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

Year Number of Results
1947 1
1948 1
1949 1
1955 1
1958 1
1961 1
1962 4
1964 3
1965 5
1966 4
1967 6
1968 6
1969 11
1970 11
1971 15
1972 21
1973 24
1974 18
1975 19
1976 27
1977 29
1978 25
1979 40
1980 37
1981 17
1982 24
1983 40
1984 30
1985 34
1986 27
1987 36
1988 23
1989 36
1990 31
1991 35
1992 26
1993 36
1994 23
1995 24
1996 24
1997 23
1998 29
1999 26
2000 33
2001 36
2002 37
2003 31
2004 38
2005 42
2006 46
2007 66
2008 77
2009 67
2010 130
2011 143
2012 150
2013 153
2014 169
2015 148
2016 161
2017 135
2018 162
2019 185
2020 206
2021 250
2022 200
2023 238
2024 77

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3,510 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. ...Formally known as type III HAE is typically an estrogen-dependent or hereditary angioedema with normal C1-INH activity. Current gui
Hereditary angioedema (HAE) is an autosomal dominant disorder caused by a mutation in the C1 esterase inhibitor gene. ...Forma
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 respiratory
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder that usual results from a decreased level of functio
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 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.
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 respiratory
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder that usual results from a decreased level of functio
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 screening test for types 1 and 2 is complement component C4, which is low to absent at times of angioedema and during qu
Hereditary angioedema (HAE) is an autosomal dominant disorder defined by a deficiency of functional C1 esterase inhibitor (C1-
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.
Hereditary angioedema again revisited.
Bellanti JA, Settipane RA. Bellanti JA, et al. Allergy Asthma Proc. 2021 Mar 1;42(2):105-107. doi: 10.2500/aap.2021.42.210009. Allergy Asthma Proc. 2021. PMID: 33685554 Free PMC article. No abstract available.
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. The treatment options for both acute episodes of HAE and LTP, used to minimize
Hereditary angioedema (HAE) is a rare disease characterized by sudden and often unprovoked episodes of swelling that can be po
[Hereditary angioedema].
Aygören-Pürsün E, Bork K. Aygören-Pürsün E, et al. Internist (Berl). 2019 Sep;60(9):987-995. doi: 10.1007/s00108-019-0644-1. Internist (Berl). 2019. PMID: 31363809 Review. German.
Hereditary angioedema (HAE) encompasses a heterogeneous group of diseases with similar phenotypes but different underlying genotypes. Specific clinical signs may point to HAE as opposed to histaminergic angioedema: the typical prolonged development of angi
Hereditary angioedema (HAE) encompasses a heterogeneous group of diseases with similar phenotypes but different underlying gen
3,510 results