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2. [A case report of hereditary angioedema and studies on the serum components of complement, C1-inactivator and proteinase inhibitors during edema attack]. Mikami A; Kohno M Hokkaido Igaku Zasshi; 1987 May; 62(3):497-500. PubMed ID: 3610041 [TBL] [Abstract][Full Text] [Related]
3. [Hereditary angioedema caused by a deficiency of C1 esterase inhibitor. A sporadic case of late appearance]. Verea Hernando HR; Domínguez Juncal LM; Masa Jiménez JF; Martín Egana MT; Ferreiro Arias M; Fontán Bueso JM Med Clin (Barc); 1983 Dec; 81(19):880. PubMed ID: 6656470 [No Abstract] [Full Text] [Related]
4. [Determination of inhibitor of the first component of complement (C1 INH) in patients with hereditary angioedema]. Rivero S; Gajardo M; Guzmán L Rev Med Chil; 1982 May; 110(5):444-8. PubMed ID: 6819622 [No Abstract] [Full Text] [Related]
5. [Profile of the complement system in a family with hereditary angioedema]. Rivero S; Guzmán L Rev Med Chil; 1983 Nov; 111(11):1111-6. PubMed ID: 6431574 [No Abstract] [Full Text] [Related]
6. [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; 299(16):667-9. PubMed ID: 6440668 [TBL] [Abstract][Full Text] [Related]
7. [Hereditary angioedema (with an analysis of 22 cases from 6 families)]. Zhang HY Zhonghua Yi Xue Za Zhi; 1985 Mar; 65(3):156-9. PubMed ID: 3928116 [No Abstract] [Full Text] [Related]
8. [Hereditary angioedema. A clinical and immunologic contribution based on our 8 clinical cases under long-term treatment with androgens]. Zimmermann HP; Wüthrich B; Späth P Schweiz Med Wochenschr; 1983 Jun; 113(24):876-84. PubMed ID: 6879139 [TBL] [Abstract][Full Text] [Related]
9. Modulation of the antigenicity of C1r and C1s by C1 inactivator. Ziccardi RJ; Cooper NR J Immunol; 1978 Dec; 121(6):2148-52. PubMed ID: 722073 [No Abstract] [Full Text] [Related]
10. The effect of synthetic androgens in hereditary angioneurotic edema: alteration of C1 inhibitor and C4 levels. Rosse WF; Logue GL; Silberman HR; Frank MM Trans Assoc Am Physicians; 1976; 89():122-32. PubMed ID: 1020118 [No Abstract] [Full Text] [Related]
11. Hereditary angioedema in Czechoslovakia. Clinical, immunological, genetic and therapeutic studies of 16 families. Starsia Z; Hegyi E; Kuklinek P; Cáp J; Stefanovic J; Lokaj J Allerg Immunol (Leipz); 1988; 34(1):35-42. PubMed ID: 3400559 [TBL] [Abstract][Full Text] [Related]
12. Complement components in hereditary angioedema and chronic urticaria. Laurell AB; Mårtensson U; Sjöholm AG Int Arch Allergy Appl Immunol; 1975; 49(1-2):86-8. PubMed ID: 124709 [No Abstract] [Full Text] [Related]
13. [Hereditary angioedema: description of a sibship and review]. Matter L; Schopfer K; Voegelin HP; Fueter R Schweiz Med Wochenschr; 1981 Aug; 111(34):1238-45. PubMed ID: 6974398 [TBL] [Abstract][Full Text] [Related]
15. A sensitive colorimetric method for the measurement of serum C1 inactivator using the substrate N-alpha-acetyl-L-lysine methyl ester. Harpel PC J Immunol; 1970 Apr; 104(4):1024-30. PubMed ID: 5429516 [No Abstract] [Full Text] [Related]
16. [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]
17. Hereditary angioedema: diagnosis and management. Chng HH; Boey ML Singapore Med J; 1990 Apr; 31(2):177-9. PubMed ID: 2371584 [TBL] [Abstract][Full Text] [Related]
18. [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; 129(7):285-91. PubMed ID: 10093876 [TBL] [Abstract][Full Text] [Related]
19. [A case of hereditary angioedema]. Tarallo MR; Vollono C; Inserra C; Langella G; Tarallo S; Grandi E Pediatr Med Chir; 1994; 16(3):297-9. PubMed ID: 7971458 [TBL] [Abstract][Full Text] [Related]
20. Hereditary angioedema. Report of a large kindred with a rare genetic variant of C1-esterase inhibitor. Jacot-Guillarmod H; Carbonara AO; De Marchi M; Ressa TG Quad Sclavo Diagn; 1973 Mar; 9(1):159-65. PubMed ID: 4132954 [No Abstract] [Full Text] [Related] [Next] [New Search]