Clinical Evaluation of Pediatric Patients with Hereditary Angioedema
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Published:2024
Issue:1
Volume:262
Page:23-27
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ISSN:0040-8727
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Container-title:The Tohoku Journal of Experimental Medicine
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language:en
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Short-container-title:Tohoku J. Exp. Med.
Author:
Kırmızıtaş Aydoğdu Ayşe1, Ürel Demir Gizem2
Affiliation:
1. Mersin City Training and Research Hospital Pediatric Allergy and Immunology 2. Mersin City Training and Research Hospital Pediatric Genetics
Publisher
Tohoku University Medical Press
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Reference19 articles.
1. Agostoni, A., Aygoren-Pursun, E., Binkley, K.E., Blanch, A., Bork, K., Bouillet, L., Bucher, C., Castaldo, A.J., Cicardi, M., Davis, A.E., De Carolis, C., Drouet, C., Duponchel, C., Farkas, H., Fay, K., et al. (2004) Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond. J. Allergy Clin. Immunol., 114, S51-131. 2. Blanch, A., Roche, O., Urrutia, I., Gamboa, P., Fontan, G. & Lopez-Trascasa, M. (2006) First case of homozygous C1 inhibitor deficiency. J. Allergy Clin. Immunol., 118, 1330-1335. Erratum in J. Allergy Clin. Immunol. 2007 Mar; 119 (3): 745. 3. Bork, K., Meng, G., Staubach, P. & Hardt, J. (2006) Hereditary angioedema: new findings concerning symptoms, affected organs, and course. Am. J. Med., 119, 267-274. 4. Bowen, T., Cicardi, M., Bork, K., Zuraw, B., Frank, M., Ritchie, B., Farkas, H., Varga, L., Zingale, L.C., Binkley, K., Wagner, E., Adomaitis, P., Brosz, K., Burnham, J., Warrington, R., et al. (2008) Hereditary angiodema: a current state-of-the-art review, VII: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema. Ann. Allergy Asthma Immunol., 100, S30-40. 5. Burks, A.W., Holgate, S.T., O’Hehir, R.E., Broide, D.H., Bacharier, L.B., Hershey, G.K.K., & Peebles, R.S. Jr. (2020) Middleton’s Allergy : Principles and Practice, 9th ed., Elsevier, Amsterdam.
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