Prophylaxis – Prof. Marcus Maurer

Hereditary Angioedema Caused By C1-Esterase Inhibitor Deficiency: A Literature-Based Analysis and Clinical Commentary on Prophylaxis Treatment Strategies

53.

Gower, R. G., Busse, P. J., Aygören-Pürsün, E., Barakat, A. J., Caballero, T., Davis-Lorton, M., Farkas, H., Hurewitz, D. S., Jacobs, J. S., Johnston, D. T., Lumry, W., and Maurer, M.: Hereditary angioedema caused by C1-Esterase inhibitor deficiency: a literature-based analysis and clinical commentary on prophylaxis treatment strategies. World Allergy Organ. J. 2011: 4; S9-S21. IF: N/A

Long-term prophylaxis of hereditary angioedema with androgen derivates: a critical appraisal and potential alternatives

51.	Maurer, M. and Magerl, M.: Long-term prophylaxis of hereditary angioedema with androgen derivates: a critical appraisal and potential alternatives. J. Dtsch. Dermatol. Ges. 2011: 9; 99-107. IF: 1.47

Hereditary angioedema: an update on available therapeutic options

45.	Maurer, M. and Magerl, M.: Hereditary angioedema: an update on available therapeutic options. J. Dtsch. Dermatol. Ges. 2010: 8; 663-672. IF: 1.48

Evaluation of avoralstat, an oral kallikrein inhibitor, in a phase 3 hereditary angioedema prophylaxis trial: the OPuS-2 study

326	Riedl, M.+, Farkas, H., Bernstein, J. A., Bouillet, L., Sheridan, W. P., and Maurer, M.: Evaluation of avoralstat, an oral kallikrein inhibitor, in a phase 3 hereditary angioedema prophylaxis trial: the OPuS-2 study. Allergy 2018: 73; 1871-1880. IF: 6.77

Guideline: Hereditary angioedema due to C1 inhibitor deficiency. S1-Guideline of the German Society for Angioedema (DGA), German Society for Internal Medicine (DGIM), German Society for Otorhinolaryngology (DGHNO), German Society for Allergology and Clinical Immunology (DGAKI), German Society for Child and Adolescent Medicine (DGKJ), German Dermatological Society (DDG), German Society for Pediatric Allergology and Environmental Medicine (GPA), German Association of ENT Surgeons (BVHNO) and the German HAE Patient Association (HAE-SHG)

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Bork, K.+, Aygören-Pürsün, E., Bas, M., Biedermann, T., Greve, J., Hartmann, K., Magerl, M., Martinez-Saguer, I., Maurer, M., Ott, H., Schauf, L., Staubach, P., and Wedi, B.: Guideline: Hereditary angioedema due to C1 inhibitor deficiency. S1-Guideline of the German Society for Angioedema (DGA), German Society for Internal Medicine (DGIM), German Society for Otorhinolaryngology (DGHNO), German Society for Allergology and Clinical Immunology (DGAKI), German Society for Child and Adolescent Medicine (DGKJ), German Dermatological Society (DDG), German Society for Pediatric Allergology and Environmental Medicine (GPA), German Association of ENT Surgeons (BVHNO) and the German HAE Patient Association (HAE-SHG). Allergo J. Int. 2019: 28; 16-29. IF: 2.06

The international WAO/EAACI guideline for the management of hereditary angioedema – the 2017 revision and update

308

Maurer, M.*+, Magerl, M.*, Ansotegui, I., Aygören-Pürsün, E., Betschel, S., Bork, K., Bowen, T., Balle Boysen, H., Farkas, H., Grumach, A., Hide, M., Katelaris, C., Lockey, R., Longhurst, H., Lumry, W., Martinez-Saguer, I., Moldovan, D., Nast, A., Pawankar, R., Potter, P., Riedl, M., Ritchie, B., Rosenwasser, L., Sánchez-Borges, M., Zhi, X., Zuraw, B., and Craig, T.: The international WAO/EAACI guideline for the management of hereditary angioedema – the 2017 revision and update. World Allergy Organ. J. 2018: 11; 5. IF: 3.68

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