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Journal Abstract Search

431 related items for PubMed ID: 25609336

  • 1. Comparison of chromogenic and ELISA functional C1 inhibitor tests in diagnosing hereditary angioedema.
    Li HH, Busse P, Lumry WR, Frazer-Abel A, Levy H, Steele T, Dayno J, Riedl M.
    J Allergy Clin Immunol Pract; 2015; 3(2):200-5. PubMed ID: 25609336
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  • 2. Diagnosis and treatment of hereditary angioedema.
    Canonica GW, Rossi O.
    Panminerva Med; 2012 Sep; 54(3):241-53. PubMed ID: 22801442
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  • 5. A first of its kind quantitative functional C1-esterase inhibitor lateral flow assay for hereditary angioedema point-of-care diagnostic testing.
    Chockalingam PS, Zhou Z, Garg BK, Boehringer H, Chung R, Fait S.
    Int Immunopharmacol; 2020 Jun; 83():106526. PubMed ID: 32361670
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  • 7. Prevalence of hereditary angioedema in untested first-degree blood relatives of known subjects with hereditary angioedema.
    Riedl MA, Lumry WR, Busse P, Levy H, Steele T, Dayno J, Li HH.
    Allergy Asthma Proc; 2015 Jun; 36(3):206-12. PubMed ID: 25803135
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  • 8. Is there a need for clinical guidelines in the United States for the diagnosis of hereditary angioedema and the screening of family members of affected patients?
    Lunn ML, Santos CB, Craig TJ.
    Ann Allergy Asthma Immunol; 2010 Mar; 104(3):211-4. PubMed ID: 20377110
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  • 10. Shortened Activated Partial Thromboplastin Time May Help in Diagnosing Hereditary and Acquired Angioedema.
    Bork K, Witzke G.
    Int Arch Allergy Immunol; 2016 Mar; 170(2):101-7. PubMed ID: 27463190
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  • 11. HEREDITARY ANGIOEDEMA DUE TO C1-INHIBITOR DEFICIENCY IN PEDIATRIC PATIENTS IN CROATIA - FIRST NATIONAL STUDY, DIAGNOSTIC AND PROPHYLACTIC CHALLENGES.
    Karadža-Lapić L, Barešić M, Vrsalović R, Ivković-Jureković I, Sršen S, Prkačin I, Rijavec M, Cikojević D.
    Acta Clin Croat; 2019 Mar; 58(1):139-146. PubMed ID: 31363336
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  • 12. Angioedema Without Wheals: Challenges in Laboratorial Diagnosis.
    Grumach AS, Veronez CL, Csuka D, Farkas H.
    Front Immunol; 2021 Mar; 12():785736. PubMed ID: 34956216
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  • 13. 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
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  • 14. 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 Sep; 6(4):1205-1208. PubMed ID: 29715562
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  • 15. Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations.
    Wagenaar-Bos IG, Drouet C, Aygören-Pursun E, Bork K, Bucher C, Bygum A, Farkas H, Fust G, Gregorek H, Hack CE, Hickey A, Joller-Jemelka HI, Kapusta M, Kreuz W, Longhurst H, Lopez-Trascasa M, Madalinski K, Naskalski J, Nieuwenhuys E, Ponard D, Truedsson L, Varga L, Nielsen EW, Wagner E, Zingale L, Cicardi M, van Ham SM.
    J Immunol Methods; 2008 Sep 30; 338(1-2):14-20. PubMed ID: 18655790
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  • 16. Complement factor C4 activation in patients with hereditary angioedema.
    Aabom A, Bygum A, Koch C.
    Clin Biochem; 2017 Oct 30; 50(15):816-821. PubMed ID: 28412283
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  • 17. Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency.
    Zanichelli A, Azin GM, Wu MA, Suffritti C, Maggioni L, Caccia S, Perego F, Vacchini R, Cicardi M.
    J Allergy Clin Immunol Pract; 2017 Oct 30; 5(5):1307-1313. PubMed ID: 28284781
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  • 19. 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 Oct 30; 6(4):1209-1216.e8. PubMed ID: 29128335
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