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Journal Abstract Search

473 related items for PubMed ID: 25249065

  • 21. Plasma biomarkers of acute attacks in patients with angioedema due to C1-inhibitor deficiency.
    Cugno M, Zanichelli A, Bellatorre AG, Griffini S, Cicardi M.
    Allergy; 2009 Feb; 64(2):254-7. PubMed ID: 19076541
    [Abstract] [Full Text] [Related]

  • 22. Hereditary angioedema in a family presenting as transient periarthritis.
    Adhikesavan LG, Olenginski TP.
    J Clin Rheumatol; 2008 Oct; 14(5):289-91. PubMed ID: 18824924
    [Abstract] [Full Text] [Related]

  • 23. Exploring disease-specific metabolite signatures in hereditary angioedema patients.
    Kanepa A, Fan J, Rots D, Vaska A, Ansone L, Briviba M, Klovins J, Kurjane N, Klavins K.
    Front Immunol; 2024 Oct; 15():1324671. PubMed ID: 38726011
    [Abstract] [Full Text] [Related]

  • 24. Hereditary angioedema: Historical aspects, classification, pathophysiology, clinical presentation, and laboratory diagnosis.
    Khan DA.
    Allergy Asthma Proc; 2011 Oct; 32(1):1-10. PubMed ID: 21262092
    [Abstract] [Full Text] [Related]

  • 25. 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 Oct; 36(3):206-12. PubMed ID: 25803135
    [Abstract] [Full Text] [Related]

  • 26. Diagnosis and treatment of bradykinin-mediated angioedema: outcomes from an angioedema expert consensus meeting.
    Craig TJ, Bernstein JA, Farkas H, Bouillet L, Boccon-Gibod I.
    Int Arch Allergy Immunol; 2014 Oct; 165(2):119-27. PubMed ID: 25401373
    [Abstract] [Full Text] [Related]

  • 27. 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
    [Abstract] [Full Text] [Related]

  • 28. An evaluation of tests used for the diagnosis and monitoring of C1 inhibitor deficiency: normal serum C4 does not exclude hereditary angio-oedema.
    Tarzi MD, Hickey A, Förster T, Mohammadi M, Longhurst HJ.
    Clin Exp Immunol; 2007 Sep; 149(3):513-6. PubMed ID: 17614974
    [Abstract] [Full Text] [Related]

  • 29. Hereditary angioedema: case report of a family.
    Yilmaz M, Kendirli SG, Altintaş D, Bingöl G.
    Turk J Pediatr; 2000 Sep; 42(3):230-3. PubMed ID: 11105624
    [Abstract] [Full Text] [Related]

  • 30. C1-inhibitor (C1-INH) autoantibodies in hereditary angioedema. Strong correlation with the severity of disease in C1-INH concentrate naïve patients.
    Varga L, Széplaki G, Visy B, Füst G, Harmat G, Miklós K, Németh J, Cervenak L, Karádi I, Farkas H.
    Mol Immunol; 2007 Feb; 44(6):1454-60. PubMed ID: 16750855
    [Abstract] [Full Text] [Related]

  • 31. Diagnosis and management of hereditary angioedema.
    Johnston DT.
    J Am Osteopath Assoc; 2011 Jan; 111(1):28-36. PubMed ID: 21258014
    [Abstract] [Full Text] [Related]

  • 32. Screening for hereditary angioedema (HAE) at 13 emergency centers in Osaka, Japan: A prospective observational study.
    Hirose T, Kimbara F, Shinozaki M, Mizushima Y, Yamamoto H, Kishi M, Kiguchi T, Shiono S, Noborio M, Fuke A, Akimoto H, Kimura T, Kaga S, Horiuchi T, Shimazu T.
    Medicine (Baltimore); 2017 Feb; 96(6):e6109. PubMed ID: 28178173
    [Abstract] [Full Text] [Related]

  • 33. Treatment of laryngeal hereditary angioedema.
    Richman MJ, Talan DA, Lumry WR.
    J Emerg Med; 2012 Jan; 42(1):44-7. PubMed ID: 21315535
    [Abstract] [Full Text] [Related]

  • 34. Chapter 22: Hereditary and acquired angioedema.
    Georgy MS, Pongracic JA.
    Allergy Asthma Proc; 2012 Jan; 33 Suppl 1():73-76. PubMed ID: 22794695
    [Abstract] [Full Text] [Related]

  • 35. 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
    [Abstract] [Full Text] [Related]

  • 36. Complement factor C4 activation in patients with hereditary angioedema.
    Aabom A, Bygum A, Koch C.
    Clin Biochem; 2017 Oct; 50(15):816-821. PubMed ID: 28412283
    [Abstract] [Full Text] [Related]

  • 37. Update on laboratory tests for the diagnosis and differentiation of hereditary angioedema and acquired angioedema.
    Frazer-Abel A, Giclas PC.
    Allergy Asthma Proc; 2011 Oct; 32 Suppl 1():17-21. PubMed ID: 22195757
    [Abstract] [Full Text] [Related]

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

  • 39. Type I and Type II Hereditary Angioedema: Clinical and Laboratory Findings in Iranian Patients.
    Kargarsharif F, Mehranmehr N, Zahedi Fard S, Fazlollahi MR, Ayazi M, Mohammadzadeh I, Nabavi M, Bemanian MH, Fayezi A, Movahedi M, Heidarzadeh M, Kalantari N, Arefimehr S, Saghafi S, Pourpak Z.
    Arch Iran Med; 2015 Jul; 18(7):425-9. PubMed ID: 26161706
    [Abstract] [Full Text] [Related]

  • 40. A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy.
    Zanichelli A, Arcoleo F, Barca MP, Borrelli P, Bova M, Cancian M, Cicardi M, Cillari E, De Carolis C, De Pasquale T, Del Corso I, Di Rocco PC, Guarino MD, Massaro I, Minale P, Montinaro V, Neri S, Perricone R, Pucci S, Quattrocchi P, Rossi O, Triggiani M, Zanierato G, Zoli A.
    Orphanet J Rare Dis; 2015 Feb 06; 10():11. PubMed ID: 25758562
    [Abstract] [Full Text] [Related]

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