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Journal Abstract Search

159 related items for PubMed ID: 23123409

  • 21. Molecular genetics of C1 inhibitor.
    Tosi M.
    Immunobiology; 1998 Aug; 199(2):358-65. PubMed ID: 9777419
    [Abstract] [Full Text] [Related]

  • 22. Deletions in SERPING1 Lead to Lower C1 Inhibitor Function: Lower C1 Inhibitor Function Can Predict Disease Severity.
    Mete Gökmen N, Gülbahar O, Onay H, Peker Koc Z, Özgül S, Köse T, Gelincik A, Büyüköztürk S, Sin AZ.
    Int Arch Allergy Immunol; 2019 Aug; 178(1):50-59. PubMed ID: 30278448
    [Abstract] [Full Text] [Related]

  • 23. Genetics of Hereditary Angioedema Revisited.
    Germenis AE, Speletas M.
    Clin Rev Allergy Immunol; 2016 Oct; 51(2):170-82. PubMed ID: 27116602
    [Abstract] [Full Text] [Related]

  • 24. SERPING1 mutations in 59 families with hereditary angioedema.
    López-Lera A, Garrido S, Roche O, López-Trascasa M.
    Mol Immunol; 2011 Oct; 49(1-2):18-27. PubMed ID: 21864911
    [Abstract] [Full Text] [Related]

  • 25. Identification and characterization of a novel splice site mutation in the SERPING1 gene in a family with hereditary angioedema.
    Colobran R, Lois S, de la Cruz X, Pujol-Borrell R, Hernández-González M, Guilarte M.
    Clin Immunol; 2014 Feb; 150(2):143-8. PubMed ID: 24412907
    [Abstract] [Full Text] [Related]

  • 26. New mutations in C1 esterase inhibitor (SERPING1) in a German family with hereditary angioedema.
    El-Meguid AM, Aslanidis C, Schimanski S, Schambeck C, Schmitz G.
    Egypt J Immunol; 2008 Feb; 15(2):93-100. PubMed ID: 20306692
    [Abstract] [Full Text] [Related]

  • 27. Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency.
    Loules G, Zamanakou M, Parsopoulou F, Vatsiou S, Psarros F, Csuka D, Porebski G, Obtulowicz K, Valerieva A, Staevska M, López-Lera A, López-Trascasa M, Moldovan D, Magerl M, Maurer M, Speletas M, Farkas H, Germenis AE.
    Gene; 2018 Aug 15; 667():76-82. PubMed ID: 29753808
    [Abstract] [Full Text] [Related]

  • 28. Presence of C1-inhibitor polymers in a subset of patients suffering from hereditary angioedema.
    Madsen DE, Hansen S, Gram J, Bygum A, Drouet C, Sidelmann JJ.
    PLoS One; 2014 Aug 15; 9(11):e112051. PubMed ID: 25369003
    [Abstract] [Full Text] [Related]

  • 29. 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 25; 498(1):193-198. PubMed ID: 29548426
    [Abstract] [Full Text] [Related]

  • 30. Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema.
    Szabó E, Csuka D, Andrási N, Varga L, Farkas H, Szilágyi Á.
    Front Allergy; 2022 Mar 25; 3():836465. PubMed ID: 35386643
    [Abstract] [Full Text] [Related]

  • 31. Normal C1 inhibitor mRNA expression level in type I hereditary angioedema patients: newly found C1 inhibitor gene mutations.
    Kang HR, Yim EY, Oh SY, Chang YS, Kim YK, Cho SH, Min KU, Kim YY.
    Allergy; 2006 Feb 25; 61(2):260-4. PubMed ID: 16409206
    [Abstract] [Full Text] [Related]

  • 32. 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 25; 18(3):215-223. PubMed ID: 32065705
    [Abstract] [Full Text] [Related]

  • 33. Hereditary angioedema in Greek families caused by novel and recurrent mutations.
    Speletas M, Boukas K, Papadopoulou-Alataki E, Tsitsami E, Germenis AE.
    Hum Immunol; 2009 Nov 25; 70(11):925-9. PubMed ID: 19706314
    [Abstract] [Full Text] [Related]

  • 34. Detection of C1 inhibitor mutations in patients with hereditary angioedema.
    Zuraw BL, Herschbach J.
    J Allergy Clin Immunol; 2000 Mar 25; 105(3):541-6. PubMed ID: 10719305
    [Abstract] [Full Text] [Related]

  • 35. Hereditary angioedema: a Taiwanese family with a novel gene mutation.
    Wen DC, Shyur SD, Wu JY, Lin CC, Chiang YC, Huang LH, Lin MT, Yang HC, Liang PH.
    Asian Pac J Allergy Immunol; 2007 Mar 25; 25(2-3):163-7. PubMed ID: 18035804
    [Abstract] [Full Text] [Related]

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  • 37. Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations.
    Blanch A, Roche O, López-Granados E, Fontán G, López-Trascasa M.
    Hum Mutat; 2002 Nov 25; 20(5):405-6. PubMed ID: 12402344
    [Abstract] [Full Text] [Related]

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  • 39. Hereditary angioedema in Japan: genetic analysis of 13 unrelated cases.
    Yamamoto T, Horiuchi T, Miyahara H, Yoshizawa S, Maehara J, Shono E, Takamura K, Machida H, Tsujioka K, Kaneko T, Uemura N, Suzawa K, Inagaki N, Umegaki N, Kasamatsu Y, Hara A, Arinobu Y, Inoue Y, Niiro H, Kashiwagai Y, Harashima S, Tahira T, Tsukamoto H, Akashi K.
    Am J Med Sci; 2012 Mar 25; 343(3):210-4. PubMed ID: 21934598
    [Abstract] [Full Text] [Related]

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