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Journal Abstract Search

763 related items for PubMed ID: 28687110

  • 1. 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
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  • 2. Hereditary angioedema with normal C1 inhibitor: clinical characteristics and treatment response with plasma-derived human C1 inhibitor concentrate (Berinert®) in a French cohort.
    Bouillet L, Boccon-Gibod I, Gompel A, Floccard B, Martin L, Blanchard-Delaunay C, Launay D, Fain O.
    Eur J Dermatol; 2017 Apr 01; 27(2):155-159. PubMed ID: 28251901
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  • 3. Plasmin is a natural trigger for bradykinin production in patients with hereditary angioedema with factor XII mutations.
    de Maat S, Björkqvist J, Suffritti C, Wiesenekker CP, Nagtegaal W, Koekman A, van Dooremalen S, Pasterkamp G, de Groot PG, Cicardi M, Renné T, Maas C.
    J Allergy Clin Immunol; 2016 Nov 01; 138(5):1414-1423.e9. PubMed ID: 27130860
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  • 4. Hereditary angioedema with normal C1-inhibitor: Clinical and genetic characterization of 15 Portuguese unrelated families.
    Dias de Castro E, Pinhal AL, Bragança M, Parente Freixo J, Martinho A.
    Ann Allergy Asthma Immunol; 2024 Jun 01; 132(6):730-736. PubMed ID: 38342132
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  • 5. 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 01; 185(3):332-7. PubMed ID: 27271546
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  • 7. Diagnosis and treatment of bradykinin-mediated angioedema: outcomes from an angioedema expert consensus meeting.
    Craig TJ, Bernstein JA, Farkas H, Bouillet L, Boccon-Gibod I.
    Int Arch Allergy Immunol; 2014 Sep 01; 165(2):119-27. PubMed ID: 25401373
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  • 9. Pathogenic mechanisms of bradykinin mediated diseases: dysregulation of an innate inflammatory pathway.
    Kaplan AP, Joseph K.
    Adv Immunol; 2014 Sep 01; 121():41-89. PubMed ID: 24388213
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  • 11. 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 01; 137(6):1822-1829.e1. PubMed ID: 26395818
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  • 15. Recent advances in the management of hereditary angioedema.
    Hemperly SE, Agarwal NS, Xu YY, Zhi YX, Craig TJ.
    J Am Osteopath Assoc; 2013 Jul 01; 113(7):546-55. PubMed ID: 23843378
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  • 19. Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel SERPING1 mutations and genetic factors modifying the clinical phenotype.
    Grivčeva-Panovska V, Košnik M, Korošec P, Andrejević S, Karadža-Lapić L, Rijavec M.
    Ann Med; 2018 May 01; 50(3):269-276. PubMed ID: 29513108
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