Anette Bygum

Research interests

Publications

• Definition, acronyms, nomenclature, and classification of angioedema (DANCE): AAAAI, ACAAI, ACARE, and APAAACI DANCE consensus

  Journal of Allergy and Clinical Immunology · 2024 · 10.1016/j.jaci.2024.03.024

• The international WAO/EAACI guideline for the management of hereditary angioedema—The 2021 revision and update

  Allergy · 2022 · https://doi.org/10.1111/all.15214

• The international WAO/EAACI guideline for the management of hereditary angioedema – The 2021 revision and update

  World Allergy Organization Journal · 2022 · 10.1016/j.waojou.2022.100627

• The impact of lymphedema on health-related quality of life up to 10 years after breast cancer treatment

  npj Breast Cancer · 2021 · 10.1038/s41523-021-00276-y

• Oral Plasma Kallikrein Inhibitor for Prophylaxis in Hereditary Angioedema

  New England Journal of Medicine · 2018 · 10.1056/nejmoa1716995

• Management of congenital ichthyoses: European guidelines of care, part two

  British Journal of Dermatology · 2018 · 10.1111/bjd.16882

• Management of congenital ichthyoses: European guidelines of care, part one

  British Journal of Dermatology · 2018 · 10.1111/bjd.17203

• Henoch-Schönlein Purpura: A Literature Review

  Acta Dermato Venereologica · 2017 · https://doi.org/10.2340/00015555-2733

• Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting

  Annals of Allergy Asthma & Immunology · 2016 · 10.1016/j.anai.2016.08.014

• Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome

  The American Journal of Human Genetics · 2016 · 10.1016/j.ajhg.2016.10.004

• The Humanistic, Societal, and Pharmaco-economic Burden of Angioedema

  Clinical Reviews in Allergy & Immunology · 2016 · 10.1007/s12016-016-8575-2

• Burden of Illness in Hereditary Angioedema: A Conceptual Model

  Acta Dermato Venereologica · 2015 · 10.2340/00015555-2014

• Mutations in POGLUT1, Encoding Protein O-Glucosyltransferase 1, Cause Autosomal-Dominant Dowling-Degos Disease

  The American Journal of Human Genetics · 2014 · 10.1016/j.ajhg.2013.12.003

• Socioeconomic burden of hereditary angioedema: results from the hereditary angioedema burden of illness study in Europe

  Orphanet Journal of Rare Diseases · 2014 · 10.1186/1750-1172-9-99

• The humanistic burden of hereditary angioedema: Results from the Burden of Illness Study in Europe

  Allergy and Asthma Proceedings · 2013 · https://doi.org/10.2500/aap.2013.34.3685

• Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema

  Molecular Syndromology · 2013 · 10.1159/000354097

• International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency

  Journal of Allergy and Clinical Immunology · 2011 · https://doi.org/10.1016/j.jaci.2011.11.025

• 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema

  Allergy Asthma and Clinical Immunology · 2010 · https://doi.org/10.1186/1710-1492-6-24

• HAE international home therapy consensus document

  Allergy Asthma and Clinical Immunology · 2010 · 10.1186/1710-1492-6-22

• Genotypic and Clinical Spectrum of Self-Improving Collodion Ichthyosis: ALOX12B, ALOXE3, and TGM1 Mutations in Scandinavian Patients

  Journal of Investigative Dermatology · 2009 · 10.1038/jid.2009.346

• Self-administration of intravenous C1-inhibitor therapy for hereditary angioedema and associated quality of life benefits

  European Journal of Dermatology · 2009 · 10.1684/ejd.2008.0603

• Hereditary angio-oedema in Denmark: a nationwide survey

  British Journal of Dermatology · 2009 · https://doi.org/10.1111/j.1365-2133.2009.09366.x

• Benefits and risks of danazol in hereditary angioedema: a long-term survey of 118 patients

  Annals of Allergy Asthma & Immunology · 2008 · https://doi.org/10.1016/s1081-1206(10)60424-3

• Disease expression in women with hereditary angioedema

  American Journal of Obstetrics and Gynecology · 2008 · 10.1016/j.ajog.2008.04.034

• Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

  Nature Genetics · 2003 · 10.1038/ng1163

Current projects

No projects listed.