Zobrazeno 1 - 4
of 4
pro vyhledávání: '"type 2 HAE"'
Autor:
Ankur Kumar Jindal, MD, DM, Valerie Chiang, MBBS, Prabal Barman, MD, Archan Sil, MD, Sanchi Chawla, MSc, Elaine Y.L. Au, MBBS, FRCPA, Amit Rawat, MD, Philip H. Li, MD, FRCP
Publikováno v:
Journal of Allergy and Clinical Immunology: Global, Vol 3, Iss 1, Pp 100179- (2024)
Background: Hereditary angioedema (HAE) is a rare genetic disease. Patients with type II HAE have normal or elevated C1-inhibitor (C1-INH) levels but C1-INH protein is dysfunctional. C1-INH function requires careful sample handling and technical expe
Externí odkaz:
https://doaj.org/article/1b88a503c1b74753a1449c2532407aea
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Akademický článek
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Autor:
Jindal AK; Allergy Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India., Chiang V; Division of Clinical Immunology, Department of Pathology, Pokfulam, Hong Kong., Barman P; Allergy Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India., Sil A; Allergy Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India., Chawla S; Allergy Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India., Au EYL; Division of Clinical Immunology, Department of Pathology, Pokfulam, Hong Kong., Rawat A; Allergy Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India., Li PH; Division of Rheumatology and Clinical Immunology, Department of Medicine, Queen Mary Hospital, University of Hong Kong, Pokfulam, Hong Kong.
Publikováno v:
The journal of allergy and clinical immunology. Global [J Allergy Clin Immunol Glob] 2023 Oct 13; Vol. 3 (1), pp. 100179. Date of Electronic Publication: 2023 Oct 13 (Print Publication: 2024).