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Article

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

18 Jan 2021

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 33465452
DOI: 10.1016/j.anai.2021.01.016

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Hereditary alpha-tryptasemia in 101 patients with mast cell activation–related symptomatology including anaphylaxisPMID 33465452Read ↗

Hereditary Alpha-Tryptasemia: a Commonly Inherited Modifier of Anaphylaxis.Semantic proximity Read ↗

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Hereditary Alpha-Tryptasemia and Mastocytosis: What We Know and What We Need To Learn.Semantic proximity Read ↗

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Clinical impact of the TPSAB1 genotype in mast cell diseases: A REMA study in a cohort of 959 individuals.Semantic proximity Read ↗

Elevated Tryptase Level in a Child with Idiopathic Anaphylaxis: A Case of Hereditary Alpha-TryptasemiaSemantic proximity Read ↗

Appraisal of the evidence linking hereditary α-tryptasemia with mast cell disorders, hypermobility and dysautonomia.Semantic proximity Read ↗

Hereditary Alpha-Tryptasemia (HαT) as a Risk Modifier for Severe Anaphylaxis.Semantic proximity Read ↗

Usefulness of testing for hereditary alpha tryptasemia in symptomatic patients with elevated tryptaseSemantic proximity Read ↗

Incorporating Tryptase Genotyping Into the Workup and Diagnosis of Mast Cell Diseases and Reactions.Semantic proximity Read ↗

Mast cell activation in the context of elevated basal serum tryptase: genetics and presentations.Semantic proximity Read ↗

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