196 related articles for article (PubMed ID: 36418094)
1. A Missense Mutation of the Plasminogen Gene in a Japanese Family with Hereditary Angioedema with Normal C1 Inhibitor: Third Family Survey in Asia.
Yakushiji H; Yamagami K; Hashimura C; Iwasaki H; Horiuchi T
Intern Med; 2023 Jul; 62(13):2005-2008. PubMed ID: 36418094
[TBL] [Abstract][Full Text] [Related]
2. Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence.
Bork K; Machnig T; Wulff K; Witzke G; Prusty S; Hardt J
Orphanet J Rare Dis; 2020 Oct; 15(1):289. PubMed ID: 33059692
[TBL] [Abstract][Full Text] [Related]
3. Hereditary angioedema with a mutation in the plasminogen gene.
Bork K; Wulff K; Steinmüller-Magin L; Braenne I; Staubach-Renz P; Witzke G; Hardt J
Allergy; 2018 Feb; 73(2):442-450. PubMed ID: 28795768
[TBL] [Abstract][Full Text] [Related]
4. A missense mutation in the plasminogen gene, within the plasminogen kringle 3 domain, in hereditary angioedema with normal C1 inhibitor.
Dewald G
Biochem Biophys Res Commun; 2018 Mar; 498(1):193-198. PubMed ID: 29548426
[TBL] [Abstract][Full Text] [Related]
5. Gene Mutations Linked to Hereditary Angioedema in Solitary Angioedema Patients With Normal C1 Inhibitor.
Bork K; Wulff K; Witzke G; Staubach P; Hardt J; Meinke P
J Allergy Clin Immunol Pract; 2023 Aug; 11(8):2441-2449. PubMed ID: 36787826
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene.
Bork K; Wulff K; Witzke G; Machnig T; Hardt J
Orphanet J Rare Dis; 2020 Feb; 15(1):52. PubMed ID: 32066472
[TBL] [Abstract][Full Text] [Related]
9. Inheritance Pattern of Hereditary Angioedema Indicates Mutation-Dependent Selective Effects During Early Embryonic Development.
Bork K; Wulff K; Witzke G; Hardt J; Meinke P
J Allergy Clin Immunol Pract; 2022 Apr; 10(4):1029-1037. PubMed ID: 34890828
[TBL] [Abstract][Full Text] [Related]
10. Hereditary Angioedema: Diagnosis, Clinical Implications, and Pathophysiology.
Sinnathamby ES; Issa PP; Roberts L; Norwood H; Malone K; Vemulapalli H; Ahmadzadeh S; Cornett EM; Shekoohi S; Kaye AD
Adv Ther; 2023 Mar; 40(3):814-827. PubMed ID: 36609679
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Mutant plasminogen in hereditary angioedema is bypassing FXII/kallikrein to generate bradykinin.
Hintze S; Möhl BS; Beyerl J; Wulff K; Wieser A; Bork K; Meinke P
Front Physiol; 2022; 13():1090732. PubMed ID: 36685169
[TBL] [Abstract][Full Text] [Related]
13. Angioedema Without Wheals: Challenges in Laboratorial Diagnosis.
Grumach AS; Veronez CL; Csuka D; Farkas H
Front Immunol; 2021; 12():785736. PubMed ID: 34956216
[TBL] [Abstract][Full Text] [Related]
14. Hereditary angio-oedema with normal C1-INH, developing recurrent acute abdomen after taking low-dose oestrogen-progestin: A case report.
Nakayama T; Tamimoto Y; Shimomura Y; Tsukamoto H
Mod Rheumatol Case Rep; 2023 Jun; 7(2):491-494. PubMed ID: 36928504
[TBL] [Abstract][Full Text] [Related]
15. Pathophysiology of Hereditary Angioedema (HAE) Beyond the SERPING1 Gene.
Sharma J; Jindal AK; Banday AZ; Kaur A; Rawat A; Singh S; Longhurst H
Clin Rev Allergy Immunol; 2021 Jun; 60(3):305-315. PubMed ID: 33442779
[TBL] [Abstract][Full Text] [Related]
16. Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations.
Bork K; Wulff K; Witzke G; Hardt J
Allergy; 2015 Aug; 70(8):1004-12. PubMed ID: 25952149
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Hereditary angioedema with normal C1 inhibitor: clinical characteristics and treatment response with plasma-derived human C1 inhibitor concentrate (Berinert
Bouillet L; Boccon-Gibod I; Gompel A; Floccard B; Martin L; Blanchard-Delaunay C; Launay D; Fain O
Eur J Dermatol; 2017 Apr; 27(2):155-159. PubMed ID: 28251901
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Biochemistry, molecular genetics, and clinical aspects of hereditary angioedema with and without C1 inhibitor deficiency.
Miyata T; Horiuchi T
Allergol Int; 2023 Jul; 72(3):375-384. PubMed ID: 37169642
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]