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Journal Abstract Search

487 related items for PubMed ID: 33442779

  • 21. 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]

  • 22. 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; 61(1):60-65. PubMed ID: 33755867
    [Abstract] [Full Text] [Related]

  • 23. Angioedema Without Wheals: Challenges in Laboratorial Diagnosis.
    Grumach AS, Veronez CL, Csuka D, Farkas H.
    Front Immunol; 2021 Aug; 12():785736. PubMed ID: 34956216
    [Abstract] [Full Text] [Related]

  • 24. sgp120 and the contact system in hereditary angioedema: A diagnostic tool in HAE with normal C1 inhibitor.
    Larrauri B, Hester CG, Jiang H, Miletic VD, Malbran A, Bork K, Kaplan A, Frank M.
    Mol Immunol; 2020 Mar; 119():27-34. PubMed ID: 31955064
    [Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. 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 15; 6(4):1209-1216.e8. PubMed ID: 29128335
    [Abstract] [Full Text] [Related]

  • 27. Managing Diagnosis, Treatment, and Burden of Disease in Hereditary Angioedema Patients with Normal C1-Esterase Inhibitor.
    Jones D, Zafra H, Anderson J.
    J Asthma Allergy; 2023 Aug 15; 16():447-460. PubMed ID: 37124440
    [Abstract] [Full Text] [Related]

  • 28. 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 15; 44(12):1503-14. PubMed ID: 24552232
    [Abstract] [Full Text] [Related]

  • 29. Hereditary angioedema: Pathophysiology (HAE type I, HAE type II, and HAE nC1-INH).
    Wedner HJ.
    Allergy Asthma Proc; 2020 Nov 01; 41(Suppl 1):S14-S17. PubMed ID: 33109319
    [Abstract] [Full Text] [Related]

  • 30. A Missense Mutation of the Plasminogen Gene in a Japanese Family with Hereditary Angioedema with Normal C1 Inhibitor: Third Family Survey in Asia.
    Yakushiji H, Yamagami K, Hashimura C, Iwasaki H, Horiuchi T.
    Intern Med; 2023 Jul 01; 62(13):2005-2008. PubMed ID: 36418094
    [Abstract] [Full Text] [Related]

  • 31. Hereditary Angioedema with Normal C1 Inhibitor: Update on Evaluation and Treatment.
    Magerl M, Germenis AE, Maas C, Maurer M.
    Immunol Allergy Clin North Am; 2017 Aug 01; 37(3):571-584. PubMed ID: 28687110
    [Abstract] [Full Text] [Related]

  • 32. Deficiency of plasminogen activator inhibitor 2 in plasma of patients with hereditary angioedema with normal C1 inhibitor levels.
    Joseph K, Tholanikunnel BG, Wolf B, Bork K, Kaplan AP.
    J Allergy Clin Immunol; 2016 Jun 01; 137(6):1822-1829.e1. PubMed ID: 26395818
    [Abstract] [Full Text] [Related]

  • 33. 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]

  • 34. 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
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  • 38. The multifactorial impact of receiving a hereditary angioedema diagnosis.
    Raasch J, Glaum MC, O'Connor M.
    World Allergy Organ J; 2023 Jun 25; 16(6):100792. PubMed ID: 37448849
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