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Article

Usefulness of testing for hereditary alpha tryptasemia in symptomatic patients with elevated tryptase

22 Jan 2020

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

Identifiers

PMID: 31981732
DOI: 10.1016/j.jaip.2020.01.012

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Related research

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Usefulness of testing for hereditary alpha tryptasemia in symptomatic patients with elevated tryptasePMID 31981732Read ↗

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

Resolving the genetics of human tryptases: implications for health, disease, and clinical use as a biomarkerSemantic proximity Read ↗

Hereditary Alpha Tryptasemia: Genotyping and Associated Clinical Features.Semantic proximity Read ↗

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

Hereditary alpha tryptasemia in identical twins.Semantic proximity Read ↗

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

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

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