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Journal Abstract Search

203 related items for PubMed ID: 36418094

  • 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. The Expanding Spectrum of Mutations in Hereditary Angioedema.
    Veronez CL, Csuka D, Sheikh FR, Zuraw BL, Farkas H, Bork K.
    J Allergy Clin Immunol Pract; 2021 Jun; 9(6):2229-2234. PubMed ID: 33746090
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  • 23. 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
    [Abstract] [Full Text] [Related]

  • 24. Identification of the recently described plasminogen gene mutation p.Lys330Glu in a family from Northern Germany with hereditary angioedema.
    Recke A, Massalme EG, Jappe U, Steinmüller-Magin L, Schmidt J, Hellenbroich Y, Hüning I, Gillessen-Kaesbach G, Zillikens D, Hartmann K.
    Clin Transl Allergy; 2019 May; 9():9. PubMed ID: 30809376
    [Abstract] [Full Text] [Related]

  • 25. Study of angiopoietin and plasminogen genes in hereditary angioedema.
    Kruk T, Chong-Neto HJ, Dias MM, Campos WN, Moreno AS, Mikami LR, Ferrari LP, Arruda LKP, Rosário Filho N.
    Rev Assoc Med Bras (1992); 2020 Apr; 66(4):502-506. PubMed ID: 32578786
    [Abstract] [Full Text] [Related]

  • 26. A clinical evaluation of patients with known mutations (plasminogen and factor XII) with a focus on prophylactic treatment.
    Lochbaum R, Trainotti S, Hoffmann TK, Greve J, Hahn J.
    J Dermatolog Treat; 2024 Dec; 35(1):2290362. PubMed ID: 38086754
    [Abstract] [Full Text] [Related]

  • 27. 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; 75(6):1394-1403. PubMed ID: 31860755
    [Abstract] [Full Text] [Related]

  • 28. 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; 132(6):730-736. PubMed ID: 38342132
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  • 30. Genetics of Hereditary Angioedema Revisited.
    Germenis AE, Speletas M.
    Clin Rev Allergy Immunol; 2016 Oct; 51(2):170-82. PubMed ID: 27116602
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  • 34. 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]

  • 35. 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
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  • 36. [Advances in the Pathogenesis of Hereditary Angioedema].
    Cao Y, Liu S, Zhi Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2020 Oct; 42(5):686-690. PubMed ID: 33131525
    [Abstract] [Full Text] [Related]

  • 37. Hereditary and acquired angioedema.
    Patel G, Pongracic JA.
    Allergy Asthma Proc; 2019 Nov 01; 40(6):441-445. PubMed ID: 31690390
    [Abstract] [Full Text] [Related]

  • 38. Efficacy, pharmacokinetics, and safety of subcutaneous C1-esterase inhibitor as prophylaxis in Japanese patients with hereditary angioedema: Results of a Phase 3 study.
    Fukuda T, Yamagami K, Kawahata K, Suzuki Y, Sasaki Y, Miyagi T, Jacobs I, Lawo JP, Glassman F, Akama H, Hide M, Ohsawa I.
    Allergol Int; 2023 Jul 01; 72(3):451-457. PubMed ID: 36858856
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  • 39. 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 Jul 01; 147(2):166-70. PubMed ID: 18535392
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