Abstract: Physiological levels of basal serum tryptase vary among healthy individuals, depending on the numbers of mast cells, basal secretion rate, copy numbers of the TPSAB1 gene encoding alpha tryptase, and renal function. Recently, there has been a growing debate about the normal range of tryptase because individuals with the hereditary alpha tryptasemia (HaT) trait may or may not be symptomatic, and if symptomatic, uncertainty exists as to whether this trait directly causes clinical phenotypes or aggravates certain conditions. In fact, most HaT-positive cases are regarded as asymptomatic concerning mast cell activation. To address this point, experts of the European Competence Network on Mastocytosis (ECNM) and the American Initiative ...
International audienceFirst described by Lawrence B. Schwartz in 1987 as a marker for anaphylaxis an...
International audienceFirst described by Lawrence B. Schwartz in 1987 as a marker for anaphylaxis an...
Hereditary Alpha Tryptasemia (HαT) is a genetic condition characterized by an increased number of co...
Abstract: Tryptase has proven to be a very useful and specific marker to demonstrate mast cell activ...
The present review considers the role of mast cells (MC) and tryptase levels in various pathological...
Background: Basalserum tryptase is a weil established marker in anaphylaxis and mast-cel/ related di...
Mast cell activation syndrome (MCAS) is a condition characterized by recurrent episodes of clinicall...
Mast cell activation syndrome (MCAS) is a condition characterized by recurrent episodes of clinicall...
Mast cell activation syndrome (MCAS) is a condition characterized by recurrent episodes of clinicall...
Background Tryptase is used as a biomarker to support the diagnosis of anaphylaxis and hematologic d...
Mast cell activation syndrome (MCAS) is a condition characterized by recurrent episodes of clinicall...
Mast cell activation syndrome (MCAS) is a condition characterized by recurrent episodes of clinicall...
Mast cell activation syndrome (MCAS) is a condition characterized by recurrent episodes of clinicall...
Abstract Better methods are needed to assess mastcell activation In vivo and to distinguish the acti...
International audienceFirst described by Lawrence B. Schwartz in 1987 as a marker for anaphylaxis an...
International audienceFirst described by Lawrence B. Schwartz in 1987 as a marker for anaphylaxis an...
International audienceFirst described by Lawrence B. Schwartz in 1987 as a marker for anaphylaxis an...
Hereditary Alpha Tryptasemia (HαT) is a genetic condition characterized by an increased number of co...
Abstract: Tryptase has proven to be a very useful and specific marker to demonstrate mast cell activ...
The present review considers the role of mast cells (MC) and tryptase levels in various pathological...
Background: Basalserum tryptase is a weil established marker in anaphylaxis and mast-cel/ related di...
Mast cell activation syndrome (MCAS) is a condition characterized by recurrent episodes of clinicall...
Mast cell activation syndrome (MCAS) is a condition characterized by recurrent episodes of clinicall...
Mast cell activation syndrome (MCAS) is a condition characterized by recurrent episodes of clinicall...
Background Tryptase is used as a biomarker to support the diagnosis of anaphylaxis and hematologic d...
Mast cell activation syndrome (MCAS) is a condition characterized by recurrent episodes of clinicall...
Mast cell activation syndrome (MCAS) is a condition characterized by recurrent episodes of clinicall...
Mast cell activation syndrome (MCAS) is a condition characterized by recurrent episodes of clinicall...
Abstract Better methods are needed to assess mastcell activation In vivo and to distinguish the acti...
International audienceFirst described by Lawrence B. Schwartz in 1987 as a marker for anaphylaxis an...
International audienceFirst described by Lawrence B. Schwartz in 1987 as a marker for anaphylaxis an...
International audienceFirst described by Lawrence B. Schwartz in 1987 as a marker for anaphylaxis an...
Hereditary Alpha Tryptasemia (HαT) is a genetic condition characterized by an increased number of co...