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Journal Abstract Search

195 related items for PubMed ID: 26248961

  • 1. 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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  • 2. 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 Dec; 174(3-4):200-204. PubMed ID: 29130992
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  • 6. Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association.
    Andrejević S, Korošec P, Šilar M, Košnik M, Mijanović R, Bonači-Nikolić B, Rijavec M.
    PLoS One; 2015 Dec; 10(11):e0142174. PubMed ID: 26535898
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  • 7. 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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  • 8. Characterization of patients with angioedema without wheals: the importance of F12 gene screening.
    Firinu D, Bafunno V, Vecchione G, Barca MP, Manconi PE, Santacroce R, Margaglione M, Del Giacco SR.
    Clin Immunol; 2015 Apr; 157(2):239-48. PubMed ID: 25744496
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  • 9. 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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  • 12. Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
    Charignon D, Ghannam A, Defendi F, Ponard D, Monnier N, López Trascasa M, Launay D, Caballero T, Djenouhat K, Fain O, Cichon S, Martin L, Drouet C.
    Allergy; 2014 Dec; 69(12):1659-65. PubMed ID: 25134986
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  • 13. Treatment for hereditary angioedema with normal C1-INH and specific mutations in the F12 gene (HAE-FXII).
    Bork K, Wulff K, Witzke G, Hardt J.
    Allergy; 2017 Feb; 72(2):320-324. PubMed ID: 27905115
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  • 16. 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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  • 19. Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations.
    Bafunno V, Bova M, Loffredo S, Divella C, Petraroli A, Marone G, Montinaro V, Margaglione M, Triggiani M.
    Ann Hum Genet; 2014 Mar 15; 78(2):73-82. PubMed ID: 24456027
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  • 20. Mutational spectrum of the SERPING1 gene in Swiss patients with hereditary angioedema.
    Steiner UC, Keller M, Schmid P, Cichon S, Wuillemin WA.
    Clin Exp Immunol; 2017 Jun 15; 188(3):430-436. PubMed ID: 28194776
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