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Journal Abstract Search

250 related items for PubMed ID: 30118244

  • 1. A hereditary angioedema screening on an index case: Turkey.
    Ozkars MY, Keskin O, Bayram N, Keskin M, Bayram H, Sahin Y, Kucukosmanoglu E, Attila N, Kirik SK.
    Asian Pac J Allergy Immunol; 2019 Sep; 37(3):154-161. PubMed ID: 30118244
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  • 2. Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel SERPING1 mutations and genetic factors modifying the clinical phenotype.
    Grivčeva-Panovska V, Košnik M, Korošec P, Andrejević S, Karadža-Lapić L, Rijavec M.
    Ann Med; 2018 May; 50(3):269-276. PubMed ID: 29513108
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  • 3. High-molecular-weight kininogen cleavage correlates with disease states in the bradykinin-mediated angioedema due to hereditary C1-inhibitor deficiency.
    Suffritti C, Zanichelli A, Maggioni L, Bonanni E, Cugno M, Cicardi M.
    Clin Exp Allergy; 2014 Dec; 44(12):1503-14. PubMed ID: 24552232
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  • 6. 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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  • 7. 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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  • 9. A hereditary angioedema screening in two villages, based on an index case, and identification of a novel mutation, "1033G>T", at the SERPING1 gene.
    Ozkars MY, Keskın O, Bayram N, Onay H, Keskın M, Bayram H, Sahın Y, Küçükosmanoğlu E, Kırık S.
    Postepy Dermatol Alergol; 2019 Aug 15; 36(4):403-411. PubMed ID: 31616213
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  • 10. 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 15; 178(1):50-59. PubMed ID: 30278448
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  • 12. Presentation, diagnosis and treatment of angioedema without wheals: a retrospective analysis of a cohort of 1058 patients.
    Mansi M, Zanichelli A, Coerezza A, Suffritti C, Wu MA, Vacchini R, Stieber C, Cichon S, Cicardi M.
    J Intern Med; 2015 May 15; 277(5):585-93. PubMed ID: 25196353
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  • 13. Idiopathic Nonhistaminergic Acquired Angioedema Versus Hereditary Angioedema.
    Andrási N, Veszeli N, Kőhalmi KV, Csuka D, Temesszentandrási G, Varga L, Farkas H.
    J Allergy Clin Immunol Pract; 2018 May 15; 6(4):1205-1208. PubMed ID: 29715562
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  • 15. 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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  • 16. 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 15; 18(3):215-223. PubMed ID: 32065705
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  • 18. Diagnosis and treatment of hereditary angioedema.
    Canonica GW, Rossi O.
    Panminerva Med; 2012 Sep 15; 54(3):241-53. PubMed ID: 22801442
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