Referanser

1. Quincke H. Über akutes umschriebenes Hautödem. Monatsschr Prakt Dermat 1882; 1: 129

2. Hawthorne N. The House of the Seven Gables. New York: Bantam; 1851. 1p.

3. Dennehy JJ. Hereditary angioneurotic edema: report of a large kindred with defect in C-prime-1 esterase inhibitor and review of the literature. Ann Intern Med 1970; 73: 55-9.

4. Donaldson VH, Rosen FS. Hereditary angioneurotic edema: A clinical survey. Pediatrics 1966; 37: 1017-27.

5. Blohme G, Ysander K, Korsan-Bengtsen K, Laurell AB. Hereditary angioneurotic oedema in three families. Acta med scand 1972; 19: 209-19.

6. Ohela K. Hereditary angioneurotic oedema in Finland. Clinical. Acta med scand 1977; 201: 415-27.

7. Streuli R, Grob P. Untersuchung einer grossen Sippe mit hereditärem angioneurotischem Ödem. Scweiz med Wschr 1975; 43: 1382-7.

8. Bork K. Hereditary angioedema (HAE) due to C1 esterase inhibitor deficiency. Biomed Progr 1990; 1: 9-13.

9. Moore GP, Hurley WT, Pace SA. Hereditary angioedema. Ann Emerg Med 1988; 17: 1082-6.

10. Davis AE. C1 Inhibitor and hereditary angioneurotic edema. Ann Rev Immunol 1988; 6: 595-628.

11. Agostoni A, Cicardi M. Hereditary and acquired C1-inhibitor deficiency: biological and clinical characteristics in 235 patients. Medicine Baltimore 1992; 71: 206-15.

12. Cicardi M, Bergamaschini L, Cugno M, Beretta A, Zingale LC, Colombo M, Agostoni A. Pathogenetic and clinical aspects of C1 inhibitor deficiency. Immunobiology 1998; 199(2): 366-76.

13. Warin RP. The role of trauma in the spreading weals of hereditary angio- oedema. Br J Dermatol 1983; 108: 189-94.

14. Lundh B, Laurell AB , Wetterqvist H, White T, Granerus G. A case of hereditary angioneurotic oedema, successfully treated with epsilon-aminocaproic acid. Studies on C'1 esterase inhibitor, C'1 activation, plasminogen level and histamine metabolism. Clin Exp Immunol 1968; 3: 733-45.

15. Arnoldsson H, Belin L, Hallberg L, Helander E, Lindholm B, Westling H. Hereditary periodic oedema. Acta med scand 1967; 181: 115

16. Cohen N, Sharon A, Golik A, Zaidenstein R, Modai D. Hereditary angioneurotic edema with severe hypovolemic shock. J Clin Gastroenterol 1993; 16: 237-9.

17. Kennedy PS, Goyal RK, Hersh T. Hereditary angioneurotic edema. A case with recurring abdominal pain. Am J Dig Dis 1972; 17: 435-8.

18. Zuraw BL. C1-Inhibitor Deficiency and Autoimmunity. Immunol Allergy Clin N Amer 1993; 13: 441-57.

19. Marenah CB, Quiney JR. C1 esterase inhibitor deficiency as a cause of abdominal pain. BMJ 1983; 286: 786-7.

20. Weinstock LB, Kothari T, Sharma RN, Rosenfeld SI. Recurrent abdominal pain as the sole manifestation of hereditary angioedema in multiple family members. Gastroenterology 1987; 93: 1116-8.

21. Shah TJ, Knowles WO , Mcgeady SJ. Hereditary angioedema with recurrent abdominal pain and ascites. J Allerg Clin Immunol 1995; 96: 259-61.

22. Shinzato T, Nakamura H, Kuniyoshi T, Higashionna A, Uehara T, Oshiro J, Uechi H, Shikiya K, Sakugawa H, Kinjo F, et-al. Hereditary angioedema: a case with ascites yet no symptoms in the family. Intern Med 1992; 31: 633-5.

23. von-Schonfeld J, Olbricht T, Breuer N. [Hereditary angioedema type II with predominantly abdominal symptoms]. Dtsch Med Wochenschr 1991; 116: 973-6.

24. Burghardt W, Wernze H. Ultrasonography for early diagnosis of hereditary angioneurotic oedema. Lancet 1987; 2(8551): 165-.

25. Laurent J, Toulet R , Lagrue G, Cicardi M, Bergamaschini L, Marasini B, Boccasini G, Tucci A, Agostoni A. Ultrasonography in the diagnosis of hereditary angioneurotic oedema (Letter). Lancet 1988; ii: 761-.

26. Reimold WV. Hereditäres Angioödem (HAE) mit akuter gastrointestinaler Symptomatik. Eine seltene Differentialdiagnose bei akutem Abdomen. Med Klin 1987; 82: 900-7.

27. Collen MJ, Lewis JH , Deschner WK, Ansher AF, Zurlo JJ, Benjamin SB, Frank MM. Abdominal pain in hereditary angioedema: the role of acid hypersecretion. Am J Gastroenterol 1989; 84: 873-7.

28. Granerus G, Hallberg L, Laurell AB, Wetterquist H. Studies on the histamine metabolism and the complement system in hereditary angioneurotic edema. Acta med scand 1967; 182: 11-22.

29. Lewis JH. Idiopathic gastric acid hypersecretion: treatment implications for refractory acid/peptic disorders. Aliment Pharmacol Ther 1991; 5 Suppl 1: 15-24.

30. Zeana C. Hereditary angioedema due to deficit of C1-esterase inhibitor. Rev Roum Med -Med Int 1989; 27(2): 143-7.

31. Diaz-Isaacs M. [Hereditary angioedema. Review and presentation of 2 cases in a family]. Rev Med Panama 1991; 16: 143-50.

32. Nielsen EW, Kjernlie DF, Aaseth J. Dødsfall av hereditært angioødem (A fatal outcome of hereditary angio-oedema). Tidsskr Nor Laegeforen 1995; 115(1): 43-4.

33. Wason IM. Angioneurotic Edema. Report of a case with necropsy findings. JAMA 1926; 86: 1332-3.

34. Frank MM, Gelfand JA, Atkinson JP. Hereditary angioedema: the clinical syndrome and its management. Ann Intern Med 1976; 84: 580-93.

35. Bajor K, Horgasz J, Husz S, Szilagyi I. Sudden death due to pulmonary complication in a patient with hereditary angioneuroticedema. Dermatol Monatschr 1983; 169: 468-70.

36. Coudry H, Durrleman E, Chobaut JC, Agache P, Laurent R. Glottic localizations of hereditary angioneurotic edema. [French]. JFORL J Fr Otorhinolaryngol Audiophonol Chir Maxillofac 1976; 25: 141-5.

37. Legendre M, Chiche JF, Molina C, Grouffal C, Betail G. Respiratory manifestations in hereditary angioneurotic edema. [French]. Rev Pneumol Clin 1985; 41: 251-8.

38. Juhlin L, Michaelsson G. Vascular reactions in hereditary angioneurotic edema. Acta Derm Venereol (Stockh) 1969; 49: 20-5.

39. Van Dellen RC, Myers RP. Bladder involvement in hereditary angioedema. Mayo Clin Proc 1980; 55: 277-8.

40. Starzia Z, Hegyi E, Kuklinek P, Cap J, Stefanovic J, Lokaj J. Hereditary angioedema in Czechoslovakia. Clinical, immunological, genetic and therapeutic studies in 16 families. Allerg Immunol 1988; 34: 35-42.

41. Perricone R, Pasetto N, Decarolis C, Vaquero E, Noccioli G, Panerai AE, Fontana L. Cystic Ovaries in Women Affected with Hereditary Angioedema. Clin Exp Immunol 1992; 90: 401-4.

42. Cunningham DS, Jensen JT. Hereditary angioneurotic edema in the puerperium. A case report. J Reprod Med 1991; 36: 312-3.

43. Khristova S. [A combination of chronic kidney failure with hereditary angioedema]. Vutr Boles 1990; 29: 114-7.

44. Krause KH, Rentrop U, Mehregan U. Cerebral manifestations in angioneurotic edema (author's transl). [German]. J Neurol Sci 1979; 42: 429-35.

45. Brettle RP, Dunmow RE, Milne LA, Yap PL. Angioneurotic oedema in the elderly. Scott Med J 1982; 27: 309-11.

46. Elnicki DM. Hereditary angioedema. South Med J 1992; 85 : 1084-90.

47. Hoffman U, Buss J, Voigtlaender P, Bernbeck U, Heene D. Hereditary angioedema and Aortitis. Abstract. Klin Wochenschr 1987; 65: 885-7.

48. Donaldson VH. Hereditary angioneurotic edema. Dis Mon 1979; 26: 1-37.

49. Ley SJ, Williams RC . A family with hereditary angioedema and multiple immunologic disorders. Am J Med 1987; 82: 1046-51.

50. Brickman CM, Tsokos GC, Balow JE, Lawley TJ, Santaella M, Hammer CH, Frank MM. Immunoregulatory disorders associated with hereditary angioedema. J Allergy Clin Immunol 1986; 77: 749-57.

51. Hory B, Haultier JJ . Glomerulonephritis and hereditary angioedema: Report of 2 cases. Clin Nephrol 1989; 5: 259-63.

52. Agnello V. Lupus diseases associated with hereditary and acquired deficiencies of complement. Springer Semin Immunopathol 1986; 9: 161-78.

53. Duncan IJS, Tymms KE, Carney G. Rheumatoid arthritis and hereditary angioedema. J Rheumatol 1988; 15: 700-2.

54. Youinou P, Dorval JC, Cledes J, Leroy JP, Miossec P, Masse R. A study of familial lupus erythematosus-like disease and hereditary angio-oedema treated with danazol. Br J Dermatol 1983; 108: 717-22.

55. Hory B, Blanc D. Renal manifestations of hereditary angioedema [letter]. Am J Med 1991; 90: 661-2.

56. Nomura H, Tsugawa Y , Koni I, Tofuku Y, Mabuchi H, Takeda R, Sato T. Hereditary angioedema complicated with chronic renal failure: report of sibling cases. Intern Med 1992; 31: 94-7.

57. Pan CG, Strife CF, Ward MK, Spitzer RE, McAdams AJ. Long-term follow-up of non-systemic lupus erythematosus glomerulonephritis in patients with hereditary angioedema: report of four cases. Am J Kidney Dis 1992; 19: 526-31.

58. Harrington TM, Toretti D, Pytko VF, Plotkin GR. Hereditary angioedema and coronary arteritis. Am J Med Sci 1984; 287: 50-2.

59. Vanbommel EFH, Ouwehand AJ, Mulder AH, Weimar W. Mesangiocapillary glomerulonephritis associated with hereditary angioedema. Nephron 1995; 69: 178-9.

60. Tenner AJ, Frank MM . Activator-bound C1 is less susceptible to inactivation by C1 inhibition than is fluid-phase C1. J Immunol 1986; 137: 625-30.

61. Hosoi S, Circolo A, Borsos T. Activation of human C1: analysis with Western blotting reveals slow self-activation. J immunol 1987; 139: 1602-8.

62. Laurell AB, Martensson U, Sjoholm AG. Spontaneous generation in human serum of a trimer complex containing C1 Inactivator, activated C1r and zymogen C1s. J Immunol 1987; 139: 4145-51.

63. Ziccardi RJ. The first component of human complement (C1): activation and control. [Review]. Springer Semin Immunopathol 1983; 6: 213-30.

64. Sjoholm AG. Inherited complement deficiency states: implications for immunity and immunological disease. APMIS 1990; 98: 861-74.

65. Morgan BP, Walport MJ. Complement deficiency and disease. Immunol Today 1991; 12: 301-6.

66. Whaley K, Ahmed AE. Control of immune complexes by the classical pathway. Behring Inst Mitt 1989; (84): 111-20.

67. Donaldson VH, Hess EV, McAdams AJ. Lupus-erythematosus-like disease in three unrelated women with hereditary angioneurotic edema. Ann Intern Med 1977; 86: 312-3.

68. D'Amelio R, Perricone R, De Carolis C, Pontesilli O, Matricardi PM, Fontana L. Immune complexes in hereditary angioneurotic edema (HANE). J Allergy Clin Immunol 1986; 78: 486-7.

69. Blockers M, Bork K. Kontrazeption und Schwangerschaft beim hereditaeren Angioödem. Dtsch Med Wschr 1987; 112: 507-9.

70. Farber C-M, Gourdin A, Lambermont M, Gilbert C, Van Vooren J-P. Substitution therapy for C1 esterase deficiency. Lancet 1992; 339: 119-.

71. Borradori L, Marie O, Rybojad M, Vexiau P, Morel P, Spath PJ. Hereditary angioedema and oral contraception [letter]. Dermatologica 1990; 181: 78-9.

72. Yip J, Cunliffe WJ. Hormonally exacerbated hereditary angioedema. Australas J Dermatol 1992; 33: 35-8.

73. Weidenbach H, Beckh KH, Lerch MM, Adler G. Precipitation of Hereditary Angioedema by Infectious Mononucleosis. Lancet 1993; 342: 934-5.

74. Nielsen EW, Skjeflo H. [Hereditary angioedema]. Nor Tannlaegeforen Tid 1991; 101: 10-1.

75. Scher I. Angioneurotic edema. O S,O M & O P 1963; 16: 286-90.

76. Heidemann D, Bork K . Lebensbedrohliche Larynxödeme durch geringfügige zahnärztliche Eingriffe beim hereditären angioneurotischen ödem. Dstch zahnärztl Z 1979; 34: 430-2.

77. Phillips KM, Glick M, Cohen SG. Hereditary angioedema: report of case. Spec Care Dentist 1989; 9: 23-6.

78. Hardie J, Ringland T, Yang WH, Wagner V. Potentially fatal hereditary angioedema: a review and case report. J Can Dent Assoc 1990; 56: 1096-9.

79. Atkinson JC, Frank MM. Oral manifestations and dental management of patients with hereditary angioedema. J Oral Pathol Med 1991; 20: 139-42.

80. Hurley JE, Rayden MR. Hereditary angio-oedema in relation to dentistry. Br J Oral Surg 1978; 16: 26-30.

81. Degroote DF, Smith GL, Huttula GS. Acute airway obstruction following tooth extraction in hereditary angioedema. J Oral Maxillofac Surg 1985; 43: 52-4.

82. Starr JC, Brasher GW. Hereditary angioedema with 14-year remission. South Med J 1975; 68: 1184-5.

83. Bock SC, Skriver K, Nielson E, Thorgerson H-C, Wiman B, Donaldson VH, Eddy RL, Marrinan J, Radziewska E , Huber R, Shows TB, Magnusson S. Human C1 inhibitor:Primary structure, cDNA cloning, and chromosomal localization. Biochemistry 1986; 25: 4292-301.

84. Verpy E, Biasotto M , Brai M, Misiano G, Meo T, Tosi M. Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angioedema. Am J Hum Genet 1996; 59(2): 308-19.

85. Verpy E, Couture Tosi E, Eldering E, Lopez Trascasa M, Spath PJ, Meo T, Tosi M. Crucial residues in the carboxy-terminal end of C1 inhibitor revealed by pathogenic mutants impaired in secretion or function. J Clin Invest 1995; 95: 350-9.

86. Eldering E, Verpy E , Roem D, Meo T, Tosi M. COOH-terminal substitutions in the serpin C1 inhibitor that cause loop overinsertion and subsequent multimerization. J Biol Chem 1995; 270: 2579-87.

87. Kramer J, Rosen FS, Colten HR, Rajczy K, Strunk RC. Transinhibition of C1 Inhibitor Synthesis in Type-1 Hereditary Angioneurotic Edema. J Clin Invest 1993; 91: 1258-62.

88. Doekes G, Van-Es LA , Daha MR. C1 inactivator: its effciency as a regulator of classical complement pathway activation by soluble IgG aggregates. Imunology 1983; 49: 215-22.

89. Lachmann PJ, Rosen FS. The catabolism of C1 inhibitor and the pathogenesis of hereditary angio-edema. Acta path microbiol immunol scand 1984; 92: 35-9.

90. Willms K, Rosen FS, Donaldson VH. Observations on the ultrastructure of lesions induced in human and guinea pig skin by C 1 esterase and polypeptide from hereditary angioneurotic edema (HANE) plasma. Clin Immunol Immunopathol 1975; 4: 174-88.

91. Fields T, Ghebrehiwet B, Kaplan AP. Kinin formation in hereditary angioedema plasma: evidence against kinin derivation from C2 and in support of "spontaneous" formation of bradykinin. J Allerg Clin Immunol 1983; 72: 54-60.

92. Schapira M, Silver LD, Scott CF, Schmaier AH, Prograis LJ, Curd JG, Colman RW. Prekallikrein activation and high-molecular-weight kininogen consumption in hereditary angioedema. N Engl J Med 1983; 308: 1050-4.

93. Schapira M, de-Agostini A, Colman RW. C1 inhibitor: the predominant inhibitor of plasma kallikrein. Methods Enzymol 1988; 163: 179-85.

94. Nussberger J, Cugno M, Amstutz C, Cicardi M, Pellacani A, Agostoni A. Plasma bradykinin in angio-oedema. Lancet 1998; 351(9117): 1693-7.

95. Strang CJ, Cholin S , Spragg J, Davis AE, Schneeberger EE, Donaldson VH, Rosen FS. Angioedema induced by a peptide derived from complement component C2. J Exp Med 1988; 168: 1685-98.

96. Shoemaker LR, Schurman SJ, Donaldson VH, Davis AE. Hereditary Angioneurotic Oedema - Characterization of Plasma Kinin and Vascular Permeability-Enhancing Activities. Clin Exp Immunol 1994; 95: 22-8.

97. Hugli TE, Kawahara MS, Unson CG, Molinar-Rode R, Erickson BW. The active site of human C4a anaphylatoxin. Mol Immunol 1983; 20: 637-45.

98. Lung CC, Chan EKL, Zuraw BL. Analysis of an exon 1 polymorphism of the B2 bradykinin receptor gene and its transcript in normal subjects and patients with C1 inhibitor deficiency. J Allerg Clin Immunol 1997; 99(1): 134-46.

99. Ruddy S. Hereditary angioedema. Undersuspected, underdiagnosed. Hosp Pract Off 1988; 23: 91-6, 99-100.

100. Feller EJ, Spiro HM, Katz LA. Hereditary angioneurotic oedema: an unusual cause of recurring abdominal pain. Gut 1970; 11: 983-8.

101. Small P, Frenkiel S. Hereditary angioneurotic edema first observed as an epiglottiditis. Arch Otolaryngol 1983; 109: 195-6.

102. Morris GE, Slavin BM, Browse NL. Hereditary angioneurotic oedema: a neglected diagnosis. J Clin Pathol 1987; 40: 516-7.

103. Gjonnaess HA. Cold promoted activation of factor VII. I. Evidence for the existence of an activator. Thromb Diath Haemorrh 1972; 28 : 155-68.

104. Patston PA, Gettins P, Beechem J, Schapira M. Mechanism of serpin action: Evidence that C1 inhibitor functions as a suicide substrate. Biochemistry 1991; 30: 8876-82.

105. Donaldson VH. Cold enhancement of blood coagulation: observations on the role of C1-inhibitor. Acta path microbiol immunol scand 1984; 92: 41-7.

106. Nilsson T, Back O. On the role of C1-esterase inhibitor in cold urticaria. Acta Derm Venerol 1984; 64: 197-202.

107. VanRoyen EA, Lohmann S, Voss M, Pondmann KW. C1 inaktivator and cold-promoted activation of factor VII. J Lab Clin Med 1978; 92: 152-63.

108. Czendlik C, Lämmle B, Duckert F. Cold promoted activation and factor XII, prekallikrein and C1- inhibitor. Thromb Haemost 1985; 242-4.

109. Spath PJ, Wuthrich B. Angioedema. A review on the acquired, allergic or non-allergic, and the hereditary forms. Recenti Prog Med 1990; 81: 513-31.

110. Frank MM. Complement in the pathophysiology of human disease. N Engl J Med 1987; 316: 1525-30.

111. Alsenz J, Bork K, Loos M. Autoantibody-mediated acquired deficiency of C1 inhibitor. N Engl J Med 1987; 316: 1360-6.

112. Bork K, Alsenz J, Böckers M, Noah E, Loos M. IgG-Antikörperbildung gegen C1-Inhibitor als Ursache Lebensbedrohlicher Angioödeme. Dtsch med Wschr 1987; 112: 503-6.

113. Morrison RCA, Rabson AR. The late onset form of C1 esterase-inhibitor deficiency presenting as food allergy. J Allergy Clin Immunol 1987; 79: 336-9.

114. Malbran A, Hammer CH, Frank MM, Fries LF. Acquired angioedema: observations on the mechanism of action of autoantibodies directed against C1 esterase inhibitor. J Allergy Clin Immunol 1988; 81: 1199-204.

115. Jackson J, Sim RB, Whelan A, Feighery C. An IgG autoantibody which inactivates C1-inhibitor. Nature 1986; 323: 722-4.

116. Rodriguez M, Ancochea J, De Buen C, Merino JL, Marquës G, Vivanco F. Acquired C1-inhibitor deficiency associated with a lupus-like anticoagulant activity. Ann Allergy 1988; 61: 348-50.

117. Wozel G, Rietzschel I. Erworbener C1-Esterase-Inhibitor-Mangel, persistierende Lidoedeme und subakuter Lupus erythematodes. [Acquired deficiency of C1 esterase inhibitor, persistent eyelid edema and subacute lupus erythematosus]. Dermatol Monatsschr 1988; 174: 741-7.

118. Alsenz J, Lambris JD, Bork K, Loos M. Acquired C1 Inhibitor (C1-INH) Deficiency type II. J Clin Invest 1989; 83: 1794-9.

119. Donaldson VH, Bernstein DI, Wagner CJ, Mitchell BH, Scinto J, Bernstein IL. Angioneurotic edema with acquired C(1)bar inhibitor deficiency and autoantibody to C(1)bar inhibitor-response to plasmapheresis and cytotoxic therapy. J Lab Clin Med 1992; 119: 397-406.

120. Bain BJ, Catovsky D, Ewan PW. Acquired Angioedema as the Presenting Feature of Lymphoproliferative Disorders of Mature B-Lymphocytes. Cancer 1993; 72: 3318-22.

121. Ciaccia D, Brazer SR, Baker ME. Acquired C1 Esterase Inhibitor Deficiency Causing Intestinal Angioedema - CT Appearance - Case Report. Am J Roentgenol 1993; 161: 1215-6.

122. Cicardi M, Bisiani G, Cugno M, Spath PJ, Agostoni A. Autoimmune C1 inhibitor deficiency: report of eight patients. Am J Med 1993; 95: 169-75.

123. Delmer A, Garban F , Letourneau A, Conard J, Weiss L, Diebold J, Zittoun R. Waldenstroms Macroglobulinemia with Prominent Splenomegaly and Multiple Immune Disorders. Haematologica 1993; 78: 408-10.

124. Eck SL, Morse JH, Janssen DA, Emerson SG, Markovitz DM. Angioedema presenting as chronic gastrointestinal symptoms. Am J Gastroenterol 1993; 88: 436-9.

125. Wasserfallen JB, Spaeth P, Guillou L, Pecoud AR. Acquired deficiency in C1-inhibitor associated with signet ring cell gastric adenocarcinoma: A probable connection of antitumor- associated antibodies, hemolytic anemia, and complement turnover. J Allerg Clin Immunol 1995; 95: 124-31.

126. Jackson J, Sim RB, Whaley K, Feighery C. Autoantibody fascilitated cleavage of C1-inhibitor in autoimmune angioedema. J Clin Invest 1989; 83: 698-707.

127. Blohme G. Treatment of hereditary angioneurotic oedema with tranexamic acid. A random double-blind cross-over study. Acta med scand 1972; 192: 293-8.

128. Lundh B. Tranexamic acid in hereditary angioedema-a progress report. N Engl J Med 1973; 288: 53-.

129. Sheffer AL, Austen KF, Rosen FS. Tranexamic acid therapy in hereditary angioneurotic edema. N Engl J Med 1972; 287: 452-4.

130. Gelfand JA, Sherins RJ, Alling DW, Frank MM. Treatment of hereditary angioedema with danazol. N Engl J Med 1976; 295: 1444-8.

131. Tappeiner G, Hintner H, Glatzl J, Wolff K. Hereditary angio-oedema: treatment with danazol. Br J Dermatol 1979; 100: 207-12.

132. Gadek JE, Hosea SW , Gelfand JA, Santaella M, Wickerhauser M, Triantaphyllopoulos DC, Frank MM. Replacement therapy in hereditary angioedema. N Engl J Med 1980; 302: 542-6.

133. Rajagopal C, Harper JR. Successful use of danazol for hereditary angioedema. Arch Dis Child 1981; 56: 229-30.

134. Myreng Y, Holst T. Behandling av hereditært angioødem med danazol. Tidsskr Nor Laegeforen 1983; 103: 2050-1.

135. Zurlo JJ, Frank MM . The long-term safety of danazol in women with hereditary angioedema. Fertil steril 1990; 54: 64-72.

136. Cicardi M, Bergamaschini L, Cugno M, Hack E, Agostoni G, Agostoni A. Long-term treatment of hereditary angioedema with attenuated androgens: a survey of a 13-year experience. J Allergy Clin Immunol 1991; 87: 768-73.

137. Robinson LC, Hart LL. Danazol in Hereditary Angioedema. Ann Pharmacoter 1992; 26: 1251-2.

138. Barakat A, Castaldo AJ. Hereditary angioedema: danazol therapy in a 5-year-old child [letter]. Am J Dis Child 1993; 147: 931-2.

139. Hosea SW, Santaella ML, Brown EJ, Berger M, Katusha K, Frank MM. Long-term therapy of hereditary angioedema with danazol. Ann Int Med 1980; 93: 809-12.

140. Agostoni A, Bergamaschini L, Martignoni G, Cicardi M, Marasini B. Treatment of acute attacks of hereditary angioedema with C1- inhibitor concentrate. Ann Allergy 1980; 44: 299-301.

141. Greaves M, Lawlor F. Angioedema: manifestations and management. J Am Acad Dermatol 1991; 25: 155-61; discus.

142. Brickman CM, Frank MM, Kaliner M. Urine-histamine levels in patients with hereditary angioedema (HAE). J Allergy Clin Immunol 1988; 82: 403-6.

 

 



 
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