583 related articles for article (PubMed ID: 10984376)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. [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]
8. First case of homozygous C1 inhibitor deficiency.
Blanch A; Roche O; Urrutia I; Gamboa P; Fontán G; López-Trascasa M
J Allergy Clin Immunol; 2006 Dec; 118(6):1330-5. PubMed ID: 17137866
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Five novel mutations in the C1 inhibitor gene (C1NH) leading to a premature stop codon in patients with type I hereditary angioedema.
Freiberger T; Kolárová L; Mejstrík P; Vyskocilová M; Kuklínek P; Litzman J
Hum Mutat; 2002 Apr; 19(4):461. PubMed ID: 11933207
[TBL] [Abstract][Full Text] [Related]
11. Unique C1 inhibitor dysfunction in a kindred without angioedema. I. A mutant C1 INH that inhibits C1-s but not C1-r.
Wisnieski JJ; Knauss TC; Yike I; Dearborn DG; Narvy RL; Naff GB
J Immunol; 1994 Mar; 152(6):3199-209. PubMed ID: 8144914
[TBL] [Abstract][Full Text] [Related]
12. [Identification of a novel mutation of C1 inhibitor gene in a Chinese family with hereditary angioedema].
Zhi YX; Zhang HY; Huang SZ
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Dec; 25(6):664-6. PubMed ID: 14714307
[TBL] [Abstract][Full Text] [Related]
13. Immunoblotting of plasma in a pregnant patient with hereditary angioedema.
Chhibber G; Cohen A; Lane S; Farber A; Meloni FJ; Schmaier AH
J Lab Clin Med; 1990 Jan; 115(1):112-21. PubMed ID: 1688910
[TBL] [Abstract][Full Text] [Related]
14. Detection of C1 inhibitor mutations in patients with hereditary angioedema.
Zuraw BL; Herschbach J
J Allergy Clin Immunol; 2000 Mar; 105(3):541-6. PubMed ID: 10719305
[TBL] [Abstract][Full Text] [Related]
15. Molecular diagnosis and management of hereditary angioedema in a Greek family.
Papadopoulou-Alataki E; Foerster T; Antari V; Pavlitou-Tsiontsi A; Varlamis G
Int Arch Allergy Immunol; 2008; 147(2):166-70. PubMed ID: 18535392
[TBL] [Abstract][Full Text] [Related]
16. The pathophysiology of hereditary angioedema.
Davis AE
Clin Immunol; 2005 Jan; 114(1):3-9. PubMed ID: 15596403
[TBL] [Abstract][Full Text] [Related]
17. Hereditary angioedema: a study of three families.
Pola J; Valdivieso R; Zapata C; Carrillo T; Moneo I; Hinojosa M; Losada E
Allergol Immunopathol (Madr); 1987; 15(6):375-8. PubMed ID: 3445878
[TBL] [Abstract][Full Text] [Related]
18. Novel and recurrent mutations in the C1NH gene of Arab patients affected with hereditary angioedema.
Faiyaz-Ul-Haque M; Al-Gazlan S; Abalkhail HA; Al-Abdulatif A; Toulimat M; Peltekova I; Khaliq AM; Al-Dayel F; Zaidi SH
Int Arch Allergy Immunol; 2010; 151(2):149-54. PubMed ID: 19752569
[TBL] [Abstract][Full Text] [Related]
19. Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor.
Dewald G; Bork K
Biochem Biophys Res Commun; 2006 May; 343(4):1286-9. PubMed ID: 16638441
[TBL] [Abstract][Full Text] [Related]
20. Coagulation Factor XII Gene Mutation in Brazilian Families with Hereditary Angioedema with Normal C1 Inhibitor.
Moreno AS; Valle SO; Levy S; França AT; Serpa FS; Arcuri HA; Palma MS; Campos WN; Dias MM; Ponard D; Monnier N; Lunardi J; Bork K; Silva WA; Arruda LK
Int Arch Allergy Immunol; 2015; 166(2):114-20. PubMed ID: 25790805
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
