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Journal Abstract Search

219 related items for PubMed ID: 8438855

  • 1. Angioedema presenting as chronic gastrointestinal symptoms.
    Eck SL, Morse JH, Janssen DA, Emerson SG, Markovitz DM.
    Am J Gastroenterol; 1993 Mar; 88(3):436-9. PubMed ID: 8438855
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  • 3. 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; 101(3):619-27. PubMed ID: 16464219
    [Abstract] [Full Text] [Related]

  • 4. [Hereditary angioedema. A rare cause of acute abdominal pain with ascites].
    Goti F, Melcher GA, Späth P, Wüthrich B.
    Dtsch Med Wochenschr; 1998 Oct 02; 123(40):1166-71. PubMed ID: 9793531
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  • 5. [Recurrent attacks of angioedema ascribed to the use of estrogen preparations and a pregnancy (hereditary angioedema type 3)].
    van der Klooster JM, Schelfhout LJ, Grootendorst AF, Zweers PG.
    Ned Tijdschr Geneeskd; 2002 Aug 24; 146(34):1599-602. PubMed ID: 12224485
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  • 6. [Hereditary angioedema C1 inhibitor deficiency].
    Fain O.
    Rev Prat; 2007 Mar 31; 57(6):591. PubMed ID: 17593781
    [No Abstract] [Full Text] [Related]

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  • 8. Hereditary angioedema: an infrequent cause of abdominal pain with ascites.
    Talavera A, Larraona JL, Ramos JL, López T, Maraver A, Arias J, Barrios A.
    Am J Gastroenterol; 1995 Mar 31; 90(3):471-4. PubMed ID: 7872288
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  • 10. Treatment with C1 inhibitor concentrate in abdominal pain attacks of patients with hereditary angioedema.
    Bork K, Meng G, Staubach P, Hardt J.
    Transfusion; 2005 Nov 31; 45(11):1774-84. PubMed ID: 16271103
    [Abstract] [Full Text] [Related]

  • 11. Recurrent abdominal pain due to hereditary angio-oedema.
    Landau Z, Even-Tov S, Barsily N, Resnitzky P.
    Eur J Med; 1993 May 31; 2(5):305-6. PubMed ID: 8252164
    [No Abstract] [Full Text] [Related]

  • 12. [Hereditary deficiency of C1-esterase inhibitor presenting with recurrent abdominal pain].
    Steiss JO, Mayser P, Gortner L, Alzen G.
    Klin Padiatr; 2002 May 31; 214(1):20-1. PubMed ID: 11823949
    [Abstract] [Full Text] [Related]

  • 13. 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
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  • 14. Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course.
    Bork K, Gül D, Hardt J, Dewald G.
    Am J Med; 2007 Nov 28; 120(11):987-92. PubMed ID: 17976427
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  • 15. Glomerulonephritis and hereditary angioedema: report of 2 cases.
    Hory B, Haultier JJ.
    Clin Nephrol; 1989 May 28; 31(5):259-63. PubMed ID: 2736814
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  • 16. [C1 inhibitor deficiency. Heredity and acquired forms. Symptoms, diagnostic and therapeutic problems].
    Obtułowicz K, Kapusta M, Obtułowicz A, Mazurkiewicz A.
    Przegl Lek; 2002 May 28; 59(6):438-41. PubMed ID: 12418282
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  • 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 28; 44(8):1836-40. PubMed ID: 11508436
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  • 19. [Simultaneous occurrence of hereditary angioneurotic edema and Crohn disease].
    Farkas H, Gyeney L, Nemesánszky E, Káldi G, Kukán F, Masszi I, Soós J, Bély M, Farkas E, Füst G, Varga L.
    Orv Hetil; 1998 May 10; 139(19):1165-9. PubMed ID: 9613166
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  • 20. C1 inhibitor deficiency: diagnosis.
    Gompels MM, Lock RJ.
    Clin Exp Dermatol; 2005 Jul 10; 30(4):460-2. PubMed ID: 15953110
    [Abstract] [Full Text] [Related]

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