Diagnostik und Ausschluss des hereditären Angioödems
暂无分享,去创建一个
M. Maurer | R. Treudler | M. Ziemer | V. Wahn | M. Magerl | J. Brasch | U. Förster | B. Hauswald | B. Mohr | J. Präßler | R. Vetter | V. Zampelli
[1] M. Maurer,et al. Hereditäres Angioödem: Update zu verfügbaren Therapieoptionen , 2010 .
[2] L. Bielory,et al. Acquired angioedema: Autoantibody associations and C1q utility as a diagnostic tool. , 2010, Allergy and asthma proceedings.
[3] William H. Yang,et al. Icatibant, a new bradykinin-receptor antagonist, in hereditary angioedema. , 2010, The New England journal of medicine.
[4] J. Bernstein,et al. Nanofiltered C1 inhibitor concentrate for treatment of hereditary angioedema. , 2010, The New England journal of medicine.
[5] A. Sheffer,et al. Ecallantide for the treatment of acute attacks in hereditary angioedema. , 2010, The New England journal of medicine.
[6] P. Pundir,et al. Comparison of the inhibitory effects of resveratrol and tranilast on IgE, 48/80 and substance P dependent-mast cell activation , 2010, Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology.
[7] T. Craig,et al. Summary of the International Multicenter Prospective Angioedema C1-inhibitor Trials 1 and 2 (IMPACT1 and 2) , 2010, Expert review of clinical immunology.
[8] M. Maurer,et al. Erfolgreiche Behandlung des hereditären Angioödems mit dem Bradykinin‐B2‐Rezeptor‐Antagonisten Icatibant , 2010 .
[9] Diego S. Fernández Romero,et al. Angioedema hereditario: Historia familiar y manifestaciones clínicas en 58 pacientes , 2009 .
[10] A. Bygum,et al. Hereditary angio‐oedema in Denmark: a nationwide survey , 2009, The British journal of dermatology.
[11] T. Zuberbier,et al. Successful treatment of hereditary angioedema with bradykinin B2‐receptor antagonist icatibant , 2009, Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG.
[12] T. Craig,et al. Frequency, timing, and type of prodromal symptoms associated with hereditary angioedema attacks. , 2009, Allergy and asthma proceedings.
[13] T. Arita,et al. Computed tomography of the gastrointestinal manifestation of hereditary angioedema , 2008, Radiation Medicine.
[14] D. N. Patel,et al. Hereditary angioedema with normal C1 inhibitor. , 2008, The American journal of medicine.
[15] Pedro Mejia,et al. Biological activities of C1 inhibitor. , 2008, Molecular immunology.
[16] H. Joller-jemelka,et al. Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations. , 2008, Journal of immunological methods.
[17] M. Frank. 8. Hereditary angioedema. , 2008, The Journal of allergy and clinical immunology.
[18] G. Kojda,et al. Nonallergic angioedema: role of bradykinin , 2007, Allergy.
[19] M. Mohammadi,et al. An evaluation of tests used for the diagnosis and monitoring of C1 inhibitor deficiency: normal serum C4 does not exclude hereditary angio‐oedema , 2007, Clinical and experimental immunology.
[20] P. Schlattmann,et al. Treatment of acute edema attacks in hereditary angioedema with a bradykinin receptor-2 antagonist (Icatibant). , 2007, The Journal of allergy and clinical immunology.
[21] H. Farkas,et al. Recombinant human C1‐inhibitor in the treatment of acute angioedema attacks , 2007, Transfusion.
[22] S. Cichon,et al. Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III. , 2006, American journal of human genetics.
[23] M. Cicardi,et al. Angioedema without urticaria: a large clinical survey , 2006, Canadian Medical Association Journal.
[24] A. Eckardt,et al. Symptoms, Course, and Complications of Abdominal Attacks in Hereditary Angioedema Due to C1 Inhibitor Deficiency , 2006, The American Journal of Gastroenterology.
[25] K. Bork,et al. Hereditary angioedema: new findings concerning symptoms, affected organs, and course. , 2006, The American journal of medicine.
[26] M. Tang,et al. Hereditary angio‐oedema in children: A management guideline , 2005, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.
[27] M. López-Trascasa,et al. Hereditary angioedema due to C1 inhibitor deficiency: patient registry and approach to the prevalence in Spain. , 2005, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.
[28] M. Gompels,et al. C1 inhibitor deficiency: consensus document , 2005, Clinical and experimental immunology.
[29] A. Tordai,et al. Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond , 2004, Journal of Allergy and Clinical Immunology.
[30] M. Cicardi,et al. C1 inhibitor concentrate therapy in 473 patients with hereditary and acquired angioedema , 2004 .
[31] H. Griffiths,et al. Normal complement C4 values do not exclude hereditary angioedema , 2004, Journal of Clinical Pathology.
[32] K. Dirks,et al. Sonographie beim hereditären Angioödem: Typische Befunde anhand dreier Kasuistiken , 2001 .
[33] K. Bork,et al. Hereditary angioedema with normal C1-inhibitor activity in women , 2000, The Lancet.
[34] M. Cicardi,et al. Plasma bradykinin in angio-oedema , 1998, The Lancet.
[35] H. Hintner,et al. Untersuchungen zum hereditären Angioödem im deutschsprachigen Raum , 1998, Der Hautarzt.
[36] A. Malbrán,et al. [Hereditary angioedema. Family history and clinical manifestations in 58 patients]. , 2009, Medicina.
[37] A. Davis. The pathophysiology of hereditary angioedema. , 2005, Clinical immunology.
[38] P. Keith,et al. ALLERGY, ASTHMA & CLINICAL IMMUNOLOGY REVIEW Open Access , 2022 .
[39] K. Binkley. ALLERGY, ASTHMA & CLINICAL IMMUNOLOGY REVIEW Open Access Factor XII mutations, estrogen-dependent , 2022 .