Hereditary alpha-tryptasemia modifies clinical phenotypes among individuals with congenital hypermobility disorders
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Molecular Medicine
Reference13 articles.
1. Hereditary alpha tryptasemia is not associated with specific clinical phenotypes;Chollet;J. Allergy Clin. Immunol.,2021
2. Hereditary alpha tryptasemia is a valid genetic biomarker for severe mediator-related symptoms in mastocytosis;Greiner;Blood,2020
3. Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number;Lyons;Nat. Genet.,2016
4. Hereditary alpha-tryptasemia: UK prevalence and variability in disease expression;Robey;J. Allergy Clin. Immunol. Pract.,2020
5. Heritable risk for severe anaphylaxis associated with increased alpha-tryptase-encoding germline copy number at TPSAB1;Lyons;J. Allergy Clin. Immunol.,2020
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Hereditary Alpha Tryptasemia: Validation of a Single-Well Multiplex Digital Droplet PCR Assay in a Cohort of Symptomatic Patients;Clinical Chemistry;2023-12-11
2. Hereditary alpha-tryptasemia in patients with postural orthostatic tachycardia syndrome;The Journal of Allergy and Clinical Immunology: In Practice;2023-10
3. Defining hereditary alpha-tryptasemia as a risk/modifying factor for anaphylaxis: are we there yet?;European Annals of Allergy and Clinical Immunology;2023-03
4. Allergy: Mechanistic insights into new methods of prevention and therapy;Science Translational Medicine;2023-01-18
5. Hereditary alpha-tryptasemia;Current Opinion in Allergy & Clinical Immunology;2022-08-04
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