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Results: 1 to 20 of 121

Similar articles for PubMed (Select 22920075)

1.

Clinical, biochemical, and genetic characterization of type III hereditary angioedema in 13 Northwest Spanish families.

Marcos C, López Lera A, Varela S, Liñares T, Alvarez-Eire MG, López-Trascasa M.

Ann Allergy Asthma Immunol. 2012 Sep;109(3):195-200.e2. doi: 10.1016/j.anai.2012.05.022. Epub 2012 Jun 27.

PMID:
22920075
2.
3.
4.

Antihistamine-resistant angioedema in women with negative family history: estrogens and F12 gene mutations.

Bork K, Wulff K, Witzke G, Stanger C, Lohse P, Hardt J.

Am J Med. 2013 Dec;126(12):1142.e9-14. doi: 10.1016/j.amjmed.2013.05.017.

PMID:
24262729
5.

Missense mutation Thr309Lys in the coagulation factor XII gene in a Spanish family with hereditary angioedema type III.

Prieto A, Tornero P, Rubio M, Fernández-Cruz E, Rodriguez-Sainz C.

Allergy. 2009 Feb;64(2):284-6. doi: 10.1111/j.1398-9995.2008.01764.x.

PMID:
19178407
6.

Hereditary angioedema type III (estrogen-dependent) report of three cases and literature review.

Miranda AR, Ue AP, Sabbag DV, Furlani Wde J, Souza PK, Rotta O.

An Bras Dermatol. 2013 Jul-Aug;88(4):578-84. doi: 10.1590/abd1806-4841.20131818. Review.

7.

Clinical, biochemical, and genetic characterization of a novel estrogen-dependent inherited form of angioedema.

Binkley KE, Davis A 3rd.

J Allergy Clin Immunol. 2000 Sep;106(3):546-50.

PMID:
10984376
8.

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.

Am J Hum Genet. 2006 Dec;79(6):1098-104. Epub 2006 Oct 18.

9.

Hereditary angioedema with normal C1 inhibitor.

Bork K.

Immunol Allergy Clin North Am. 2013 Nov;33(4):457-70. doi: 10.1016/j.iac.2013.07.002. Epub 2013 Sep 5. Review.

PMID:
24176211
10.

Hereditary angioedema caused by missense mutations in the factor XII gene: clinical features, trigger factors, and therapy.

Bork K, Wulff K, Hardt J, Witzke G, Staubach P.

J Allergy Clin Immunol. 2009 Jul;124(1):129-34. doi: 10.1016/j.jaci.2009.03.038. Epub 2009 May 27.

PMID:
19477491
11.

Hereditary angioedema with normal c1 inhibition.

Bork K.

Curr Allergy Asthma Rep. 2009 Jul;9(4):280-5.

PMID:
19656474
12.

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.

J Allergy Clin Immunol. 2007 Oct;120(4):975-7. Epub 2007 Sep 7. No abstract available.

PMID:
17825897
13.

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.

Clin Immunol. 2011 Oct;141(1):31-5. doi: 10.1016/j.clim.2011.07.002. Epub 2011 Jul 30.

PMID:
21849258
14.

Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course.

Bork K, Gül D, Hardt J, Dewald G.

Am J Med. 2007 Nov;120(11):987-92.

PMID:
17976427
15.

A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family.

Ferraro MF, Moreno AS, Castelli EC, Donadi EA, Palma MS, Arcuri HA, Lange AP, Bork K, Sarti W, Arruda LK.

Allergy. 2011 Oct;66(10):1384-90. doi: 10.1111/j.1398-9995.2011.02658.x. Epub 2011 May 30.

PMID:
21623829
16.

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.

J Allergy Clin Immunol. 2013 Oct;132(4):986-9.e1-5. doi: 10.1016/j.jaci.2013.04.032. Epub 2013 Jul 10. No abstract available.

PMID:
23849223
17.

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.

Haemophilia. 2014 Sep;20(5):e372-5. doi: 10.1111/hae.12519. Epub 2014 Aug 12. No abstract available.

PMID:
25113305
18.

HAE update: special considerations in the female patient with hereditary angioedema.

Geng B, Riedl MA.

Allergy Asthma Proc. 2013 Jan-Feb;34(1):13-8. doi: 10.2500/aap.2013.34.3635. Review.

PMID:
23406930
19.

Novel duplication in the F12 gene in a patient with recurrent angioedema.

Kiss N, Barabás E, Várnai K, Halász A, Varga LÁ, Prohászka Z, Farkas H, Szilágyi Á.

Clin Immunol. 2013 Oct;149(1):142-5. doi: 10.1016/j.clim.2013.08.001. Epub 2013 Aug 9.

PMID:
23994767
20.

Type I hereditary angioedema in Taiwan -- clinical, biological features and genetic study.

Lei WT, Shyur SD, Huang LH, Kao YH, Lo CY.

Asian Pac J Allergy Immunol. 2011 Dec;29(4):327-31.

PMID:
22299312
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