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Journal Abstract Search

226 related items for PubMed ID: 14572811

  • 1. Management of hereditary angioedema: a Canadian approach.
    Bowen T, Hebert J, Ritchie B, Burnham J, MacSween M, Warrington R, Yang W, Issekutz A, Karitsiotis N, McCombie N, Giulivi T.
    Transfus Apher Sci; 2003 Dec; 29(3):205-14. PubMed ID: 14572811
    [Abstract] [Full Text] [Related]

  • 2. Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary Angioedema.
    Bowen T, Cicardi M, Farkas H, Bork K, Kreuz W, Zingale L, Varga L, Martinez-Saguer I, Aygören-Pürsün E, Binkley K, Zuraw B, Davis A, Hebert J, Ritchie B, Burnham J, Castaldo A, Menendez A, Nagy I, Harmat G, Bucher C, Lacuesta G, Issekutz A, Warrington R, Yang W, Dean J, Kanani A, Stark D, McCusker C, Wagner E, Rivard GE, Leith E, Tsai E, MacSween M, Lyanga J, Serushago B, Leznoff A, Waserman S, de Serres J.
    J Allergy Clin Immunol; 2004 Sep; 114(3):629-37. PubMed ID: 15356569
    [Abstract] [Full Text] [Related]

  • 3. C1-esterase inhibitor transfusions in patients with hereditary angioedema.
    Visentin DE, Yang WH, Karsh J.
    Ann Allergy Asthma Immunol; 1998 Jun; 80(6):457-61. PubMed ID: 9647267
    [Abstract] [Full Text] [Related]

  • 4. Effective treatment of hereditary angioedema with fresh frozen plasma in an emergency department.
    Pekdemir M, Ersel M, Aksay E, Yanturali S, Akturk A, Kiyan S.
    J Emerg Med; 2007 Aug; 33(2):137-9. PubMed ID: 17692764
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. A new type of acquired C1 inhibitor deficiency associated with systemic lupus erythematosus.
    Cacoub P, Frémeaux-Bacchi V, De Lacroix I, Guillien F, Kahn MF, Kazatchkine MD, Godeau P, Piette JC.
    Arthritis Rheum; 2001 Aug 30; 44(8):1836-40. PubMed ID: 11508436
    [Abstract] [Full Text] [Related]

  • 7. [Hereditary or acquired angioedema caused by functional deficiency of C1 inhibitor--a still unfamiliar disease picture].
    Wüthrich B, Devay J, Späth P.
    Schweiz Med Wochenschr; 1999 Feb 20; 129(7):285-91. PubMed ID: 10093876
    [Abstract] [Full Text] [Related]

  • 8. International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency.
    Caballero T, Farkas H, Bouillet L, Bowen T, Gompel A, Fagerberg C, Bjökander J, Bork K, Bygum A, Cicardi M, de Carolis C, Frank M, Gooi JH, Longhurst H, Martínez-Saguer I, Nielsen EW, Obtulowitz K, Perricone R, Prior N, C-1-INH Deficiency Working Group.
    J Allergy Clin Immunol; 2012 Feb 20; 129(2):308-20. PubMed ID: 22197274
    [Abstract] [Full Text] [Related]

  • 9. Management of hereditary angioedema: 2010 Canadian approach.
    Bowen T, Brosz J, Brosz K, Hebert J, Ritchie B.
    Allergy Asthma Clin Immunol; 2010 Jul 28; 6(1):20. PubMed ID: 20667123
    [Abstract] [Full Text] [Related]

  • 10. Diagnosis and management of hereditary angioedema: an American approach.
    Zuraw BL.
    Transfus Apher Sci; 2003 Dec 28; 29(3):239-45. PubMed ID: 14572816
    [Abstract] [Full Text] [Related]

  • 11.
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    [No Abstract] [Full Text] [Related]

  • 12. The Hungarian HAE experience.
    Farkas H, Varga L.
    Transfus Apher Sci; 2003 Dec 28; 29(3):229-33. PubMed ID: 14572814
    [Abstract] [Full Text] [Related]

  • 13. C1-inhibitor deficiency (hereditary angioedema): case report and review.
    Burge JJ.
    Va Med; 1983 Dec 28; 110(12):706-11. PubMed ID: 6364593
    [No Abstract] [Full Text] [Related]

  • 14. [Hereditary angioedema in a 16-year-old girl].
    Kozowicz M, Kordys-Darmolińska B, Kasznia-Kocot J, Woś H, Zukowska B, Kwaśniak A.
    Wiad Lek; 2006 Dec 28; 59(11-12):869-72. PubMed ID: 17427507
    [Abstract] [Full Text] [Related]

  • 15. How do we treat patients with hereditary angioedema.
    Cicardi M, Zingale L.
    Transfus Apher Sci; 2003 Dec 28; 29(3):221-7. PubMed ID: 14572813
    [Abstract] [Full Text] [Related]

  • 16. [Deficiencies of C1 inhibitor: hereditary and acquired angioedema].
    Porcel-Pérez JM, López-Trascasa M.
    Rev Clin Esp; 1996 Mar 28; 196 Spec No():26-30. PubMed ID: 9206804
    [No Abstract] [Full Text] [Related]

  • 17. C1 inhibitor deficiency: diagnosis.
    Gompels MM, Lock RJ.
    Clin Exp Dermatol; 2005 Jul 28; 30(4):460-2. PubMed ID: 15953110
    [Abstract] [Full Text] [Related]

  • 18. Management of hereditary angioedema in pediatric patients.
    Farkas H, Varga L, Széplaki G, Visy B, Harmat G, Bowen T.
    Pediatrics; 2007 Sep 28; 120(3):e713-22. PubMed ID: 17724112
    [Abstract] [Full Text] [Related]

  • 19. [Hereditary angioneurotic edema: a molecular disease caused by a defect in the O-glycosylation of C1 esterase inhibitor (C1-INH)].
    Ollier-Hartmann MP, Strecker G, Montreuil J, Hartmann L.
    C R Acad Sci III; 1984 Sep 28; 299(16):667-9. PubMed ID: 6440668
    [Abstract] [Full Text] [Related]

  • 20. Hereditary angioedema due to deficit of C1 esterase inhibitor.
    Zeana C.
    Med Interne; 1989 Sep 28; 27(2):143-7. PubMed ID: 2814292
    [Abstract] [Full Text] [Related]

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