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7. 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 Clin Exp Immunol; 2016 Sep; 185(3):332-7. PubMed ID: 27271546 [TBL] [Abstract][Full Text] [Related]
8. 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 Clin Immunol; 2015 Apr; 157(2):239-48. PubMed ID: 25744496 [TBL] [Abstract][Full Text] [Related]
10. An ABC of the Warning Signs of Hereditary Angioedema. Grumach AS; Ferraroni N; Olivares MM; López-Serrano MC; Bygum A Int Arch Allergy Immunol; 2017; 174(1):1-6. PubMed ID: 28950264 [TBL] [Abstract][Full Text] [Related]
11. 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; Arruda LK Int Arch Allergy Immunol; 2015; 166(2):114-20. PubMed ID: 25790805 [TBL] [Abstract][Full Text] [Related]
12. Hereditary and acquired C1-inhibitor-dependent angioedema: from pathophysiology to treatment. Zeerleder S; Levi M Ann Med; 2016; 48(4):256-67. PubMed ID: 27018196 [TBL] [Abstract][Full Text] [Related]
15. Hereditary Angioedema with Normal C1 Inhibitor: Update on Evaluation and Treatment. Magerl M; Germenis AE; Maas C; Maurer M Immunol Allergy Clin North Am; 2017 Aug; 37(3):571-584. PubMed ID: 28687110 [TBL] [Abstract][Full Text] [Related]
16. 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 Orphanet J Rare Dis; 2020 Oct; 15(1):289. PubMed ID: 33059692 [TBL] [Abstract][Full Text] [Related]
17. 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; 12(4):257-68. PubMed ID: 20593909 [TBL] [Abstract][Full Text] [Related]
18. Clinical and biological response to rituximab treatment in 3 patients with acquired C1-inhibitor deficiency. Busse PJ; Gernez Y Ann Allergy Asthma Immunol; 2017 Oct; 119(4):380-382. PubMed ID: 28866304 [No Abstract] [Full Text] [Related]
19. The bradykinin-forming cascade and its role in hereditary angioedema. Kaplan AP; Joseph K Ann Allergy Asthma Immunol; 2010 Mar; 104(3):193-204. PubMed ID: 20377108 [TBL] [Abstract][Full Text] [Related]
20. Deficiency of plasminogen activator inhibitor 2 in plasma of patients with hereditary angioedema with normal C1 inhibitor levels. Joseph K; Tholanikunnel BG; Wolf B; Bork K; Kaplan AP J Allergy Clin Immunol; 2016 Jun; 137(6):1822-1829.e1. PubMed ID: 26395818 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]