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.
174 related articles for article (PubMed ID: 8450054)
1. Transinhibition of C1 inhibitor synthesis in type I hereditary angioneurotic edema. Kramer J; Rosen FS; Colten HR; Rajczy K; Strunk RC J Clin Invest; 1993 Mar; 91(3):1258-62. PubMed ID: 8450054 [TBL] [Abstract][Full Text] [Related]
2. Synthesis of C1 inhibitor in fibroblasts from patients with type I and type II hereditary angioneurotic edema. Kramer J; Katz Y; Rosen FS; Davis AE; Strunk RC J Clin Invest; 1991 May; 87(5):1614-20. PubMed ID: 1902490 [TBL] [Abstract][Full Text] [Related]
3. Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema. Cicardi M; Igarashi T; Rosen FS; Davis AE J Clin Invest; 1987 Mar; 79(3):698-702. PubMed ID: 3818946 [TBL] [Abstract][Full Text] [Related]
4. Impaired production of both normal and mutant C1 inhibitor proteins in type I hereditary angioedema with a duplication in exon 8. Ernst SC; Circolo A; Davis AE; Gheesling-Mullis K; Fliesler M; Strunk RC J Immunol; 1996 Jul; 157(1):405-10. PubMed ID: 8683145 [TBL] [Abstract][Full Text] [Related]
5. Type I C1 inhibitor deficiency with a small messenger RNA resulting from deletion of one exon. Ariga T; Igarashi T; Ramesh N; Parad R; Cicardi M; Davis AE J Clin Invest; 1989 Jun; 83(6):1888-93. PubMed ID: 2723063 [TBL] [Abstract][Full Text] [Related]
6. Behavior in vivo of normal and dysfunctional C1 inhibitor in normal subjects and patients with hereditary angioneurotic edema. Quastel M; Harrison R; Cicardi M; Alper CA; Rosen FS J Clin Invest; 1983 Apr; 71(4):1041-6. PubMed ID: 6833491 [TBL] [Abstract][Full Text] [Related]
7. Restriction fragment length polymorphism of the C1 inhibitor gene in hereditary angioneurotic edema. Cicardi M; Igarashi T; Kim MS; Frangi D; Agostoni A; Davis AE J Clin Invest; 1987 Dec; 80(6):1640-3. PubMed ID: 2890659 [TBL] [Abstract][Full Text] [Related]
8. Hereditary and acquired deficiencies of C1 inhibitor. Davis AE Immunodefic Rev; 1989; 1(3):207-26. PubMed ID: 2698641 [TBL] [Abstract][Full Text] [Related]
9. Plasma levels of C1- inhibitor complexes and cleaved C1- inhibitor in patients with hereditary angioneurotic edema. Cugno M; Nuijens J; Hack E; Eerenberg A; Frangi D; Agostoni A; Cicardi M J Clin Invest; 1990 Apr; 85(4):1215-20. PubMed ID: 2318974 [TBL] [Abstract][Full Text] [Related]
10. Paternal mosaicism and hereditary angioedema in a Taiwanese family. Yu TC; Shyur SD; Huang LH; Wen DC; Li JS Ann Allergy Asthma Immunol; 2007 Oct; 99(4):375-9. PubMed ID: 17941288 [TBL] [Abstract][Full Text] [Related]
11. A de novo deletion in the C1 inhibitor gene in a case of sporadic hereditary angioneurotic edema. Ariga T; Hoshioka A; Kohno Y; Sakamaki T; Matsumoto S Clin Immunol Immunopathol; 1993 Oct; 69(1):103-5. PubMed ID: 8403537 [TBL] [Abstract][Full Text] [Related]
12. C1 inhibitor gene expression in patients with hereditary angioedema: quantitative evaluation by means of real-time RT-PCR. Pappalardo E; Zingale LC; Cicardi M J Allergy Clin Immunol; 2004 Sep; 114(3):638-44. PubMed ID: 15356570 [TBL] [Abstract][Full Text] [Related]
13. Dysfunctional C1 inhibitor Ta: deletion of Lys-251 results in acquisition of an N-glycosylation site. Parad RB; Kramer J; Strunk RC; Rosen FS; Davis AE Proc Natl Acad Sci U S A; 1990 Sep; 87(17):6786-90. PubMed ID: 2118657 [TBL] [Abstract][Full Text] [Related]
14. Mutations in the C1 inhibitor gene that result in hereditary angioneurotic edema. Davis AE; Bissler JJ; Cicardi M Behring Inst Mitt; 1993 Dec; (93):313-20. PubMed ID: 8172583 [TBL] [Abstract][Full Text] [Related]