Hereditary Alpha-Tryptasemia Latest Advances

Hereditary Alpha-Tryptasemia (HαT) as a Risk Modifier for Severe Anaphylaxis.

Journal: Immunology and allergy clinics of North America

Published: April 03, 2026

A Single-Nucleotide Polymorphism as a Surrogate Marker for Hereditary Alpha-Tryptasemia: Are We There Yet?

Journal: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology

Published: January 20, 2026

MRGPRX2-expressing mast cells are increased in the GI tract of individuals with active inflammatory bowel disease and hereditary α-tryptasemia.

Journal: medRxiv : the preprint server for health sciences

Published: January 08, 2026

Hereditary Alpha-Tryptasemia and Mastocytosis: What We Know and What We Need To Learn.

Journal: Current allergy and asthma reports

Published: October 25, 2025

MRGPRX2-expressing mast cells are increased in the GI tract of individuals with active inflammatory bowel disease and hereditary α-tryptasemia.

Journal: Frontiers in allergy

Published: October 15, 2025

Insights Into Hereditary Alpha-Tryptasemia From a Genome-Wide Association Study in Hymenoptera Venom Anaphylaxis.

Journal: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology

Published: October 15, 2025

Alpha-Tryptase Overexpression as a Modifier of Mast Cell-Mediated Reactions.

Journal: The journal of allergy and clinical immunology. In practice

Published: August 18, 2025

From mechanism to management: CEREMAST perspectives on the intersection of HαT and clonal mast cell disorders.

Journal: Frontiers in allergy

Published: July 28, 2025

Chlorhexidine-Induced Contact Anaphylaxis.

Journal: Cureus

Published: July 23, 2025

Hereditary alpha-tryptasemia - a potential cause of severe anaphylactic reactions and a modifier of mast cell diseases.

Journal: Swiss medical weekly

Published: June 01, 2025

Describing Clinical Characteristics and Treatment Course of Patients with Hereditary Alpha-tryptasemia: A Single-center Study.

Journal: Clinical reviews in allergy & immunology

Published: May 28, 2025

Hereditary α-Tryptasemia and Peripheral Blood KIT D816V Mutation in Patients with Pediatric Mastocytosis.

Journal: International journal of molecular sciences

Published: April 12, 2025

Hereditary Alpha-Tryptasemia Latest Advances

Find the Latest Research About Hereditary Alpha-Tryptasemia

Hereditary Alpha-Tryptasemia (HαT) as a Risk Modifier for Severe Anaphylaxis.

Hereditary Alpha-Tryptasemia (HαT) as a Risk Modifier for Severe Anaphylaxis.

A Single-Nucleotide Polymorphism as a Surrogate Marker for Hereditary Alpha-Tryptasemia: Are We There Yet?

A Single-Nucleotide Polymorphism as a Surrogate Marker for Hereditary Alpha-Tryptasemia: Are We There Yet?

MRGPRX2-expressing mast cells are increased in the GI tract of individuals with active inflammatory bowel disease and hereditary α-tryptasemia.

MRGPRX2-expressing mast cells are increased in the GI tract of individuals with active inflammatory bowel disease and hereditary α-tryptasemia.

Hereditary Alpha-Tryptasemia and Mastocytosis: What We Know and What We Need To Learn.

Hereditary Alpha-Tryptasemia and Mastocytosis: What We Know and What We Need To Learn.

MRGPRX2-expressing mast cells are increased in the GI tract of individuals with active inflammatory bowel disease and hereditary α-tryptasemia.

MRGPRX2-expressing mast cells are increased in the GI tract of individuals with active inflammatory bowel disease and hereditary α-tryptasemia.

Insights Into Hereditary Alpha-Tryptasemia From a Genome-Wide Association Study in Hymenoptera Venom Anaphylaxis.

Insights Into Hereditary Alpha-Tryptasemia From a Genome-Wide Association Study in Hymenoptera Venom Anaphylaxis.

Alpha-Tryptase Overexpression as a Modifier of Mast Cell-Mediated Reactions.

Alpha-Tryptase Overexpression as a Modifier of Mast Cell-Mediated Reactions.

From mechanism to management: CEREMAST perspectives on the intersection of HαT and clonal mast cell disorders.

From mechanism to management: CEREMAST perspectives on the intersection of HαT and clonal mast cell disorders.

Chlorhexidine-Induced Contact Anaphylaxis.

Chlorhexidine-Induced Contact Anaphylaxis.

Hereditary alpha-tryptasemia - a potential cause of severe anaphylactic reactions and a modifier of mast cell diseases.

Hereditary alpha-tryptasemia - a potential cause of severe anaphylactic reactions and a modifier of mast cell diseases.

Describing Clinical Characteristics and Treatment Course of Patients with Hereditary Alpha-tryptasemia: A Single-center Study.

Describing Clinical Characteristics and Treatment Course of Patients with Hereditary Alpha-tryptasemia: A Single-center Study.

Hereditary α-Tryptasemia and Peripheral Blood KIT D816V Mutation in Patients with Pediatric Mastocytosis.

Hereditary α-Tryptasemia and Peripheral Blood KIT D816V Mutation in Patients with Pediatric Mastocytosis.