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195 related items for PubMed ID: 26248961

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  • 23. Analysis of SERPING1 expression on hereditary angioedema patients: quantitative analysis of full-length and exon 3 splicing variants.
    de la Cruz RM, López-Lera A, López-Trascasa M.
    Immunol Lett; 2012 Jan 30; 141(2):158-64. PubMed ID: 22001489
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  • 24. Novel duplication in the F12 gene in a patient with recurrent angioedema.
    Kiss N, Barabás E, Várnai K, Halász A, Varga LÁ, Prohászka Z, Farkas H, Szilágyi Á.
    Clin Immunol; 2013 Oct 30; 149(1):142-5. PubMed ID: 23994767
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  • 25. 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 30; 61(1):1-14. PubMed ID: 33469833
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  • 26. Association after linkage analysis indicates that homozygosity for the 46C-->T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis.
    Tirado I, Soria JM, Mateo J, Oliver A, Souto JC, Santamaria A, Felices R, Borrell M, Fontcuberta J.
    Thromb Haemost; 2004 May 30; 91(5):899-904. PubMed ID: 15116249
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  • 27. Hereditary angioedema nationwide study in Slovenia reveals four novel mutations in SERPING1 gene.
    Rijavec M, Korošec P, Šilar M, Zidarn M, Miljković J, Košnik M.
    PLoS One; 2013 May 30; 8(2):e56712. PubMed ID: 23437219
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  • 35. An investigational RNAi therapeutic targeting Factor XII (ALN-F12) for the treatment of hereditary angioedema.
    Liu J, Qin J, Borodovsky A, Racie T, Castoreno A, Schlegel M, Maier MA, Zimmerman T, Fitzgerald K, Butler J, Akinc A.
    RNA; 2019 Feb 30; 25(2):255-263. PubMed ID: 30463937
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  • 36. Paternal mosaicism and hereditary angioedema in a Taiwanese family.
    Yu TC, Shyur SD, Huang LH, Wen DC, Li JS.
    Ann Allergy Asthma Immunol; 2007 Oct 30; 99(4):375-9. PubMed ID: 17941288
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  • 37. [Hereditary angioedema biological diagnosis].
    Ponard D.
    Presse Med; 2015 Jan 30; 44(1):57-64. PubMed ID: 25511654
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  • 38. Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE).
    Parsopoulou F, Loules G, Zamanakou M, Csuka D, Szilagyi A, Kompoti M, Porebski G, Psarros F, Magerl M, Valerieva A, Staevska M, Obtulowicz K, Maurer M, Speletas M, Farkas H, Germenis AE.
    Front Allergy; 2022 Jan 30; 3():868185. PubMed ID: 35873600
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