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Journal Abstract Search

280 related items for PubMed ID: 7172497

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

  • 22. 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; 44(6):1454-60. PubMed ID: 16750855
    [Abstract] [Full Text] [Related]

  • 23. Hageman factor-dependent pathways: mechanism of initiation and bradykinin formation.
    Kaplan AP.
    Fed Proc; 1983 Nov; 42(14):3123-7. PubMed ID: 6556144
    [Abstract] [Full Text] [Related]

  • 24. 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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  • 25.
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  • 26. Inhibition of vascular permeability by antisense-mediated inhibition of plasma kallikrein and coagulation factor 12.
    Bhattacharjee G, Revenko AS, Crosby JR, May C, Gao D, Zhao C, Monia BP, MacLeod AR.
    Nucleic Acid Ther; 2013 Jun; 23(3):175-87. PubMed ID: 23582057
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  • 29. Rapid fibrinolysis, augmented Hageman factor (factor XII) titers, and decreased C1 esterase inhibitor titers in women taking oral contraceptives.
    Gordon EM, Ratnoff OD, Saito H, Donaldson VH, Pensky J, Jones PK.
    J Lab Clin Med; 1980 Nov; 96(5):762-9. PubMed ID: 7419960
    [Abstract] [Full Text] [Related]

  • 30. Hereditary angioedema: case report of a family.
    Yilmaz M, Kendirli SG, Altintaş D, Bingöl G.
    Turk J Pediatr; 2000 Nov; 42(3):230-3. PubMed ID: 11105624
    [Abstract] [Full Text] [Related]

  • 31. Treatment of episodes of hereditary angioedema with C1 inhibitor: serial assessment of observed abnormalities of the plasma bradykinin-forming pathway and fibrinolysis.
    Joseph K, Tholanikunnel TE, Kaplan AP.
    Ann Allergy Asthma Immunol; 2010 Jan; 104(1):50-4. PubMed ID: 20143645
    [Abstract] [Full Text] [Related]

  • 32. [Hereditary angioedema: clinical and laboratory aspects of 7 cases].
    Moschione-Castro AP, Croce J, Diogo CL, Jacob CM, Pastorino AC, Kirschfink M, Grumach AS.
    Rev Hosp Clin Fac Med Sao Paulo; 1998 Jan; 53(1):21-5. PubMed ID: 9659739
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  • 34. [Immunologic parameters in chronic urticaria].
    Malet A, Engel P, Huguet J, García-Calderón PA.
    Allergol Immunopathol (Madr); 1986 Jan; 14(5):375-81. PubMed ID: 3799406
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  • 35. Factor VIIa in patients with C1-inhibitor deficiency.
    Nielsen EW, Morrissey J, Olsen JO, Osterud B.
    Thromb Haemost; 1995 Oct; 74(4):1103-6. PubMed ID: 8560420
    [Abstract] [Full Text] [Related]

  • 36. The bradykinin-forming cascade and its role in hereditary angioedema.
    Kaplan AP, Joseph K.
    Ann Allergy Asthma Immunol; 2010 Mar; 104(3):193-204. PubMed ID: 20377108
    [Abstract] [Full Text] [Related]

  • 37. Inherited C1 inhibitor deficiency.
    Agostoni A.
    Complement Inflamm; 1989 Mar; 6(2):112-8. PubMed ID: 2656079
    [Abstract] [Full Text] [Related]

  • 38. [A study of coagulation contact factors in hereditary angioneurotic oedema (author's transl)].
    Soulier JP, Gozin D, Ollier-Hartmann MP, Hartmann L.
    Nouv Presse Med; 1981 May 02; 10(20):1627-31. PubMed ID: 6166918
    [Abstract] [Full Text] [Related]

  • 39. [Pathogenesis of hereditary angioedema].
    Reimold WV.
    Z Gastroenterol; 1987 Jun 02; 25(6):316-24. PubMed ID: 3617844
    [Abstract] [Full Text] [Related]

  • 40. Chronic urticaria.
    Zauli D, Deleonardi G, Grassi A, Bortolotti R, Lari F, Ballardini G, Bianchi FB.
    Arch Dermatol; 2001 Apr 02; 137(4):504-5. PubMed ID: 11295939
    [No Abstract] [Full Text] [Related]

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