvarez; Eva Perez-Rodriguez; Javier Barrios-Recio; Jose C Garcia-Robaina; Carlos Flores
Journal:  Front Genet       Date:  2019-09-27       Impact factor: 4.599

5.  Commentary: Bradykinin-Mediated Angioedema: An Update of the Genetic Causes and the Impact of Genomics.

Authors:  Roger Colobran
Journal:  Front Genet       Date:  2020-04-03       Impact factor: 4.599

6.  Screening for Plasminogen Mutations in Hereditary Angioedema Patients.

Authors:  Henriette Farkas; Anna Dóczy; Edina Szabó; Lilian Varga; Dorottya Csuka
Journal:  Genes (Basel)       Date:  2021-03-11       Impact factor: 4.096

7.  Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene.

Authors:  Konrad Bork; Karin Wulff; Guenther Witzke; Thomas Machnig; Jochen Hardt
Journal:  Orphanet J Rare Dis       Date:  2020-02-17       Impact factor: 4.123

Review 8.  The International/Canadian Hereditary Angioedema Guideline.

Authors:  Stephen Betschel; Jacquie Badiou; Karen Binkley; Rozita Borici-Mazi; Jacques Hébert; Amin Kanani; Paul Keith; Gina Lacuesta; Susan Waserman; Bill Yang; Emel Aygören-Pürsün; Jonathan Bernstein; Konrad Bork; Teresa Caballero; Marco Cicardi; Timothy Craig; Henriette Farkas; Anete Grumach; Connie Katelaris; Hilary Longhurst; Marc Riedl; Bruce Zuraw; Magdelena Berger; Jean-Nicolas Boursiquot; Henrik Boysen; Anthony Castaldo; Hugo Chapdelaine; Lori Connors; Lisa Fu; Dawn Goodyear; Alison Haynes; Palinder Kamra; Harold Kim; Kelly Lang-Robertson; Eric Leith; Christine McCusker; Bill Moote; Andrew O'Keefe; Ibraheem Othman; Man-Chiu Poon; Bruce Ritchie; Charles St-Pierre; Donald Stark; Ellie Tsai
Journal:  Allergy Asthma Clin Immunol       Date:  2019-11-25       Impact factor: 3.406

9.  The natural course of hereditary angioedema in a Chinese cohort.

Authors:  Yang Cao; Shuang Liu; Yuxiang Zhi
Journal:  Orphanet J Rare Dis       Date:  2020-09-22       Impact factor: 4.123

10.  Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence.

Authors:  Konrad Bork; Thomas Machnig; Karin Wulff; Guenther Witzke; Subhransu Prusty; Jochen Hardt
Journal:  Orphanet J Rare Dis       Date:  2020-10-15       Impact factor: 4.123
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