These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
192 related articles for article (PubMed ID: 861073)
1. [Study by means of enzymatic and immunochemical determination of Cl esterase inhibitor in 59 patients with hereditary angioneurotic edema]. Agostoni A; Marasini B; Cicardi M; Martignoni G; Brenna O Boll Ist Sieroter Milan; 1977 Mar; 56(1):22-8. PubMed ID: 861073 [TBL] [Abstract][Full Text] [Related]
2. [New preparation method of C1 esterase for the dosage of its plasma inhibitor]. Gozin D; Ollier-Hartmann MP; Lerable J; Hartmann L; Soulier JP Biomed Pharmacother; 1983; 37(5):228-30. PubMed ID: 6607074 [TBL] [Abstract][Full Text] [Related]
3. [Abdominal manifestations of hereditary angioneurotic edema. Importance of the exploration of the complement system (apropos of 29 families)]. Hartmann L; Brecy H; Griffe J Biomedicine; 1976 Dec; 24(6):443-9. PubMed ID: 1022317 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Clinical studies of sudden upper airway obstruction in patients with hereditary angioedema due to C1 esterase inhibitor deficiency. Bork K; Hardt J; Schicketanz KH; Ressel N Arch Intern Med; 2003 May; 163(10):1229-35. PubMed ID: 12767961 [TBL] [Abstract][Full Text] [Related]
14. Distinction between hereditary and acquired angioneurotic oedema according to the complement system. Brecy H; Hartmann L Biomedicine; 1975 Oct; 23(8):328-34. PubMed ID: 1231927 [TBL] [Abstract][Full Text] [Related]
15. Normal C1 inhibitor mRNA expression level in type I hereditary angioedema patients: newly found C1 inhibitor gene mutations. Kang HR; Yim EY; Oh SY; Chang YS; Kim YK; Cho SH; Min KU; Kim YY Allergy; 2006 Feb; 61(2):260-4. PubMed ID: 16409206 [TBL] [Abstract][Full Text] [Related]
16. [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]
17. [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]
18. [Anomaly of the polypeptide and oligosaccharide chains of alpha-2-neuraminoglycoprotein in various types of hereditary angioneurotic edema]. Ollier-Hartmann MP; Hartmann L C R Seances Acad Sci D; 1980 May; 290(18):1201-4. PubMed ID: 6772326 [TBL] [Abstract][Full Text] [Related]
19. Hereditary angioedema: case report of a family. Yilmaz M; Kendirli SG; Altintaş D; Bingöl G Turk J Pediatr; 2000; 42(3):230-3. PubMed ID: 11105624 [TBL] [Abstract][Full Text] [Related]
20. [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] [Next] [New Search]