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Journal Abstract Search

364 related items for PubMed ID: 18758157

  • 21. Detection of C1 inhibitor mutations in patients with hereditary angioedema.
    Zuraw BL, Herschbach J.
    J Allergy Clin Immunol; 2000 Mar; 105(3):541-6. PubMed ID: 10719305
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  • 23. [Identification of a novel mutation of C1 inhibitor gene in a Chinese family with hereditary angioedema].
    Zhi YX, Zhang HY, Huang SZ.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Dec; 25(6):664-6. PubMed ID: 14714307
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  • 24. The pathogenesis of hereditary angioedema.
    Davis AE.
    Transfus Apher Sci; 2003 Dec; 29(3):195-203. PubMed ID: 14572810
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  • 27. Specific Targeting of Plasma Kallikrein for Treatment of Hereditary Angioedema: A Revolutionary Decade.
    Busse P, Kaplan A.
    J Allergy Clin Immunol Pract; 2022 Mar; 10(3):716-722. PubMed ID: 34838707
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  • 28. Mutational spectrum of the SERPING1 gene in Swiss patients with hereditary angioedema.
    Steiner UC, Keller M, Schmid P, Cichon S, Wuillemin WA.
    Clin Exp Immunol; 2017 Jun; 188(3):430-436. PubMed ID: 28194776
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  • 30. Enzymatic pathways in the pathogenesis of hereditary angioedema: the role of C1 inhibitor therapy.
    Kaplan AP.
    J Allergy Clin Immunol; 2010 Nov; 126(5):918-25. PubMed ID: 20889195
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  • 31. Five novel mutations in the C1 inhibitor gene (C1NH) leading to a premature stop codon in patients with type I hereditary angioedema.
    Freiberger T, Kolárová L, Mejstrík P, Vyskocilová M, Kuklínek P, Litzman J.
    Hum Mutat; 2002 Apr; 19(4):461. PubMed ID: 11933207
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  • 32. Clinical, biochemical, and genetic characterization of a novel estrogen-dependent inherited form of angioedema.
    Binkley KE, Davis A.
    J Allergy Clin Immunol; 2000 Sep; 106(3):546-50. PubMed ID: 10984376
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  • 35. [Hereditary angioedema: new mechanisms and therapeutic options].
    Reshef A, Leibovich I, Goren A, Kidon M.
    Harefuah; 2009 Aug; 148(8):529-34, 571. PubMed ID: 19899257
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  • 37. Hereditary C1 inhibitor deficiency is associated with high spontaneous amidase activity.
    Charignon D, Ghannam A, Ponard D, Drouet C.
    Mol Immunol; 2017 May; 85():120-122. PubMed ID: 28222330
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  • 38. The Turkish Hereditary Angioedema Pilot Study (TURHAPS): the first Turkish series of hereditary angioedema.
    Kesim B, Uyguner ZO, Gelincik A, Mete Gökmen N, Sin AZ, Karakaya G, Erdenen F, Ardeniz O, Ozşeker F, Gülbahar O, Colakoğlu B, Dal M, Büyüköztürk S.
    Int Arch Allergy Immunol; 2011 May; 156(4):443-50. PubMed ID: 21832835
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  • 40. sgp120 and the contact system in hereditary angioedema: A diagnostic tool in HAE with normal C1 inhibitor.
    Larrauri B, Hester CG, Jiang H, Miletic VD, Malbran A, Bork K, Kaplan A, Frank M.
    Mol Immunol; 2020 Mar; 119():27-34. PubMed ID: 31955064
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