Drouet C - Search Results

1

Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III.

Björkqvist J, de Maat S, Lewandrowski U, Di Gennaro A, Oschatz C, Schönig K, Nöthen MM, Drouet C, Braley H, Nolte MW, Sickmann A, Panousis C, Maas C, Renné T. Björkqvist J, et al. Among authors: drouet c. J Clin Invest. 2015 Aug 3;125(8):3132-46. doi: 10.1172/JCI77139. Epub 2015 Jul 20. J Clin Invest. 2015. PMID: 26193639 Free PMC article.

2

Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III.

Cichon S, Martin L, Hennies HC, Müller F, Van Driessche K, Karpushova A, Stevens W, Colombo R, Renné T, Drouet C, Bork K, Nöthen MM. Cichon S, et al. Among authors: drouet c. Am J Hum Genet. 2006 Dec;79(6):1098-104. doi: 10.1086/509899. Epub 2006 Oct 18. Am J Hum Genet. 2006. PMID: 17186468 Free PMC article.

3

Hereditary angioedema with normal C1 inhibitor gene in a family with affected women and men is associated with the p.Thr328Lys mutation in the F12 gene.

Martin L, Raison-Peyron N, Nöthen MM, Cichon S, Drouet C. Martin L, et al. Among authors: drouet c. J Allergy Clin Immunol. 2007 Oct;120(4):975-7. doi: 10.1016/j.jaci.2007.07.002. Epub 2007 Sep 7. J Allergy Clin Immunol. 2007. PMID: 17825897 No abstract available.

4

Urticaria as a Presenting Prodromal Manifestation of Attacks of Hereditary Angioedema.

Martin L, Renné T, Drouet C. Martin L, et al. Among authors: drouet c. Acta Derm Venereol. 2016 May;96(4):574-5. doi: 10.2340/00015555-2350. Acta Derm Venereol. 2016. PMID: 26803996 Free article. No abstract available.

5

Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE-PLG patients.

Parsopoulou F, Charignon D, Tengo M, Psarros F, Maas C, Gonzalez-Quevedo T, Drouet C, Germenis AE, Ghannam A. Parsopoulou F, et al. Among authors: drouet c. Allergy. 2020 Aug;75(8):2099-2102. doi: 10.1111/all.14280. Epub 2020 Apr 6. Allergy. 2020. PMID: 32181895 No abstract available.

6

Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.

Charignon D, Ghannam A, Defendi F, Ponard D, Monnier N, López Trascasa M, Launay D, Caballero T, Djenouhat K, Fain O, Cichon S, Martin L, Drouet C. Charignon D, et al. Among authors: drouet c. Allergy. 2014 Dec;69(12):1659-65. doi: 10.1111/all.12515. Epub 2014 Oct 10. Allergy. 2014. PMID: 25134986

7

Angioedema attacks in patients with hereditary angioedema: Local manifestations of a systemic activation process.

Hofman ZL, Relan A, Zeerleder S, Drouet C, Zuraw B, Hack CE. Hofman ZL, et al. Among authors: drouet c. J Allergy Clin Immunol. 2016 Aug;138(2):359-66. doi: 10.1016/j.jaci.2016.02.041. Epub 2016 May 28. J Allergy Clin Immunol. 2016. PMID: 27246526 Review.

8

Presence of C1-inhibitor polymers in a subset of patients suffering from hereditary angioedema.

Madsen DE, Hansen S, Gram J, Bygum A, Drouet C, Sidelmann JJ. Madsen DE, et al. Among authors: drouet c. PLoS One. 2014 Nov 4;9(11):e112051. doi: 10.1371/journal.pone.0112051. eCollection 2014. PLoS One. 2014. PMID: 25369003 Free PMC article.

9

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. Among authors: drouet c. 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.

10

Recessive SERPING1 Variant Leads to Kinin-Kallikrein System Control Failure in a Consanguineous Brazilian Family with Hereditary Angioedema.

Maia LSM, Burger B, Ghannam A, Nunes FL, Ferriani MPL, Dias MM, Arruda LK, Drouet C, Cichon S. Maia LSM, et al. Among authors: drouet c. J Clin Med. 2023 Nov 24;12(23):7299. doi: 10.3390/jcm12237299. J Clin Med. 2023. PMID: 38068351 Free PMC article.

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