658 related articles for article (PubMed ID: 17941288)
1. 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]
2. 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]
3. 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]
4. Hereditary angioedema: a Taiwanese family with a novel gene mutation.
Wen DC; Shyur SD; Wu JY; Lin CC; Chiang YC; Huang LH; Lin MT; Yang HC; Liang PH
Asian Pac J Allergy Immunol; 2007; 25(2-3):163-7. PubMed ID: 18035804
[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. Mutation screening of the C1 inhibitor gene among Hungarian patients with hereditary angioedema.
Kalmár L; Bors A; Farkas H; Vas S; Fandl B; Varga L; Füst G; Tordai A
Hum Mutat; 2003 Dec; 22(6):498. PubMed ID: 14635117
[TBL] [Abstract][Full Text] [Related]
7. Hereditary angioedema with a de novo mutation of exon 8 in the C1 inhibitor gene showing recurrent edema of the hands around the peripheral joints: importance for the differential diagnosis of joint swelling.
Sugiyama E; Ozawa T; Taki H; Maruyama M; Yamashita N; Ohta M; Hirata M; Kobayashi M
Arthritis Rheum; 2001 Apr; 44(4):974-7. PubMed ID: 11315937
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
10. 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]
11. HAEdb: a novel interactive, locus-specific mutation database for the C1 inhibitor gene.
Kalmár L; Hegedüs T; Farkas H; Nagy M; Tordai A
Hum Mutat; 2005 Jan; 25(1):1-5. PubMed ID: 15580551
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Analysis of SERPING1 expression on hereditary angioedema patients: quantitative analysis of full-length and exon 3 splicing variants.
de la Cruz RM; López-Lera A; López-Trascasa M
Immunol Lett; 2012 Jan; 141(2):158-64. PubMed ID: 22001489
[TBL] [Abstract][Full Text] [Related]
15. Hereditary angioedema: a decade of human C1-inhibitor concentrate therapy.
Farkas H; Jakab L; Temesszentandrási G; Visy B; Harmat G; Füst G; Széplaki G; Fekete B; Karádi I; Varga L
J Allergy Clin Immunol; 2007 Oct; 120(4):941-7. PubMed ID: 17761272
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. SERPING1 mutations in 59 families with hereditary angioedema.
López-Lera A; Garrido S; Roche O; López-Trascasa M
Mol Immunol; 2011 Oct; 49(1-2):18-27. PubMed ID: 21864911
[TBL] [Abstract][Full Text] [Related]
18. Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations.
Blanch A; Roche O; López-Granados E; Fontán G; López-Trascasa M
Hum Mutat; 2002 Nov; 20(5):405-6. PubMed ID: 12402344
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]