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Journal Abstract Search

354 related items for PubMed ID: 1489854

  • 1. The C1 inhibitor deficiency. A review.
    Carreer FM.
    Eur J Clin Chem Clin Biochem; 1992 Dec; 30(12):793-807. PubMed ID: 1489854
    [Abstract] [Full Text] [Related]

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

  • 3. [C1 inhibitor deficiency. Heredity and acquired forms. Symptoms, diagnostic and therapeutic problems].
    Obtułowicz K, Kapusta M, Obtułowicz A, Mazurkiewicz A.
    Przegl Lek; 2002 Dec; 59(6):438-41. PubMed ID: 12418282
    [Abstract] [Full Text] [Related]

  • 4. Autoantibody-mediated acquired deficiency of C1 inhibitor.
    Alsenz J, Bork K, Loos M.
    N Engl J Med; 1987 May 28; 316(22):1360-6. PubMed ID: 3494945
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Autoantibody facilitated cleavage of C1-inhibitor in autoimmune angioedema.
    Jackson J, Sim RB, Whaley K, Feighery C.
    J Clin Invest; 1989 Feb 30; 83(2):698-707. PubMed ID: 2536404
    [Abstract] [Full Text] [Related]

  • 7. The acquired C1-INH deficiencies with autoantibodies (AAE type II).
    Alsenz J, Loos M.
    Behring Inst Mitt; 1989 Jul 30; (84):165-72. PubMed ID: 2679532
    [Abstract] [Full Text] [Related]

  • 8. 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 30; 44(8):1836-40. PubMed ID: 11508436
    [Abstract] [Full Text] [Related]

  • 9. Symptoms, course, and complications of abdominal attacks in hereditary angioedema due to C1 inhibitor deficiency.
    Bork K, Staubach P, Eckardt AJ, Hardt J.
    Am J Gastroenterol; 2006 Mar 30; 101(3):619-27. PubMed ID: 16464219
    [Abstract] [Full Text] [Related]

  • 10. [Angioedema due to acquired complement-C1-inhibitor deficiency in a female patient with non-Hodgkin lymphoma and autoimmune hemolytic anemia].
    Beretta KR, Späth PJ, Pedrazzini A, Martinelli G, Cavalli F.
    Schweiz Med Wochenschr; 1991 Jun 22; 121(25):943-7. PubMed ID: 1862309
    [Abstract] [Full Text] [Related]

  • 11. Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course.
    Bork K, Gül D, Hardt J, Dewald G.
    Am J Med; 2007 Nov 22; 120(11):987-92. PubMed ID: 17976427
    [Abstract] [Full Text] [Related]

  • 12. Clinical, biochemical, and genetic characterization of a novel estrogen-dependent inherited form of angioedema.
    Binkley KE, Davis A.
    J Allergy Clin Immunol; 2000 Sep 22; 106(3):546-50. PubMed ID: 10984376
    [Abstract] [Full Text] [Related]

  • 13. Response of variant hereditary angioedema phenotypes to danazol therapy. Genetic implications.
    Gadek JE, Hosea SW, Gelfand JA, Frank MM.
    J Clin Invest; 1979 Jul 22; 64(1):280-6. PubMed ID: 376558
    [Abstract] [Full Text] [Related]

  • 14. [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]

  • 15. [Hereditary angioedema. A hereditary disorder in the synthesis of the complement system].
    Vanderstock L, Vander Eecken P, Vermeersch H.
    Acta Otorhinolaryngol Belg; 1983 Feb 20; 36(3):418-31. PubMed ID: 6613563
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Hereditary angioedema: diagnosis and management.
    Chng HH, Boey ML.
    Singapore Med J; 1990 Apr 20; 31(2):177-9. PubMed ID: 2371584
    [Abstract] [Full Text] [Related]

  • 18. [Deficiencies of C1 inhibitor: hereditary and acquired angioedema].
    Porcel-Pérez JM, López-Trascasa M.
    Rev Clin Esp; 1996 Mar 20; 196 Spec No():26-30. PubMed ID: 9206804
    [No Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Acquired C1-inhibitor deficiency.
    Frank M.
    Behring Inst Mitt; 1989 Jul 20; (84):161-4. PubMed ID: 2679531
    [No Abstract] [Full Text] [Related]

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