Hereditary alpha-tryptasemia in 101 patients with mast cell activation–related symptomatology including anaphylaxis-Reference-Cited by-同舟云学术

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Hereditary alpha-tryptasemia in 101 patients with mast cell activation–related symptomatology including anaphylaxis

Published:2021-06 Issue:6 Volume:126 Page:655-660
ISSN:1081-1206
Container-title:Annals of Allergy, Asthma & Immunology
language:en
Short-container-title:Annals of Allergy, Asthma & Immunology

Author:

Giannetti Matthew P.,Weller Emily,Bormans Concetta,Novak Peter,Hamilton Matthew J.,Castells Mariana

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Immunology and Allergy,Immunology

Reference19 articles.

1. Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number;Lyons;Nat Genet,2016

2. Hereditary alpha-tryptasemia: UK prevalence and variability in disease expression;Robey;J Allergy Clin Immunol Pract,2020

3. Clinical characteristics and risk profile of patients with elevated baseline serum tryptase;Fellinger;Allergol Immunopathol (Madr),2014

4. Greiner G, Sprinzl B, Górska A, et al. Hereditary alpha tryptasemia is a valid genetic biomarker for severe mediator-related symptoms in mastocytosis [e-pub ahead of print]. Blood. https://doi.org/10.1182/blood.2020006157, accessed October 1, 2020.

5. Lyons JJ, Chovanec J, O’Connell MP, et al. Heritable risk for severe anaphylaxis associated with increased α-tryptase-encoding germline copy number at TPSAB1 [e-pub ahead of print]. J Allergy Clin Immunol https://doi.org/10.1016/j.jaci.2020.06.035, accessed October 1, 2020.

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5. The clinical features of hereditary alpha-tryptasemia;Deutsches Ärzteblatt international;2024-04-19

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