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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1948 1
1949 1
1955 1
1958 1
1961 1
1962 2
1964 2
1965 3
1967 1
1968 1
1969 4
1970 1
1971 1
1972 6
1973 5
1974 7
1975 7
1976 10
1977 15
1978 15
1979 20
1980 20
1981 12
1982 16
1983 31
1984 20
1985 23
1986 21
1987 26
1988 20
1989 24
1990 19
1991 27
1992 22
1993 26
1994 15
1995 17
1996 20
1997 21
1998 24
1999 20
2000 35
2001 31
2002 29
2003 30
2004 30
2005 41
2006 44
2007 63
2008 77
2009 64
2010 126
2011 143
2012 146
2013 151
2014 165
2015 143
2016 158
2017 133
2018 162
2019 174
2020 204
2021 240
2022 197
2023 228
2024 71

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3,095 results

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Page 1
Hereditary Angioedema: Diagnosis, Clinical Implications, and Pathophysiology.
Sinnathamby ES, Issa PP, Roberts L, Norwood H, Malone K, Vemulapalli H, Ahmadzadeh S, Cornett EM, Shekoohi S, Kaye AD. Sinnathamby ES, et al. Adv Ther. 2023 Mar;40(3):814-827. doi: 10.1007/s12325-022-02401-0. Epub 2023 Jan 7. Adv Ther. 2023. PMID: 36609679 Free PMC article. Review.
Hereditary angioedema (HAE) is an autosomal dominant disorder caused by a mutation in the C1 esterase inhibitor gene. ...Type I and II HAE result from a mutation in the SERPING1 gene, which encodes C1-INH. Formally known as type III HAE i
Hereditary angioedema (HAE) is an autosomal dominant disorder caused by a mutation in the C1 esterase inhibit
Hereditary Angioedema.
Wilkerson RG, Moellman JJ. Wilkerson RG, et al. Immunol Allergy Clin North Am. 2023 Aug;43(3):533-552. doi: 10.1016/j.iac.2022.10.012. Immunol Allergy Clin North Am. 2023. PMID: 37394258 Review.
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder that usual results from a decreased level of functional C1-INH and clinically manifests with intermittent attacks of swelling of the subcutaneous tissue or submucosal layers of the resp
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder that usual results from a decreased level of functio
Hereditary Angioedema.
Busse PJ, Christiansen SC. Busse PJ, et al. N Engl J Med. 2020 Mar 19;382(12):1136-1148. doi: 10.1056/NEJMra1808012. N Engl J Med. 2020. PMID: 32187470 Review. No abstract available.
Hereditary Angioedema: A Review.
Zafra H. Zafra H. WMJ. 2022 Apr;121(1):48-53. WMJ. 2022. PMID: 35442579 Free article. Review.
Hereditary angioedema (HAE) is a rare and disabling disorder wherein there is excessive bradykinin production, with subsequent increased vascular permeability in the superficial tissues and gastrointestinal and respiratory mucosa. ...
Hereditary angioedema (HAE) is a rare and disabling disorder wherein there is excessive bradykinin production, with subsequent
Hereditary and acquired angioedema.
Patel G, Pongracic JA. Patel G, et al. Allergy Asthma Proc. 2019 Nov 1;40(6):441-445. doi: 10.2500/aap.2019.40.4267. Allergy Asthma Proc. 2019. PMID: 31690390 Review.
Hereditary angioedema (HAE) is an autosomal dominant disorder defined by a deficiency of functional C1 esterase inhibitor (C1-INH). ...The management of HAE has been transformed with the advent of disease-specific therapies. On-dem
Hereditary angioedema (HAE) is an autosomal dominant disorder defined by a deficiency of functional C1 estera
Treatment of Hereditary Angioedema.
Caballero T. Caballero T. J Investig Allergol Clin Immunol. 2021 Feb;31(1):1-16. doi: 10.18176/jiaci.0653. J Investig Allergol Clin Immunol. 2021. PMID: 33602658 Free article. Review.
Hereditary angioedema due to C1-esterase inhibitor deficiency (C1-INH-HAE) is a rare autosomal dominant disease. ...Purified plasma-derived human C1 esterase inhibitor concentrate is the treatment of choice for
Hereditary angioedema due to C1-esterase inhibitor deficiency (C1-INH-HAE) is a rare autoso
Hereditary angioedema revisited.
Bellanti JA, Settipane RA. Bellanti JA, et al. Allergy Asthma Proc. 2018 Sep 1;39(5):329-331. doi: 10.2500/aap.2018.39.4169. Allergy Asthma Proc. 2018. PMID: 30153885 Free PMC article. No abstract available.
Isolated angioedema: A review of classification and update on management.
Kesh S, Bernstein JA. Kesh S, et al. Ann Allergy Asthma Immunol. 2022 Dec;129(6):692-702. doi: 10.1016/j.anai.2022.08.003. Epub 2022 Aug 19. Ann Allergy Asthma Immunol. 2022. PMID: 35988876 Review.
RESULTS: Herein, a case-based approach is presented for discussing the major types of angioedema, including the following: hereditary angioedema types I and II and normal complement, acquired angioedema, angiotensin-converting enzyme-induced angioedema, and histamin …
RESULTS: Herein, a case-based approach is presented for discussing the major types of angioedema, including the following: hereditary
Hereditary Angioedema: A Review of the Current and Evolving Treatment Landscape.
Betschel SD, Banerji A, Busse PJ, Cohn DM, Magerl M. Betschel SD, et al. J Allergy Clin Immunol Pract. 2023 Aug;11(8):2315-2325. doi: 10.1016/j.jaip.2023.04.017. Epub 2023 Apr 26. J Allergy Clin Immunol Pract. 2023. PMID: 37116793 Review.
Hereditary angioedema (HAE) is a rare disease characterized by sudden and often unprovoked episodes of swelling that can be potentially life-threatening when it involves the upper airway. ...
Hereditary angioedema (HAE) is a rare disease characterized by sudden and often unprovoked episodes of swelling that can be po
Hereditary Angioedema.
Wilkerson RG, Moellman JJ. Wilkerson RG, et al. Emerg Med Clin North Am. 2022 Feb;40(1):99-118. doi: 10.1016/j.emc.2021.09.002. Epub 2021 Oct 29. Emerg Med Clin North Am. 2022. PMID: 34782094 Review.
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder that usual results from a decreased level of functional C1-INH and clinically manifests with intermittent attacks of swelling of the subcutaneous tissue or submucosal layers of the resp
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder that usual results from a decreased level of functio
3,095 results