174 related articles for article (PubMed ID: 34890828)
21. Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema.
Deroux A; Boccon-Gibod I; Fain O; Pralong P; Ollivier Y; Pagnier A; Djenouhat K; Du-Thanh A; Gompel A; Faisant C; Launay D; Bouillet L
Clin Exp Immunol; 2016 Sep; 185(3):332-7. PubMed ID: 27271546
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Definition and classification of hereditary angioedema.
Proper SP; Lavery WJ; Bernstein JA
Allergy Asthma Proc; 2020 Nov; 41(Suppl 1):S03-S07. PubMed ID: 33109317
[TBL] [Abstract][Full Text] [Related]
24. Pathogenic mechanisms of bradykinin mediated diseases: dysregulation of an innate inflammatory pathway.
Kaplan AP; Joseph K
Adv Immunol; 2014; 121():41-89. PubMed ID: 24388213
[TBL] [Abstract][Full Text] [Related]
25. Screening for Plasminogen Mutations in Hereditary Angioedema Patients.
Farkas H; Dóczy A; Szabó E; Varga L; Csuka D
Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33799813
[TBL] [Abstract][Full Text] [Related]
26. Impaired control of the contact system in hereditary angioedema with normal C1-inhibitor.
Bova M; Suffritti C; Bafunno V; Loffredo S; Cordisco G; Del Giacco S; De Pasquale TMA; Firinu D; Margaglione M; Montinaro V; Petraroli A; Radice A; Brussino L; Zanichelli A; Zoli A; Cicardi M
Allergy; 2020 Jun; 75(6):1394-1403. PubMed ID: 31860755
[TBL] [Abstract][Full Text] [Related]
27. The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency.
Rupar N; Šelb J; Košnik M; Zidarn M; Andrejević S; Čulav L; Grivčeva-Panovska V; Korošec P; Rijavec M
Gene; 2024 Aug; 919():148496. PubMed ID: 38679185
[TBL] [Abstract][Full Text] [Related]
28. Deficiency of plasminogen activator inhibitor 2 in plasma of patients with hereditary angioedema with normal C1 inhibitor levels.
Joseph K; Tholanikunnel BG; Wolf B; Bork K; Kaplan AP
J Allergy Clin Immunol; 2016 Jun; 137(6):1822-1829.e1. PubMed ID: 26395818
[TBL] [Abstract][Full Text] [Related]
29. Hereditary and acquired angioedema.
Patel G; Pongracic JA
Allergy Asthma Proc; 2019 Nov; 40(6):441-445. PubMed ID: 31690390
[TBL] [Abstract][Full Text] [Related]
30. C1-inhibitor polymers activate the FXII-dependent kallikrein-kinin system: Implication for a role in hereditary angioedema.
Madsen DE; Sidelmann JJ; Biltoft D; Gram J; Hansen S
Biochim Biophys Acta; 2015 Jun; 1850(6):1336-42. PubMed ID: 25800206
[TBL] [Abstract][Full Text] [Related]
31. Hereditary angioedema in a single family with specific mutations in both plasminogen and SERPING1 genes.
Bork K; Zibat A; Ferrari DM; Wollnik B; Schön MP; Wulff K; Lippert U
J Dtsch Dermatol Ges; 2020 Mar; 18(3):215-223. PubMed ID: 32065705
[TBL] [Abstract][Full Text] [Related]
32. Analysis of cold activation of the contact system in hereditary angioedema with normal C1 inhibitor.
Larrauri B; Hester CG; Jiang H; Miletic VD; Malbran A; Bork K; Kaplan A; Frank M
Mol Immunol; 2021 Aug; 136():150-160. PubMed ID: 34153620
[TBL] [Abstract][Full Text] [Related]
33. Hereditary angioedema: Pathophysiology (HAE type I, HAE type II, and HAE nC1-INH).
Wedner HJ
Allergy Asthma Proc; 2020 Nov; 41(Suppl 1):S14-S17. PubMed ID: 33109319
[TBL] [Abstract][Full Text] [Related]
34. A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency.
Vatsiou S; Zamanakou M; Loules G; Psarros F; Parsopoulou F; Csuka D; Valerieva A; Staevska M; Porebski G; Obtulowicz K; Magerl M; Maurer M; Speletas M; Farkas H; Germenis AE
Allergol Int; 2020 Jul; 69(3):443-449. PubMed ID: 31959500
[TBL] [Abstract][Full Text] [Related]
35. Hereditary and acquired C1-inhibitor-dependent angioedema: from pathophysiology to treatment.
Zeerleder S; Levi M
Ann Med; 2016; 48(4):256-67. PubMed ID: 27018196
[TBL] [Abstract][Full Text] [Related]
36. Unnecessary Abdominal Surgeries in Attacks of Hereditary Angioedema with Normal C1 Inhibitor.
Gutierrez M; Veronez CL; Rodrigues Valle SO; Gonçalves RF; Ferriani MPL; Moreno AS; Arruda LK; Aun MV; Giavina-Bianchi P; Alonso MLO; Pesquero JB; Grumach AS
Clin Rev Allergy Immunol; 2021 Aug; 61(1):60-65. PubMed ID: 33755867
[TBL] [Abstract][Full Text] [Related]
37. Treatment of Hereditary Angioedema.
Caballero T
J Investig Allergol Clin Immunol; 2021 Feb; 31(1):1-16. PubMed ID: 33602658
[TBL] [Abstract][Full Text] [Related]
38. The Genetics of Hereditary Angioedema: A Review.
Santacroce R; D'Andrea G; Maffione AB; Margaglione M; d'Apolito M
J Clin Med; 2021 May; 10(9):. PubMed ID: 34065094
[TBL] [Abstract][Full Text] [Related]
39. Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: functional and structural correlates.
Pappalardo E; Caccia S; Suffritti C; Tordai A; Zingale LC; Cicardi M
Mol Immunol; 2008 Aug; 45(13):3536-44. PubMed ID: 18586324
[TBL] [Abstract][Full Text] [Related]
40. sgp120 and the contact system in hereditary angioedema: A diagnostic tool in HAE with normal C1 inhibitor.
Larrauri B; Hester CG; Jiang H; Miletic VD; Malbran A; Bork K; Kaplan A; Frank M
Mol Immunol; 2020 Mar; 119():27-34. PubMed ID: 31955064
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
