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Journal Abstract Search

311 related items for PubMed ID: 20804470

  • 1. 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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  • 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. Molecular diagnosis and management of hereditary angioedema in a Greek family.
    Papadopoulou-Alataki E, Foerster T, Antari V, Pavlitou-Tsiontsi A, Varlamis G.
    Int Arch Allergy Immunol; 2008 May; 147(2):166-70. PubMed ID: 18535392
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  • 5. A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family.
    Ferraro MF, Moreno AS, Castelli EC, Donadi EA, Palma MS, Arcuri HA, Lange AP, Bork K, Sarti W, Arruda LK.
    Allergy; 2011 Oct; 66(10):1384-90. PubMed ID: 21623829
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  • 9. 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; 70(11):925-9. PubMed ID: 19706314
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  • 10. Evidence of impaired sense of smell in hereditary angioedema.
    Perricone C, Agmon-Levin N, Shoenfeld N, de Carolis C, Guarino MD, Gigliucci G, Milana I, Novelli L, Valesini G, Perricone R, Shoenfeld Y.
    Allergy; 2011 Jan; 66(1):149-54. PubMed ID: 20649895
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  • 13. The Turkish Hereditary Angioedema Pilot Study (TURHAPS): the first Turkish series of hereditary angioedema.
    Kesim B, Uyguner ZO, Gelincik A, Mete Gökmen N, Sin AZ, Karakaya G, Erdenen F, Ardeniz O, Ozşeker F, Gülbahar O, Colakoğlu B, Dal M, Büyüköztürk S.
    Int Arch Allergy Immunol; 2011 Jan; 156(4):443-50. PubMed ID: 21832835
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  • 14. A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor.
    Bork K, Wulff K, Meinke P, Wagner N, Hardt J, Witzke G.
    Clin Immunol; 2011 Oct; 141(1):31-5. PubMed ID: 21849258
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  • 16. A new case of homozygous C1-inhibitor deficiency suggests a role for Arg378 in the control of kinin pathway activation.
    López-Lera A, Favier B, de la Cruz RM, Garrido S, Drouet C, López-Trascasa M.
    J Allergy Clin Immunol; 2010 Dec; 126(6):1307-10.e3. PubMed ID: 20864152
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  • 17. 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 Dec; 15(2):93-100. PubMed ID: 20306692
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  • 19. Mutational spectrum of the C1INH (SERPING1) gene in patients with hereditary angioedema.
    Gösswein T, Kocot A, Emmert G, Kreuz W, Martinez-Saguer I, Aygören-Pürsün E, Rusicke E, Bork K, Oldenburg J, Müller CR.
    Cytogenet Genome Res; 2008 Dec; 121(3-4):181-8. PubMed ID: 18758157
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  • 20. Mutation screening of the C1 inhibitor gene among Hungarian patients with hereditary angioedema.
    Kalmár L, Bors A, Farkas H, Vas S, Fandl B, Varga L, Füst G, Tordai A.
    Hum Mutat; 2003 Dec; 22(6):498. PubMed ID: 14635117
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