BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 33508266)

  • 1. Novel hereditary angioedema linked with a heparan sulfate 3-O-sulfotransferase 6 gene mutation.
    Bork K; Wulff K; Möhl BS; Steinmüller-Magin L; Witzke G; Hardt J; Meinke P
    J Allergy Clin Immunol; 2021 Oct; 148(4):1041-1048. PubMed ID: 33508266
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. The Expanding Spectrum of Mutations in Hereditary Angioedema.
    Veronez CL; Csuka D; Sheikh FR; Zuraw BL; Farkas H; Bork K
    J Allergy Clin Immunol Pract; 2021 Jun; 9(6):2229-2234. PubMed ID: 33746090
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Phenotypic and Genotypic Characterization of Hereditary Angioedema in Saudi Arabia.
    Sheikh F; Alajlan H; Albanyan M; Alruwaili H; Alawami F; Sumayli S; Al Gazlan S; Abu Awwad S; Al-Dhekri H; Al-Saud B; Arnaout R; Alrayes H; Sayes N; Al-Hamed MH; Al-Mousa H; AlShareef S; Alazami AM
    J Clin Immunol; 2023 Feb; 43(2):479-484. PubMed ID: 36348183
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel SERPING1 mutations and genetic factors modifying the clinical phenotype.
    Grivčeva-Panovska V; Košnik M; Korošec P; Andrejević S; Karadža-Lapić L; Rijavec M
    Ann Med; 2018 May; 50(3):269-276. PubMed ID: 29513108
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema.
    Bafunno V; Firinu D; D'Apolito M; Cordisco G; Loffredo S; Leccese A; Bova M; Barca MP; Santacroce R; Cicardi M; Del Giacco S; Margaglione M
    J Allergy Clin Immunol; 2018 Mar; 141(3):1009-1017. PubMed ID: 28601681
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families.
    Veronez CL; Moreno AS; Constantino-Silva RN; Maia LSM; Ferriani MPL; Castro FFM; Valle SR; Nakamura VK; Cagini N; Gonçalves RF; Mansour E; Serpa FS; Coelho Dias GA; Piccirillo MA; Toledo E; de Souza Bernardes M; Cichon S; Stieber C; Arruda LK; Pesquero JB; Grumach AS
    J Allergy Clin Immunol Pract; 2018; 6(4):1209-1216.e8. PubMed ID: 29128335
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Frequent life-threatening laryngeal attacks in two Croatian families with hereditary angioedema due to C1 inhibitor deficiency harbouring a novel frameshift mutation in SERPING1.
    Karadža-Lapić L; Korošec P; Šilar M; Košnik M; Cikojević D; Lozić B; Rijavec M
    Ann Med; 2016 Nov; 48(7):485-491. PubMed ID: 27187751
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.