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Journal Abstract Search

898 related items for PubMed ID: 18655790

  • 1. Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations.
    Wagenaar-Bos IG, Drouet C, Aygören-Pursun E, Bork K, Bucher C, Bygum A, Farkas H, Fust G, Gregorek H, Hack CE, Hickey A, Joller-Jemelka HI, Kapusta M, Kreuz W, Longhurst H, Lopez-Trascasa M, Madalinski K, Naskalski J, Nieuwenhuys E, Ponard D, Truedsson L, Varga L, Nielsen EW, Wagner E, Zingale L, Cicardi M, van Ham SM.
    J Immunol Methods; 2008 Sep 30; 338(1-2):14-20. PubMed ID: 18655790
    [Abstract] [Full Text] [Related]

  • 2. [Hereditary or acquired angioedema caused by functional deficiency of C1 inhibitor--a still unfamiliar disease picture].
    Wüthrich B, Devay J, Späth P.
    Schweiz Med Wochenschr; 1999 Feb 20; 129(7):285-91. PubMed ID: 10093876
    [Abstract] [Full Text] [Related]

  • 3. Paternal mosaicism and hereditary angioedema in a Taiwanese family.
    Yu TC, Shyur SD, Huang LH, Wen DC, Li JS.
    Ann Allergy Asthma Immunol; 2007 Oct 20; 99(4):375-9. PubMed ID: 17941288
    [Abstract] [Full Text] [Related]

  • 4. 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 20; 44(6):1454-60. PubMed ID: 16750855
    [Abstract] [Full Text] [Related]

  • 5. Hereditary angioedema: a decade of human C1-inhibitor concentrate therapy.
    Farkas H, Jakab L, Temesszentandrási G, Visy B, Harmat G, Füst G, Széplaki G, Fekete B, Karádi I, Varga L.
    J Allergy Clin Immunol; 2007 Oct 20; 120(4):941-7. PubMed ID: 17761272
    [Abstract] [Full Text] [Related]

  • 6. Hereditary angioedema: therapeutic effect of danazol on C4 and C1 esterase inhibitors.
    Fabiani JE, Paulin P, Simkin G, Leoni J, Palombarani S, Squiquera L.
    Ann Allergy; 1990 Apr 20; 64(4):388-92. PubMed ID: 2108593
    [Abstract] [Full Text] [Related]

  • 7. Is there a need for clinical guidelines in the United States for the diagnosis of hereditary angioedema and the screening of family members of affected patients?
    Lunn ML, Santos CB, Craig TJ.
    Ann Allergy Asthma Immunol; 2010 Mar 20; 104(3):211-4. PubMed ID: 20377110
    [Abstract] [Full Text] [Related]

  • 8. [Hereditary angioedema, a rare cause of recurrent abdominal pains. A report of 2 clinical cases and comments of a general nature].
    Parisi G, Chiarelli A, Squadrone NP, Galante E.
    Minerva Pediatr; 1991 May 20; 43(5):413-7. PubMed ID: 1842037
    [Abstract] [Full Text] [Related]

  • 9. Diagnosis and management of hereditary angioedema (HAE).
    Atkinson JP.
    Ann Allergy; 1979 Jun 20; 42(6):348-52. PubMed ID: 378041
    [Abstract] [Full Text] [Related]

  • 10. A first of its kind quantitative functional C1-esterase inhibitor lateral flow assay for hereditary angioedema point-of-care diagnostic testing.
    Chockalingam PS, Zhou Z, Garg BK, Boehringer H, Chung R, Fait S.
    Int Immunopharmacol; 2020 Jun 20; 83():106526. PubMed ID: 32361670
    [Abstract] [Full Text] [Related]

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  • 13. Unmasking of acquired autoimmune C1-inhibitor deficiency by an angiotensin-converting enzyme inhibitor.
    Kleiner GI, Giclas P, Stadtmauer G, Cunningham-Rundles C.
    Ann Allergy Asthma Immunol; 2001 Apr 20; 86(4):461-4. PubMed ID: 11345293
    [Abstract] [Full Text] [Related]

  • 14. A new type of acquired C1 inhibitor deficiency associated with systemic lupus erythematosus.
    Cacoub P, Frémeaux-Bacchi V, De Lacroix I, Guillien F, Kahn MF, Kazatchkine MD, Godeau P, Piette JC.
    Arthritis Rheum; 2001 Aug 20; 44(8):1836-40. PubMed ID: 11508436
    [Abstract] [Full Text] [Related]

  • 15. Genetic test indications and interpretations in patients with hereditary angioedema.
    Weiler CR, van Dellen RG.
    Mayo Clin Proc; 2006 Jul 20; 81(7):958-72. PubMed ID: 16835976
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  • 17. Autoantibodies and lymphoproliferative diseases in acquired C1-inhibitor deficiencies.
    Cicardi M, Zingale LC, Pappalardo E, Folcioni A, Agostoni A.
    Medicine (Baltimore); 2003 Jul 20; 82(4):274-81. PubMed ID: 12861105
    [Abstract] [Full Text] [Related]

  • 18. Hereditary and acquired deficiencies of C1 inhibitor.
    Davis AE.
    Immunodefic Rev; 1989 Jul 20; 1(3):207-26. PubMed ID: 2698641
    [Abstract] [Full Text] [Related]

  • 19. C1 inhibitor and diagnosis of hereditary angioedema in newborns.
    Nielsen EW, Johansen HT, Holt J, Mollnes TE.
    Pediatr Res; 1994 Feb 20; 35(2):184-7. PubMed ID: 8165053
    [Abstract] [Full Text] [Related]

  • 20. Factor VIIa in patients with C1-inhibitor deficiency.
    Nielsen EW, Morrissey J, Olsen JO, Osterud B.
    Thromb Haemost; 1995 Oct 20; 74(4):1103-6. PubMed ID: 8560420
    [Abstract] [Full Text] [Related]

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