Similar articles for PMID: 27037399

Year	Number of Results
2006	3
2007	1
2008	2
2009	9
2010	1
2011	9
2012	5
2013	7
2014	6
2015	8
2016	13
2017	13
2018	12
2019	10
2020	6
2021	1
2024	0

1

Hereditary angioedema with F12 mutation: first report of three cases associated with immune disorders.

Gallais Sérézal IR, Dhôte R, Caux F, Mèkinian A, Fain O. Gallais Sérézal IR, et al. Clin Med (Lond). 2016 Apr;16(2):206. doi: 10.7861/clinmedicine.16-2-206. Clin Med (Lond). 2016. PMID: 27037399 Free PMC article. No abstract available.

2

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.

3

Hereditary angioedema caused by the p.Thr309Lys mutation in the F12 gene: a multifactorial disease.

Gómez-Traseira C, López-Lera A, Drouet C, López-Trascasa M, Pérez-Fernández E, Favier B, Prior N, Caballero T. Gómez-Traseira C, et al. J Allergy Clin Immunol. 2013 Oct;132(4):986-9.e1-5. doi: 10.1016/j.jaci.2013.04.032. Epub 2013 Jul 10. J Allergy Clin Immunol. 2013. PMID: 23849223 No abstract available.

4

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

5

Recurrent European missense mutation in the F12 gene in a British family with type III hereditary angioedema.

Nagy N, Greaves MW, Tanaka A, McGrath JA, Grattan CE. Nagy N, et al. J Dermatol Sci. 2009 Oct;56(1):62-4. doi: 10.1016/j.jdermsci.2009.06.013. Epub 2009 Jul 31. J Dermatol Sci. 2009. PMID: 19647418 No abstract available.

6

A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor.

Bork K, Wulff K, Meinke P, Wagner N, Hardt J, Witzke G. Bork K, et al. Clin Immunol. 2011 Oct;141(1):31-5. doi: 10.1016/j.clim.2011.07.002. Epub 2011 Jul 30. Clin Immunol. 2011. PMID: 21849258

7

Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor.

Bork K, Wulff K, Hardt J, Witzke G, Lohse P. Bork K, et al. Haemophilia. 2014 Sep;20(5):e372-5. doi: 10.1111/hae.12519. Epub 2014 Aug 12. Haemophilia. 2014. PMID: 25113305 No abstract available.

8

SERPING1 and F12 combined variants in a hereditary angioedema family.

Charignon D, Ponard D, de Gennes C, Drouet C, Ghannam A. Charignon D, et al. Ann Allergy Asthma Immunol. 2018 Oct;121(4):500-502. doi: 10.1016/j.anai.2018.05.031. Epub 2018 Jun 6. Ann Allergy Asthma Immunol. 2018. PMID: 29885370 No abstract available.

9

Genetics of Hereditary Angioedema Revisited.

Germenis AE, Speletas M. Germenis AE, et al. Clin Rev Allergy Immunol. 2016 Oct;51(2):170-82. doi: 10.1007/s12016-016-8543-x. Clin Rev Allergy Immunol. 2016. PMID: 27116602 Review.

10

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

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