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PUBMED FOR HANDHELDS

Journal Abstract Search


364 related items for PubMed ID: 18758157

  • 41.
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  • 42. The future of therapeutic options for hereditary angioedema.
    Smith TD, Riedl MA.
    Ann Allergy Asthma Immunol; 2024 Oct; 133(4):380-390. PubMed ID: 38679158
    [Abstract] [Full Text] [Related]

  • 43. Evidence for a dominant-negative effect of a missense mutation in the SERPING1 gene responsible for hereditary angioedema type I.
    Yasuno S, Ansai O, Hayashi R, Nakamura S, Shimomura Y.
    J Dermatol; 2021 Aug; 48(8):1243-1249. PubMed ID: 33914953
    [Abstract] [Full Text] [Related]

  • 44. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 45. Genetics of Hereditary Angioedema Revisited.
    Germenis AE, Speletas M.
    Clin Rev Allergy Immunol; 2016 Oct; 51(2):170-82. PubMed ID: 27116602
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  • 51. First case of homozygous C1 inhibitor deficiency.
    Blanch A, Roche O, Urrutia I, Gamboa P, Fontán G, López-Trascasa M.
    J Allergy Clin Immunol; 2006 Dec; 118(6):1330-5. PubMed ID: 17137866
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  • 53. Hereditary angioedema: management of laryngeal attacks.
    Christiansen SC, Zuraw BL.
    Am J Rhinol Allergy; 2011 Dec; 25(6):379-82. PubMed ID: 22185739
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  • 58. Safety and efficacy of prophylactic nanofiltered C1-inhibitor in hereditary angioedema.
    Zuraw BL, Kalfus I.
    Am J Med; 2012 Sep; 125(9):938.e1-7. PubMed ID: 22800873
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  • 60. [Hereditary angioedema--pathophysiology, genetics, symptoms].
    Muszyńska A, Janocha E, Fal AM.
    Pol Merkur Lekarski; 2008 Jul; 25(145):90-3. PubMed ID: 18839624
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