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Journal Abstract Search

237 related items for PubMed ID: 32065705

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  • 5. 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
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  • 6. 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
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  • 8. Screening for Plasminogen Mutations in Hereditary Angioedema Patients.
    Farkas H, Dóczy A, Szabó E, Varga L, Csuka D.
    Genes (Basel); 2021 Mar 11; 12(3):. PubMed ID: 33799813
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  • 9. Definition and classification of hereditary angioedema.
    Proper SP, Lavery WJ, Bernstein JA.
    Allergy Asthma Proc; 2020 Nov 01; 41(Suppl 1):S03-S07. PubMed ID: 33109317
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  • 12. 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 01; 69(3):443-449. PubMed ID: 31959500
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  • 13. 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 15; 919():148496. PubMed ID: 38679185
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  • 16. In Search of an Association Between Genotype and Phenotype in Hereditary Angioedema due to C1-INH Deficiency.
    Loli-Ausejo D, López-Lera A, Drouet C, Lluncor M, Phillips-Anglés E, Pedrosa M, Cabañas R, Caballero T.
    Clin Rev Allergy Immunol; 2021 Aug 15; 61(1):1-14. PubMed ID: 33469833
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  • 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 15; 48(7):485-491. PubMed ID: 27187751
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