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

Year Number of Results
1966 1
1974 1
1979 1
1980 1
1982 1
1983 1
1984 2
1985 2
1987 1
1988 2
1989 4
1990 3
1991 2
1993 3
1996 1
1997 1
1998 3
1999 2
2000 2
2003 1
2004 1
2006 1
2007 6
2008 18
2009 9
2010 24
2011 32
2012 33
2013 33
2014 25
2015 28
2016 25
2017 16
2018 20
2019 34
2020 30
2021 30
2022 22
2023 17
2024 1

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399 results

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Page 1
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 increa
Angioedema as a systemic disease.
Kazandjieva J, Christoff G. Kazandjieva J, et al. Clin Dermatol. 2019 Nov-Dec;37(6):636-643. doi: 10.1016/j.clindermatol.2019.07.035. Epub 2019 Aug 1. Clin Dermatol. 2019. PMID: 31864442 Review.
Angioedema is a clinical entity defined as self-limiting edema localized in the deeper layers of the skin and mucosa and lasting for several days. ...Suspected cases need an accurate differential diagnosis to exclude all other types of acquired and hereditary angioe …
Angioedema is a clinical entity defined as self-limiting edema localized in the deeper layers of the skin and mucosa and lasting for …
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. ...Formally known as type III HAE is typically an estrogen-dependent or hereditary angioedema with normal C1-INH activity. Current guidelines now re
Hereditary angioedema (HAE) is an autosomal dominant disorder caused by a mutation in the C1 esterase inhibitor gene. ...Formally kno
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). ...
Hereditary angioedema (HAE) is an autosomal dominant disorder defined by a deficiency of functional C1 esterase inhibitor (C1-INH). .
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.
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. ...
Hereditary angioedema due to C1-esterase inhibitor deficiency (C1-INH-HAE) is a rare autosomal dominant disease. ...
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 histaminergic a …
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 potential
Abdominal Pain Mimics.
Murali N, El Hayek SM. Murali N, et al. Emerg Med Clin North Am. 2021 Nov;39(4):839-850. doi: 10.1016/j.emc.2021.07.003. Epub 2021 Sep 10. Emerg Med Clin North Am. 2021. PMID: 34600641 Free PMC article. Review.
SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes.
Ponard D, Gaboriaud C, Charignon D, Ghannam A, Wagenaar-Bos IGA, Roem D, López-Lera A, López-Trascasa M, Tosi M, Drouet C. Ponard D, et al. Hum Mutat. 2020 Jan;41(1):38-57. doi: 10.1002/humu.23917. Epub 2019 Oct 22. Hum Mutat. 2020. PMID: 31517426 Free article. Review.
C1 inhibitor (C1Inh) deficiency is responsible for hereditary angioedema (C1-INH-HAE) and caused by variants of the SERPING1/C1INH/C1NH gene. ...
C1 inhibitor (C1Inh) deficiency is responsible for hereditary angioedema (C1-INH-HAE) and caused by variants of the SERPING1/C1INH/C1 …
399 results