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2. [Recurrent attacks of angioedema ascribed to the use of estrogen preparations and a pregnancy (hereditary angioedema type 3)]. van der Klooster JM; Schelfhout LJ; Grootendorst AF; Zweers PG Ned Tijdschr Geneeskd; 2002 Aug; 146(34):1599-602. PubMed ID: 12224485 [TBL] [Abstract][Full Text] [Related]
3. C1-inhibitor deficiencies (hereditary angioedema): where are we with therapies? Lock RJ; Gompels MM Curr Allergy Asthma Rep; 2007 Jul; 7(4):264-9. PubMed ID: 17547847 [TBL] [Abstract][Full Text] [Related]
5. Clinical, biochemical, and genetic characterization of a novel estrogen-dependent inherited form of angioedema. Binkley KE; Davis A J Allergy Clin Immunol; 2000 Sep; 106(3):546-50. PubMed ID: 10984376 [TBL] [Abstract][Full Text] [Related]
6. Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course. Bork K; Gül D; Hardt J; Dewald G Am J Med; 2007 Nov; 120(11):987-92. PubMed ID: 17976427 [TBL] [Abstract][Full Text] [Related]
7. The C1 inhibitor deficiency. A review. Carreer FM Eur J Clin Chem Clin Biochem; 1992 Dec; 30(12):793-807. PubMed ID: 1489854 [TBL] [Abstract][Full Text] [Related]
8. Altered C1 inhibitor genes in type I hereditary angioedema. Stoppa-Lyonnet D; Tosi M; Laurent J; Sobel A; Lagrue G; Meo T N Engl J Med; 1987 Jul; 317(1):1-6. PubMed ID: 3587308 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. C1-inhibitor in hereditary angioneurotic edema: types I and II. Donaldson VH Behring Inst Mitt; 1989 Jul; (84):151-60. PubMed ID: 2679530 [No Abstract] [Full Text] [Related]
11. 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]
12. [C1 inhibitor deficiency. Heredity and acquired forms. Symptoms, diagnostic and therapeutic problems]. Obtułowicz K; Kapusta M; Obtułowicz A; Mazurkiewicz A Przegl Lek; 2002; 59(6):438-41. PubMed ID: 12418282 [TBL] [Abstract][Full Text] [Related]
13. C1 inhibitor and hereditary angioneurotic edema. Davis AE Annu Rev Immunol; 1988; 6():595-628. PubMed ID: 3289579 [No Abstract] [Full Text] [Related]
14. A novel RNA splice site mutation in the C1 inhibitor gene of a patient with type I hereditary angioedema. Sekijima Y; Hashimoto T; Kawachi Y; Koshihara H; Otsuka F; Ikeda S Intern Med; 2004 Mar; 43(3):253-5. PubMed ID: 15098611 [TBL] [Abstract][Full Text] [Related]
15. Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond. Agostoni A; Aygören-Pürsün E; Binkley KE; Blanch A; Bork K; Bouillet L; Bucher C; Castaldo AJ; Cicardi M; Davis AE; De Carolis C; Drouet C; Duponchel C; Farkas H; Fáy K; Fekete B; Fischer B; Fontana L; Füst G; Giacomelli R; Gröner A; Hack CE; Harmat G; Jakenfelds J; Juers M; Kalmár L; Kaposi PN; Karádi I; Kitzinger A; Kollár T; Kreuz W; Lakatos P; Longhurst HJ; Lopez-Trascasa M; Martinez-Saguer I; Monnier N; Nagy I; Németh E; Nielsen EW; Nuijens JH; O'grady C; Pappalardo E; Penna V; Perricone C; Perricone R; Rauch U; Roche O; Rusicke E; Späth PJ; Szendei G; Takács E; Tordai A; Truedsson L; Varga L; Visy B; Williams K; Zanichelli A; Zingale L J Allergy Clin Immunol; 2004 Sep; 114(3 Suppl):S51-131. PubMed ID: 15356535 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Hereditary angioedema. A report of a case and literature review]. Jiménez Saab N; Gómez Vera J; López Tiro J; Nieto Martínez S; Pliego Reyes C Rev Alerg Mex; 2006; 53(1):34-41. PubMed ID: 16634360 [TBL] [Abstract][Full Text] [Related]
18. Frequent life-threatening laryngeal attacks in two Croatian families with hereditary angioedema due to C1 inhibitor deficiency harbouring a novel frameshift mutation in SERPING1. Karadža-Lapić L; Korošec P; Šilar M; Košnik M; Cikojević D; Lozić B; Rijavec M Ann Med; 2016 Nov; 48(7):485-491. PubMed ID: 27187751 [TBL] [Abstract][Full Text] [Related]
19. A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family. Ferraro MF; Moreno AS; Castelli EC; Donadi EA; Palma MS; Arcuri HA; Lange AP; Bork K; Sarti W; Arruda LK Allergy; 2011 Oct; 66(10):1384-90. PubMed ID: 21623829 [TBL] [Abstract][Full Text] [Related]