Anette Bygum - Concepedia

Author

Anette Bygum

Odense University Hospital ORCID

Also Known As

A Bygum, A. BYGUM, A. Bygum, A., Bygum, ANETTE BYGUM, Anette Bygum, Anette Bygum, Annette Bygum, Bygum A, Bygum, A.

479

Publications

9.7K

Citations

H-Index

141

Concepts

All Affiliations

Odense University Hospital University of Southern Denmark Semmelweis University Aarhus University Hospital Goethe University Frankfurt

About

Anette Bygum is an author at Odense University Hospital specializing in medicine, pathology, and autoimmune disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	30	55	3.6K
2	Public Health	5	5	556
3	Natural Sciences	4	4	180
4	Health Sciences	1	1	16
5	Nursing	1	1	162

Anette Bygum

128

Publications

7.6K

Citations

H-Index

Page 1

	Year	Citations
2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema Tom Bowen, Marco Cicardi, Henriette Farkas, Allergy Asthma and Clinical Immunology	2010	611
The international WAO/EAACI guideline for the management of hereditary angioedema—The 2021 revision and update Marcus Maurer, Markus Magerl, Stephen Betschel, Allergy ThrombosisType 1Cardiovascular DiseaseHereditary AngioedemaHematology	2022	441
International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency Teresa Caballero, Henriette Farkas, Laurence Bouillet, Journal of Allergy and Clinical Immunology Cardiovascular DiseaseC1 Inhibitor DeficiencyInternational ConsensusHematologyHereditary Angioedema	2011	250
Hereditary angio-oedema in Denmark: a nationwide survey Anette Bygum British Journal of Dermatology	2009	246
Benefits and risks of danazol in hereditary angioedema: a long-term survey of 118 patients Konrad Bork, Anette Bygum, Jochen Hardt Annals of Allergy Asthma & Immunology MedicineHereditary AngioedemaLong-term Survey	2008	224
The humanistic burden of hereditary angioedema: Results from the Burden of Illness Study in Europe Teresa Caballero, Emel Aygören‐Pürsün, Anette Bygum, Allergy and Asthma Proceedings	2013	204
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin Etgar Levy‐Nissenbaum, Regina C. Betz, Moshe Frydman, Nature Genetics Hypotrichosis SimplexGeneticsPathologyMolecular GeneticsNonsense Mutations	2003	174
Disease expression in women with hereditary angioedema Laurence Bouillet, Hilary Longhurst, Isabelle Boccon‐Gibod, American Journal of Obstetrics and Gynecology ThrombosisCardiovascular DiseaseVascular MalformationPathologyVascular Surgery	2008	173
HAE international home therapy consensus document Hilary Longhurst, Henriette Farkas, Timothy Craig, Allergy Asthma and Clinical Immunology NursingPrimary CareMedicineC1 Inhibitor DeficiencyHereditary Angioedema	2010	162
Mutations in POGLUT1, Encoding Protein O-Glucosyltransferase 1, Cause Autosomal-Dominant Dowling-Degos Disease F. Buket Basmanav, Ana‐Maria Oprişoreanu, Sandra M. Pasternack, The American Journal of Human Genetics Mendelian DisorderAutoimmune DiseaseDisease MechanismGenetic DisorderGenetics	2014	156

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