364 related articles for article (PubMed ID: 1489854)
1. 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]
2. Hereditary and acquired deficiencies of C1 inhibitor.
Davis AE
Immunodefic Rev; 1989; 1(3):207-26. PubMed ID: 2698641
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. Autoantibody-mediated acquired deficiency of C1 inhibitor.
Alsenz J; Bork K; Loos M
N Engl J Med; 1987 May; 316(22):1360-6. PubMed ID: 3494945
[TBL] [Abstract][Full Text] [Related]
5. Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations.
Wagenaar-Bos IG; Drouet C; Aygören-Pursun E; Bork K; Bucher C; Bygum A; Farkas H; Fust G; Gregorek H; Hack CE; Hickey A; Joller-Jemelka HI; Kapusta M; Kreuz W; Longhurst H; Lopez-Trascasa M; Madalinski K; Naskalski J; Nieuwenhuys E; Ponard D; Truedsson L; Varga L; Nielsen EW; Wagner E; Zingale L; Cicardi M; van Ham SM
J Immunol Methods; 2008 Sep; 338(1-2):14-20. PubMed ID: 18655790
[TBL] [Abstract][Full Text] [Related]
6. Autoantibody facilitated cleavage of C1-inhibitor in autoimmune angioedema.
Jackson J; Sim RB; Whaley K; Feighery C
J Clin Invest; 1989 Feb; 83(2):698-707. PubMed ID: 2536404
[TBL] [Abstract][Full Text] [Related]
7. The acquired C1-INH deficiencies with autoantibodies (AAE type II).
Alsenz J; Loos M
Behring Inst Mitt; 1989 Jul; (84):165-72. PubMed ID: 2679532
[TBL] [Abstract][Full Text] [Related]
8. A new type of acquired C1 inhibitor deficiency associated with systemic lupus erythematosus.
Cacoub P; Frémeaux-Bacchi V; De Lacroix I; Guillien F; Kahn MF; Kazatchkine MD; Godeau P; Piette JC
Arthritis Rheum; 2001 Aug; 44(8):1836-40. PubMed ID: 11508436
[TBL] [Abstract][Full Text] [Related]
9. Symptoms, course, and complications of abdominal attacks in hereditary angioedema due to C1 inhibitor deficiency.
Bork K; Staubach P; Eckardt AJ; Hardt J
Am J Gastroenterol; 2006 Mar; 101(3):619-27. PubMed ID: 16464219
[TBL] [Abstract][Full Text] [Related]
10. [Angioedema due to acquired complement-C1-inhibitor deficiency in a female patient with non-Hodgkin lymphoma and autoimmune hemolytic anemia].
Beretta KR; Späth PJ; Pedrazzini A; Martinelli G; Cavalli F
Schweiz Med Wochenschr; 1991 Jun; 121(25):943-7. PubMed ID: 1862309
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Response of variant hereditary angioedema phenotypes to danazol therapy. Genetic implications.
Gadek JE; Hosea SW; Gelfand JA; Frank MM
J Clin Invest; 1979 Jul; 64(1):280-6. PubMed ID: 376558
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. [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]
16. Autoantibodies and lymphoproliferative diseases in acquired C1-inhibitor deficiencies.
Cicardi M; Zingale LC; Pappalardo E; Folcioni A; Agostoni A
Medicine (Baltimore); 2003 Jul; 82(4):274-81. PubMed ID: 12861105
[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. [Deficiencies of C1 inhibitor: hereditary and acquired angioedema].
Porcel-Pérez JM; López-Trascasa M
Rev Clin Esp; 1996 Mar; 196 Spec No():26-30. PubMed ID: 9206804
[No Abstract] [Full Text] [Related]
19. Unmasking of acquired autoimmune C1-inhibitor deficiency by an angiotensin-converting enzyme inhibitor.
Kleiner GI; Giclas P; Stadtmauer G; Cunningham-Rundles C
Ann Allergy Asthma Immunol; 2001 Apr; 86(4):461-4. PubMed ID: 11345293
[TBL] [Abstract][Full Text] [Related]
20. Acquired C1-inhibitor deficiency.
Frank M
Behring Inst Mitt; 1989 Jul; (84):161-4. PubMed ID: 2679531
[No Abstract] [Full Text] [Related]
[Next] [New Search]