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

Author:

Farkas H.1,Martinez-Saguer I.2,Bork K.3,Bowen T.4,Craig T.5,Frank M.6,Germenis A. E.7,Grumach A. S.8,Luczay A.9,Varga L.1,Zanichelli A.10,

Affiliation:

1. 3rd Department of Internal Medicine; Hungarian Angioedema Center; Semmelweis University; Budapest Hungary

2. Hemophilia Center Rhine Main; Moerfelden-Walldorf Germany

3. Department of Dermatology; University Medical Center Mainz; Mainz Germany

4. Departments of Medicine and Paediatrics; University of Calgary; Calgary AB Canada

5. Department of Medicine, Pediatrics and Graduate Studies; Penn State University; Hershey PA USA

6. Department of Pediatrics; Duke University Medical Center; Durham NC USA

7. Department of Immunology and Histocompatibility; School of Health Sciences; Faculty of Medicine; University of Thessaly; Larissa Greece

8. Outpatient Group of Recurrent Infections; Faculty of Medicine ABC; Santo Andre SP Brazil

9. 1st Department of Pediatrics; Semmelweis University; Budapest Hungary

10. Department of Biomedical and Clinical Sciences “Luigi Sacco”; University of Milan, ASST Fatebenefratelli Sacco; Milan Italy

Funder

Biocryst

CSL Behring

Dyax

Pharming NV

Shire

Swedish Orphan Biovitrum

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

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1. Current and Emerging Therapeutics in Hereditary Angioedema;Immunology and Allergy Clinics of North America;2024-08

2. Normalization of C1 Inhibitor in a Patient with Hereditary Angioedema;New England Journal of Medicine;2024-07-04

3. The Burden of Hereditary Angioedema in a Large Family in Brazil;International Archives of Allergy and Immunology;2024-07-04

4. Experience of lanadelumab usage for long-term prophylaxis of attacks in hereditary angioedema in patients of the Moscow region;Russian Journal of Allergy;2024-06-16

5. Tumid lupus erythematosus in C1-inhibitor deficiency;Journal of the Royal College of Physicians of Edinburgh;2024-05-16

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