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377 related items for PubMed ID: 2698641

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

  • 2. C1-inhibitor--biochemical properties and clinical applications.
    Al-Abdullah IH, Greally J.
    Crit Rev Immunol; 1985; 5(4):317-30. PubMed ID: 3899511
    [Abstract] [Full Text] [Related]

  • 3. Structure and function of C1 inhibitor.
    Davis AE.
    Behring Inst Mitt; 1989 Jul; (84):142-50. PubMed ID: 2679529
    [Abstract] [Full Text] [Related]

  • 4. Plasma levels of C1- inhibitor complexes and cleaved C1- inhibitor in patients with hereditary angioneurotic edema.
    Cugno M, Nuijens J, Hack E, Eerenberg A, Frangi D, Agostoni A, Cicardi M.
    J Clin Invest; 1990 Apr; 85(4):1215-20. PubMed ID: 2318974
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. [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]

  • 7. [Hereditary angioneurotic edema: a molecular disease caused by a defect in the O-glycosylation of C1 esterase inhibitor (C1-INH)].
    Ollier-Hartmann MP, Strecker G, Montreuil J, Hartmann L.
    C R Acad Sci III; 1984 Feb 20; 299(16):667-9. PubMed ID: 6440668
    [Abstract] [Full Text] [Related]

  • 8. The acquired C1-INH deficiencies with autoantibodies (AAE type II).
    Alsenz J, Loos M.
    Behring Inst Mitt; 1989 Jul 20; (84):165-72. PubMed ID: 2679532
    [Abstract] [Full Text] [Related]

  • 9. Angioedema due to acquired C1-esterase inhibitor deficiency in a patient with Helicobacter pylori infection.
    Farkas H, Gyeney L, Majthényi P, Füst G, Varga L.
    Z Gastroenterol; 1999 Jun 20; 37(6):513-8. PubMed ID: 10427658
    [Abstract] [Full Text] [Related]

  • 10. Variability in purified dysfunctional C1(-)-inhibitor proteins from patients with hereditary angioneurotic edema. Functional and analytical gel studies.
    Donaldson VH, Harrison RA, Rosen FS, Bing DH, Kindness G, Canar J, Wagner CJ, Awad S.
    J Clin Invest; 1985 Jan 20; 75(1):124-32. PubMed ID: 3965500
    [Abstract] [Full Text] [Related]

  • 11. Unique C1 inhibitor dysfunction in a kindred without angioedema. I. A mutant C1 INH that inhibits C1-s but not C1-r.
    Wisnieski JJ, Knauss TC, Yike I, Dearborn DG, Narvy RL, Naff GB.
    J Immunol; 1994 Mar 15; 152(6):3199-209. PubMed ID: 8144914
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 99(4):375-9. PubMed ID: 17941288
    [Abstract] [Full Text] [Related]

  • 13. Autoantibodies and lymphoproliferative diseases in acquired C1-inhibitor deficiencies.
    Cicardi M, Zingale LC, Pappalardo E, Folcioni A, Agostoni A.
    Medicine (Baltimore); 2003 Jul 15; 82(4):274-81. PubMed ID: 12861105
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Mutations in the C1 inhibitor gene that result in hereditary angioneurotic edema.
    Davis AE, Bissler JJ, Cicardi M.
    Behring Inst Mitt; 1993 Dec 30; (93):313-20. PubMed ID: 8172583
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. 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]

  • 18. Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema.
    Cicardi M, Igarashi T, Rosen FS, Davis AE.
    J Clin Invest; 1987 Mar 30; 79(3):698-702. PubMed ID: 3818946
    [Abstract] [Full Text] [Related]

  • 19. [C1 inhibitor deficiency. Heredity and acquired forms. Symptoms, diagnostic and therapeutic problems].
    Obtułowicz K, Kapusta M, Obtułowicz A, Mazurkiewicz A.
    Przegl Lek; 2002 Mar 30; 59(6):438-41. PubMed ID: 12418282
    [Abstract] [Full Text] [Related]

  • 20. Polyclonal autoantibodies against C1 inhibitor in a case of acquired angioedema.
    Ponce IM, Caballero T, Reche M, Piteiro AB, López-Serrano MC, Fontán G, López-Trascasa M.
    Ann Allergy Asthma Immunol; 2002 Jun 30; 88(6):632-7. PubMed ID: 12086372
    [Abstract] [Full Text] [Related]

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