Plasma receptor tyrosine kinase RET in pulmonary arterial hypertension diagnosis and differentiation

Background Pulmonary arterial hypertension (PAH) is a serious disease exhibiting unspecific symptoms, as a result of which diagnosis is often delayed and prognosis is poor. The underlying pathophysiology includes vasoconstriction and remodelling of small pulmonary arteries. As receptor tyrosine kina...

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Bibliographic Details
Main Authors: Joanna Säleby, Habib Bouzina, Salaheldin Ahmed, Jakob Lundgren, Göran Rådegran
Format: Article
Language:English
Published: European Respiratory Society 2019-11-01
Series:ERJ Open Research
Online Access:http://openres.ersjournals.com/content/5/4/00037-2019.full