Similar articles for PMID: 27788882

Year	Number of Results
2006	1
2008	1
2009	5
2010	7
2011	8
2012	9
2013	7
2014	11
2015	12
2016	12
2017	13
2018	10
2019	4
2020	8
2021	9
2024	0

1

Hereditary angioedema with F12 mutation: Clinical features and enzyme polymorphisms in 9 Southwestern Spanish families.

Piñero-Saavedra M, González-Quevedo T, Saenz de San Pedro B, Alcaraz C, Bobadilla-González P, Fernández-Vieira L, Hinojosa B, García-Lozano R. Piñero-Saavedra M, et al. Ann Allergy Asthma Immunol. 2016 Nov;117(5):520-526. doi: 10.1016/j.anai.2016.09.001. Epub 2016 Oct 24. Ann Allergy Asthma Immunol. 2016. PMID: 27788882

2

Characterization of patients with angioedema without wheals: the importance of F12 gene screening.

Firinu D, Bafunno V, Vecchione G, Barca MP, Manconi PE, Santacroce R, Margaglione M, Del Giacco SR. Firinu D, et al. Clin Immunol. 2015 Apr;157(2):239-48. doi: 10.1016/j.clim.2015.02.013. Epub 2015 Mar 2. Clin Immunol. 2015. PMID: 25744496

3

Genetic analysis of Factor XII and bradykinin catabolic enzymes in a family with estrogen-dependent inherited angioedema.

Duan QL, Binkley K, Rouleau GA. Duan QL, et al. J Allergy Clin Immunol. 2009 Apr;123(4):906-10. doi: 10.1016/j.jaci.2008.12.010. J Allergy Clin Immunol. 2009. PMID: 19178938

4

Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families.

Veronez CL, Moreno AS, Constantino-Silva RN, Maia LSM, Ferriani MPL, Castro FFM, Valle SR, Nakamura VK, Cagini N, Gonçalves RF, Mansour E, Serpa FS, Coelho Dias GA, Piccirillo MA, Toledo E, de Souza Bernardes M, Cichon S, Stieber C, Arruda LK, Pesquero JB, Grumach AS. Veronez CL, et al. J Allergy Clin Immunol Pract. 2018 Jul-Aug;6(4):1209-1216.e8. doi: 10.1016/j.jaip.2017.09.025. Epub 2017 Nov 8. J Allergy Clin Immunol Pract. 2018. PMID: 29128335

5

Real-world cohort study of adult and pediatric patients treated for hereditary angioedema in the United States.

Tachdjian R, Johnson KE, Casso D, Oliveria SA, Devercelli G, Jain G. Tachdjian R, et al. Allergy Asthma Proc. 2020 May 1;41(3):172-182. doi: 10.2500/aap.2020.41.200011. Epub 2020 Mar 18. Allergy Asthma Proc. 2020. PMID: 32375961

6

Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema.

Deroux A, Boccon-Gibod I, Fain O, Pralong P, Ollivier Y, Pagnier A, Djenouhat K, Du-Thanh A, Gompel A, Faisant C, Launay D, Bouillet L. Deroux A, et al. Clin Exp Immunol. 2016 Sep;185(3):332-7. doi: 10.1111/cei.12820. Clin Exp Immunol. 2016. PMID: 27271546 Free PMC article.

7

Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence.

Bork K, Machnig T, Wulff K, Witzke G, Prusty S, Hardt J. Bork K, et al. Orphanet J Rare Dis. 2020 Oct 15;15(1):289. doi: 10.1186/s13023-020-01570-x. Orphanet J Rare Dis. 2020. PMID: 33059692 Free PMC article.

8

Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations.

Bork K, Wulff K, Witzke G, Hardt J. Bork K, et al. Allergy. 2015 Aug;70(8):1004-12. doi: 10.1111/all.12648. Epub 2015 May 22. Allergy. 2015. PMID: 25952149

9

[Hereditary angioedema].

Bouchard LJ, Hyry H, Meri S. Bouchard LJ, et al. Duodecim. 2012;128(24):2547-54. Duodecim. 2012. PMID: 23393928 Review. Finnish.

10

Coagulation Factor XII Gene Mutation in Brazilian Families with Hereditary Angioedema with Normal C1 Inhibitor.

Moreno AS, Valle SO, Levy S, França AT, Serpa FS, Arcuri HA, Palma MS, Campos WN, Dias MM, Ponard D, Monnier N, Lunardi J, Bork K, Silva WA Jr, Arruda LK. Moreno AS, et al. Int Arch Allergy Immunol. 2015;166(2):114-20. doi: 10.1159/000376547. Epub 2015 Mar 13. Int Arch Allergy Immunol. 2015. PMID: 25790805 Free article.

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