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Items: 1 to 20 of 215

1.

Inhibition of vascular permeability by antisense-mediated inhibition of plasma kallikrein and coagulation factor 12.

Bhattacharjee G, Revenko AS, Crosby JR, May C, Gao D, Zhao C, Monia BP, MacLeod AR.

Nucleic Acid Ther. 2013 Jun;23(3):175-87. doi: 10.1089/nat.2013.0417. Epub 2013 Apr 12.

PMID:
23582057
2.

Pathogenic mechanisms of bradykinin mediated diseases: dysregulation of an innate inflammatory pathway.

Kaplan AP, Joseph K.

Adv Immunol. 2014;121:41-89. doi: 10.1016/B978-0-12-800100-4.00002-7. Review.

PMID:
24388213
3.

C1-inhibitor polymers activate the FXII-dependent kallikrein-kinin system: Implication for a role in hereditary angioedema.

Madsen DE, Sidelmann JJ, Biltoft D, Gram J, Hansen S.

Biochim Biophys Acta. 2015 Jun;1850(6):1336-42. doi: 10.1016/j.bbagen.2015.03.005. Epub 2015 Mar 20.

PMID:
25800206
4.

Factor XII-independent activation of the bradykinin-forming cascade: Implications for the pathogenesis of hereditary angioedema types I and II.

Joseph K, Tholanikunnel BG, Bygum A, Ghebrehiwet B, Kaplan AP.

J Allergy Clin Immunol. 2013 Aug;132(2):470-5. doi: 10.1016/j.jaci.2013.03.026. Epub 2013 May 11.

PMID:
23672780
5.

The bradykinin-forming cascade and its role in hereditary angioedema.

Kaplan AP, Joseph K.

Ann Allergy Asthma Immunol. 2010 Mar;104(3):193-204. doi: 10.1016/j.anai.2010.01.007. Review.

PMID:
20377108
6.

Complement, Kinins, and Hereditary Angioedema: Mechanisms of Plasma Instability when C1 Inhibitor is Absent.

Kaplan AP, Joseph K.

Clin Rev Allergy Immunol. 2016 Oct;51(2):207-15. doi: 10.1007/s12016-016-8555-6. Review.

PMID:
27273087
7.

A Decade of Change: Recent Developments in Pharmacotherapy of Hereditary Angioedema (HAE).

Bork K.

Clin Rev Allergy Immunol. 2016 Oct;51(2):183-92. doi: 10.1007/s12016-016-8544-9. Review.

PMID:
27207174
8.

Bradykinin-mediated diseases.

Kaplan AP.

Chem Immunol Allergy. 2014;100:140-7. doi: 10.1159/000358619. Epub 2014 May 22. Review.

PMID:
24925394
9.

Current treatment of hereditary angioedema: An update on clinical studies.

Banerji A.

Allergy Asthma Proc. 2010 Sep-Oct;31(5):398-406. doi: 10.2500/aap.2010.31.3387. Review.

PMID:
20929607
10.

Recent advances in the management of hereditary angioedema.

Hemperly SE, Agarwal NS, Xu YY, Zhi YX, Craig TJ.

J Am Osteopath Assoc. 2013 Jul;113(7):546-55. doi: 10.7556/jaoa.2013.006. Review.

PMID:
23843378
11.

High-molecular-weight kininogen cleavage correlates with disease states in the bradykinin-mediated angioedema due to hereditary C1-inhibitor deficiency.

Suffritti C, Zanichelli A, Maggioni L, Bonanni E, Cugno M, Cicardi M.

Clin Exp Allergy. 2014 Dec;44(12):1503-14. doi: 10.1111/cea.12293.

PMID:
24552232
12.

Hereditary angioedema in childhood: an approach to management.

Ebo DG, Verweij MM, De Knop KJ, Hagendorens MM, Bridts CH, De Clerck LS, Stevens WJ.

Paediatr Drugs. 2010 Aug 1;12(4):257-68. doi: 10.2165/11532590-000000000-00000. Review.

PMID:
20593909
13.

A novel assay to diagnose hereditary angioedema utilizing inhibition of bradykinin-forming enzymes.

Joseph K, Bains S, Tholanikunnel BG, Bygum A, Aabom A, Koch C, Farkas H, Varga L, Ghebrehiwet B, Kaplan AP.

Allergy. 2015 Jan;70(1):115-9. doi: 10.1111/all.12520. Epub 2014 Oct 15.

14.

Genetics of Hereditary Angioedema Revisited.

Germenis AE, Speletas M.

Clin Rev Allergy Immunol. 2016 Oct;51(2):170-82. doi: 10.1007/s12016-016-8543-x. Review.

PMID:
27116602
15.

Current treatment options for hereditary angioedema due to C1 inhibitor deficiency.

Wu MA, Zanichelli A, Mansi M, Cicardi M.

Expert Opin Pharmacother. 2016;17(1):27-40. doi: 10.1517/14656566.2016.1104300. Epub 2015 Oct 29. Review.

PMID:
26512744
16.

Hereditary and acquired C1-inhibitor-dependent angioedema: from pathophysiology to treatment.

Zeerleder S, Levi M.

Ann Med. 2016;48(4):256-67. doi: 10.3109/07853890.2016.1162909. Epub 2016 Mar 26. Review.

PMID:
27018196
17.

Pathogenesis and laboratory diagnosis of hereditary angioedema.

Zuraw BL, Christiansen SC.

Allergy Asthma Proc. 2009 Sep-Oct;30(5):487-92. doi: 10.2500/aap.2009.30.3277.

PMID:
19843402
18.

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

Moreno AS, Valle SO, Levy S, Fran├ža AT, Serpa FS, Arcuri HA, Palma MS, Campos WN, Dias MM, Ponard D, Monnier N, Lunardi J, Bork K, Silva WA Jr, Arruda LK.

Int Arch Allergy Immunol. 2015;166(2):114-20. doi: 10.1159/000376547. Epub 2015 Mar 13.

PMID:
25790805
19.

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

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

Allergy. 2015 Aug;70(8):1004-12. doi: 10.1111/all.12648. Epub 2015 May 22.

PMID:
25952149
20.

Update on therapeutic developments for hereditary angioedema.

Christiansen SC, Zuraw BL.

Allergy Asthma Proc. 2009 Sep-Oct;30(5):500-5. doi: 10.2500/aap.2009.30.3282. Review.

PMID:
19843404

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