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Journal Abstract Search

715 related items for PubMed ID: 29513108

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  • 3. Genetic Determinants of C1 Inhibitor Deficiency Angioedema Age of Onset.
    Gianni P, Loules G, Zamanakou M, Kompoti M, Csuka D, Psarros F, Magerl M, Moldovan D, Maurer M, Speletas MG, Farkas H, Germenis AE.
    Int Arch Allergy Immunol; 2017; 174(3-4):200-204. PubMed ID: 29130992
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  • 4. 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
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  • 6. 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; 61(1):1-14. PubMed ID: 33469833
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  • 7. 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
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  • 8. F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.
    Speletas M, Szilágyi Á, Csuka D, Koutsostathis N, Psarros F, Moldovan D, Magerl M, Kompoti M, Varga L, Maurer M, Farkas H, Germenis AE.
    Allergy; 2015 Dec; 70(12):1661-4. PubMed ID: 26248961
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  • 12. 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 Dec; 6(4):1209-1216.e8. PubMed ID: 29128335
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  • 14. 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
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  • 17. Mutational spectrum and phenotypes in Danish families with hereditary angioedema because of C1 inhibitor deficiency.
    Bygum A, Fagerberg CR, Ponard D, Monnier N, Lunardi J, Drouet C.
    Allergy; 2011 Jan; 66(1):76-84. PubMed ID: 20804470
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  • 18. Genetics of Hereditary Angioedema Revisited.
    Germenis AE, Speletas M.
    Clin Rev Allergy Immunol; 2016 Oct; 51(2):170-82. PubMed ID: 27116602
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  • 19. 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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  • 20. 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 01; 60(3):305-315. PubMed ID: 33442779
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