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954 related items for PubMed ID: 27271546

  • 1. Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema.
    Deroux A, Boccon-Gibod I, Fain O, Pralong P, Ollivier Y, Pagnier A, Djenouhat K, Du-Thanh A, Gompel A, Faisant C, Launay D, Bouillet L.
    Clin Exp Immunol; 2016 Sep; 185(3):332-7. PubMed ID: 27271546
    [Abstract] [Full Text] [Related]

  • 2. Hereditary angioedema with normal C1 inhibitor: clinical characteristics and treatment response with plasma-derived human C1 inhibitor concentrate (Berinert®) in a French cohort.
    Bouillet L, Boccon-Gibod I, Gompel A, Floccard B, Martin L, Blanchard-Delaunay C, Launay D, Fain O.
    Eur J Dermatol; 2017 Apr 01; 27(2):155-159. PubMed ID: 28251901
    [Abstract] [Full Text] [Related]

  • 3. Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations.
    Bork K, Wulff K, Witzke G, Hardt J.
    Allergy; 2015 Aug 01; 70(8):1004-12. PubMed ID: 25952149
    [Abstract] [Full Text] [Related]

  • 4. Coagulation Factor XII Gene Mutation in Brazilian Families with Hereditary Angioedema with Normal C1 Inhibitor.
    Moreno AS, Valle SO, Levy S, França AT, Serpa FS, Arcuri HA, Palma MS, Campos WN, Dias MM, Ponard D, Monnier N, Lunardi J, Bork K, Silva WA, Arruda LK.
    Int Arch Allergy Immunol; 2015 Aug 01; 166(2):114-20. PubMed ID: 25790805
    [Abstract] [Full Text] [Related]

  • 5. 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 Aug 01; 6(4):1209-1216.e8. PubMed ID: 29128335
    [Abstract] [Full Text] [Related]

  • 6. 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 01; 72(2):320-324. PubMed ID: 27905115
    [Abstract] [Full Text] [Related]

  • 7. Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence.
    Bork K, Machnig T, Wulff K, Witzke G, Prusty S, Hardt J.
    Orphanet J Rare Dis; 2020 Oct 15; 15(1):289. PubMed ID: 33059692
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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 15; 157(2):239-48. PubMed ID: 25744496
    [Abstract] [Full Text] [Related]

  • 10. Impaired control of the contact system in hereditary angioedema with normal C1-inhibitor.
    Bova M, Suffritti C, Bafunno V, Loffredo S, Cordisco G, Del Giacco S, De Pasquale TMA, Firinu D, Margaglione M, Montinaro V, Petraroli A, Radice A, Brussino L, Zanichelli A, Zoli A, Cicardi M.
    Allergy; 2020 Jun 15; 75(6):1394-1403. PubMed ID: 31860755
    [Abstract] [Full Text] [Related]

  • 11. Hereditary angioedema with normal C1 inhibitor in a French cohort: Clinical characteristics and response to treatment with icatibant.
    Bouillet L, Boccon-Gibod I, Launay D, Gompel A, Kanny G, Fabien V, Fain O, IOS Study Group.
    Immun Inflamm Dis; 2017 Mar 15; 5(1):29-36. PubMed ID: 28250922
    [Abstract] [Full Text] [Related]

  • 12. Hereditary angioedema with normal C1-inhibitor: Clinical and genetic characterization of 15 Portuguese unrelated families.
    Dias de Castro E, Pinhal AL, Bragança M, Parente Freixo J, Martinho A.
    Ann Allergy Asthma Immunol; 2024 Jun 15; 132(6):730-736. PubMed ID: 38342132
    [Abstract] [Full Text] [Related]

  • 13. Hereditary and acquired C1-inhibitor-dependent angioedema: from pathophysiology to treatment.
    Zeerleder S, Levi M.
    Ann Med; 2016 Jun 15; 48(4):256-67. PubMed ID: 27018196
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  • 15. Unnecessary Abdominal Surgeries in Attacks of Hereditary Angioedema with Normal C1 Inhibitor.
    Gutierrez M, Veronez CL, Rodrigues Valle SO, Gonçalves RF, Ferriani MPL, Moreno AS, Arruda LK, Aun MV, Giavina-Bianchi P, Alonso MLO, Pesquero JB, Grumach AS.
    Clin Rev Allergy Immunol; 2021 Aug 15; 61(1):60-65. PubMed ID: 33755867
    [Abstract] [Full Text] [Related]

  • 16. Plasmin is a natural trigger for bradykinin production in patients with hereditary angioedema with factor XII mutations.
    de Maat S, Björkqvist J, Suffritti C, Wiesenekker CP, Nagtegaal W, Koekman A, van Dooremalen S, Pasterkamp G, de Groot PG, Cicardi M, Renné T, Maas C.
    J Allergy Clin Immunol; 2016 Nov 15; 138(5):1414-1423.e9. PubMed ID: 27130860
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