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Pubmed for Handhelds

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Journal Abstract Search

210 related items for PubMed ID: 31397881

  • 21. Acquired angioedema--occurrence, clinical features and associated disorders in a Danish nationwide patient cohort.
    Bygum A, Vestergaard H.
    Int Arch Allergy Immunol; 2013; 162(2):149-55. PubMed ID: 23921495
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  • 24. Restriction of C1-inhibitor activity in hereditary angioedema by dominant-negative effects of disease-associated SERPING1 gene variants.
    Ryø LB, Haslund D, Rovsing AB, Pihl R, Sanrattana W, de Maat S, Palarasah Y, Maas C, Thiel S, Mikkelsen JG.
    J Allergy Clin Immunol; 2023 Nov; 152(5):1218-1236.e9. PubMed ID: 37301409
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  • 26. C1-inhibitor (C1-INH) autoantibodies in hereditary angioedema. Strong correlation with the severity of disease in C1-INH concentrate naïve patients.
    Varga L, Széplaki G, Visy B, Füst G, Harmat G, Miklós K, Németh J, Cervenak L, Karádi I, Farkas H.
    Mol Immunol; 2007 Feb; 44(6):1454-60. PubMed ID: 16750855
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  • 27. Hereditary angioedema with normal C1 inhibitor function: consensus of an international expert panel.
    Zuraw BL, Bork K, Binkley KE, Banerji A, Christiansen SC, Castaldo A, Kaplan A, Riedl M, Kirkpatrick C, Magerl M, Drouet C, Cicardi M.
    Allergy Asthma Proc; 2012 Feb; 33 Suppl 1():S145-56. PubMed ID: 23394603
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  • 29. Successful Use of Recombinant Human C1-INH in a Patient with Acquired Angioedema due to C1 Inhibitor Deficiency and an Unusually High Titer of Anti-C1-Inhibitor Autoantibodies.
    Jesenak M, Brndiarova M, Banovcin P, Varga L, Farkas H.
    J Investig Allergol Clin Immunol; 2021 Jun 22; 31(3):255-256. PubMed ID: 32732186
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  • 31. Acquired C1 Inhibitor Deficiency.
    Otani IM, Banerji A.
    Immunol Allergy Clin North Am; 2017 Aug 22; 37(3):497-511. PubMed ID: 28687105
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  • 33. Angioedema with acquired deficiency of the C1 inhibitor: a constellation of syndromes.
    Frigas E.
    Mayo Clin Proc; 1989 Oct 22; 64(10):1269-75. PubMed ID: 2687589
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  • 34. SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes.
    Ponard D, Gaboriaud C, Charignon D, Ghannam A, Wagenaar-Bos IGA, Roem D, López-Lera A, López-Trascasa M, Tosi M, Drouet C.
    Hum Mutat; 2020 Jan 22; 41(1):38-57. PubMed ID: 31517426
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  • 36. A nationwide study of acquired C1-inhibitor deficiency in France: Characteristics and treatment responses in 92 patients.
    Gobert D, Paule R, Ponard D, Levy P, Frémeaux-Bacchi V, Bouillet L, Boccon-Gibod I, Drouet C, Gayet S, Launay D, Martin L, Mekinian A, Leblond V, Fain O.
    Medicine (Baltimore); 2016 Aug 22; 95(33):e4363. PubMed ID: 27537564
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  • 38. Genetic test indications and interpretations in patients with hereditary angioedema.
    Weiler CR, van Dellen RG.
    Mayo Clin Proc; 2006 Jul 22; 81(7):958-72. PubMed ID: 16835976
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  • 39. Angioedema due to acquired C1-inhibitor deficiency: a bridging condition between autoimmunity and lymphoproliferation.
    Cugno M, Castelli R, Cicardi M.
    Autoimmun Rev; 2008 Dec 22; 8(2):156-9. PubMed ID: 19014872
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  • 40. Shortened Activated Partial Thromboplastin Time May Help in Diagnosing Hereditary and Acquired Angioedema.
    Bork K, Witzke G.
    Int Arch Allergy Immunol; 2016 Dec 22; 170(2):101-7. PubMed ID: 27463190
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