Idiopathic Nonhistaminergic Acquired Angioedema Versus Hereditary Angioedema.
暂无分享,去创建一个
[1] T. Zuberbier,et al. The EAACI/GA²LEN/EDF/WAO guideline for the definition, classification, diagnosis and management of urticaria , 2018, Allergy.
[2] I. Braenne,et al. Hereditary angioedema with a mutation in the plasminogen gene , 2018, Allergy.
[3] M. Margaglione,et al. Mutation of the angiopoietin‐1 gene (ANGPT1) associates with a new type of hereditary angioedema , 2017, The Journal of allergy and clinical immunology.
[4] J. Bernstein,et al. Current and future therapies for the treatment of histamine-induced angioedema , 2017, Expert opinion on pharmacotherapy.
[5] M. Triggiani,et al. International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency , 2016, Allergy.
[6] H. Farkas,et al. “Nuts and Bolts” of Laboratory Evaluation of Angioedema , 2016, Clinical Reviews in Allergy & Immunology.
[7] K. Bork,et al. Hereditary angioedema with normal C1‐INH with versus without specific F12 gene mutations , 2015, Allergy.
[8] M. Cicardi,et al. Presentation, diagnosis and treatment of angioedema without wheals: a retrospective analysis of a cohort of 1058 patients , 2015, Journal of internal medicine.
[9] I. Jáuregui,et al. Positive response to omalizumab in patients with acquired idiopathic nonhistaminergic angioedema. , 2015, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.
[10] A. Malbrán,et al. Epidemiology of angioedema without wheals in an allergy and immunology center. , 2015, Medicina.
[11] J. Bernstein,et al. Diagnosis and Treatment of Bradykinin-Mediated Angioedema: Outcomes from an Angioedema Expert Consensus Meeting , 2014, International Archives of Allergy and Immunology.
[12] J. Bernstein,et al. Idiopathic nonhistaminergic angioedema successfully treated with ecallantide, icatibant, and C1 esterase inhibitor replacement. , 2014, The journal of allergy and clinical immunology. In practice.
[13] A. Gompel,et al. Tranexamic acid as maintenance treatment for non‐histaminergic angioedema: analysis of efficacy and safety in 37 patients , 2014, Clinical and experimental immunology.
[14] M. Triggiani,et al. Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group , 2014, Allergy.
[15] K. Bork,et al. Antihistamine-resistant angioedema in women with negative family history: estrogens and F12 gene mutations. , 2013, The American journal of medicine.
[16] M. Cicardi,et al. Hereditary angioedema with normal C1 inhibitor function: consensus of an international expert panel. , 2012, Allergy and asthma proceedings.
[17] H. Farkas. Management of upper airway edema caused by hereditary angioedema , 2010, Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology.
[18] J. Oldenburg,et al. Mutational spectrum of the C1INH (SERPING1) gene in patients with hereditary angioedema , 2008, Cytogenetic and Genome Research.
[19] A. Kaplan. Angioedema , 2008, The World Allergy Organization journal.
[20] G. Kojda,et al. Nonallergic angioedema: role of bradykinin , 2007, Allergy.
[21] S. Cichon,et al. Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III. , 2006, American journal of human genetics.
[22] M. Cicardi,et al. Angioedema without urticaria: a large clinical survey , 2006, Canadian Medical Association Journal.
[23] K. Bork,et al. Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor. , 2006, Biochemical and biophysical research communications.
[24] K. Bork,et al. Hereditary angioedema: new findings concerning symptoms, affected organs, and course. , 2006, The American journal of medicine.
[25] M. Cicardi,et al. Bradykinin and the pathophysiology of angioedema. , 2003, International immunopharmacology.
[26] S. Choquet,et al. Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema. , 2000, The Journal of allergy and clinical immunology.
[27] M. Cicardi,et al. Idiopathic nonhistaminergic angioedema. , 1999, The American journal of medicine.