The DOI matches its Crossref record; 48 of the 48 references it cites were found in a registry or an index.
Hereditary Angioedema
Abstract
Hereditary angioedema is a rare genetic disease that may include recurrent attacks of cutaneous angioedema, severe abdominal pain, and airway compromise. Prophylaxis and treatment include C1 inhibitor replacement and inhibition of the kallikrein and bradykinin pathways.
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Citations
Cites
A biochemical abnormality in hereditary angioneurotic edema
Donaldson, V. H., & Evans, R. R. (1963) · The American Journal of Medicine · doi:10.1016/0002-9343(63)90162-1 · Cited by 968
Zuraw, B. L. (2008) · New England Journal of Medicine · doi:10.1056/nejmcp0803977 · Cited by 693
Icatibant, a New Bradykinin-Receptor Antagonist, in Hereditary Angioedema
Cicardi, M., Banerji, A., Bracho, F., Malbrán, A., Rosenkranz, B., Riedl, M., Bork, K., Lumry, W., Aberer, W., Bier, H., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa0906393 · Cited by 564
Hereditary angioedema with normal C1-inhibitor activity in women
Bork, K., Barnstedt, S.-E., Koch, P., & Traupe, H. (2000) · The Lancet · doi:10.1016/s0140-6736(00)02483-1 · Cited by 557
Fatal laryngeal attacks and mortality in hereditary angioedema due to C1-INH deficiency
Bork, K., Hardt, J., & Witzke, G. (2012) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2012.05.055 · Cited by 456
Hereditary Angioneurotic Edema: Two Genetic Variants
Rosen, F. S., Charache, P., Pensky, J., & Donaldson, V. (1965) · Science · doi:10.1126/science.148.3672.957 · Cited by 437
Identification of prekallikrein and high-molecular-weight kininogen as a complex in human plasma.
Mandle, R. J., Colman, R. W., & Kaplan, A. P. (1976) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.73.11.4179 · Cited by 350
Ecallantide for the Treatment of Acute Attacks in Hereditary Angioedema
Cicardi, M., Levy, R. J., McNeil, D. L., Li, H. H., Sheffer, A. L., Campion, M., Horn, P. T., & Pullman, W. E. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa0905079 · Cited by 312
Banerji, A., Riedl, M. A., Bernstein, J. A., Cicardi, M., Longhurst, H. J., Zuraw, B. L., Busse, P. J., Anderson, J., Magerl, M., Martinez-Saguer, I., et al. (2018) · JAMA · doi:10.1001/jama.2018.16773 · Cited by 312
Self-citationHereditary angioedema with a mutation in the plasminogen gene
Bork, K., Wulff, K., Steinmüller‐Magin, L., Brænne, I., Staubach‐Renz, P., Witzke, G., & Hardt, J. (2018) · Allergy · doi:10.1111/all.13270 · Cited by 309
Cited by
The Expanding Spectrum of Mutations in Hereditary Angioedema
Veronez, C. L., Csuka, D., Sheikh, F. R., Zuraw, B. L., Farkas, H., & Bork, K. (2021) · The Journal of Allergy and Clinical Immunology: In Practice · doi:10.1016/j.jaip.2021.03.008 · Cited by 57
Metadata
- Authors
- Busse, P. J., & Christiansen, S. C.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2020-03-19
- Volume
- 382
- Issue
- 12
- Pages
- 1136-1148
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W4246423891
- Cited by
- 445
- References
- 48
- FWCI
- 25.36
- Type
- journal article
- Language
- en
- Open access
- closed
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- Busse, P. J., & Christiansen, S. C. (2020). Hereditary Angioedema. New England Journal of Medicine. https://doi.org/10.1056/nejmra1808012
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
