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43. Refractory exacerbations of hereditary angioedema with associated Helicobacter pylori infection. Rais M; Unzeitig J; Grant JA J Allergy Clin Immunol; 1999 Apr; 103(4):713-4. PubMed ID: 10200026 [No Abstract] [Full Text] [Related]
44. [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 [TBL] [Abstract][Full Text] [Related]
45. [Immunologic parameters in chronic urticaria]. Malet A; Engel P; Huguet J; García-Calderón PA Allergol Immunopathol (Madr); 1986; 14(5):375-81. PubMed ID: 3799406 [TBL] [Abstract][Full Text] [Related]
46. C1 inhibitor deficiency: molecular and immunologic basis of hereditary and acquired angioedema. Oltvai ZN; Wong EC; Atkinson JP; Tung KS Lab Invest; 1991 Oct; 65(4):381-8. PubMed ID: 1921329 [No Abstract] [Full Text] [Related]
47. The second component of complement (C2) as an index of hereditary angioneurotic edema. Sobel AT; Moisy M; Belghiti D; Gabay Y; Lagrue G J Clin Lab Immunol; 1978 Nov; 1(3):179-81. PubMed ID: 756467 [TBL] [Abstract][Full Text] [Related]
48. Immunodiffusion assay of C1 inhibitor function in serum: prospective analysis in angioedema-urticaria. Yelvington M; Prograis LJ; Pizzo CJ; Curd JG Am J Clin Pathol; 1983 Sep; 80(3):309-13. PubMed ID: 6410904 [TBL] [Abstract][Full Text] [Related]
49. Recurrent abdominal pain as the sole manifestation of hereditary angioedema in multiple family members. Weinstock LB; Kothari T; Sharma RN; Rosenfeld SI Gastroenterology; 1987 Nov; 93(5):1116-8. PubMed ID: 3653633 [TBL] [Abstract][Full Text] [Related]
50. Cleavage of the second component of complement by plasma proteases: implications in hereditary C1-inhibitor deficiency. Smith MA; Kerr MA Immunology; 1985 Nov; 56(3):561-70. PubMed ID: 2934317 [TBL] [Abstract][Full Text] [Related]
52. Hereditary angioedema: a case with ascites yet no symptoms in the family. Shinzato T; Nakamura H; Kuniyoshi T; Higashionna A; Uehara T; Oshiro J; Uechi H; Shikiya K; Sakugawa H; Kinjo F Intern Med; 1992 May; 31(5):633-5. PubMed ID: 1504426 [TBL] [Abstract][Full Text] [Related]
53. Mode of interaction of different polyanions with the first (C1, C1), the second (C2) and the fourth (C4) component of complement--I. Effect on fluid phase C1 and on C1 bound to EA or to EAC4. Raepple E; Hill HU; Loos M Immunochemistry; 1976 Mar; 13(3):251-5. PubMed ID: 1278930 [No Abstract] [Full Text] [Related]
54. [Familial studies of patients with hereditary angioedema]. Bozhkov B; Nikolov K; Baleva M Vutr Boles; 1988; 27(4):62-5. PubMed ID: 3213025 [TBL] [Abstract][Full Text] [Related]
55. [Acquired angioedema with C1-INH deficiency and accompanying chronic spontaneous urticaria in a patient with chronic lymphatic B cell leukemia]. Klossowski N; Braun SA; von Gruben V; Losem C; Plewe D; Homey B; Meller S Hautarzt; 2015 Oct; 66(10):723-5. PubMed ID: 26335859 [TBL] [Abstract][Full Text] [Related]
56. Hereditary angioedema with normal C1-inhibitor activity in women. Bork K; Barnstedt SE; Koch P; Traupe H Lancet; 2000 Jul; 356(9225):213-7. PubMed ID: 10963200 [TBL] [Abstract][Full Text] [Related]
57. Acquired C1 esterase inhibitor deficiency and angioedema: a review. Gelfand JA; Boss GR; Conley CL; Reinhart R; Frank MM Medicine (Baltimore); 1979 Jul; 58(4):321-8. PubMed ID: 449665 [TBL] [Abstract][Full Text] [Related]