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 kin...

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Detalles Bibliográficos
Autores principales: Säleby, Joanna, Bouzina, Habib, Ahmed, Salaheldin, Lundgren, Jakob, Rådegran, Göran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856495/
https://www.ncbi.nlm.nih.gov/pubmed/31754623
http://dx.doi.org/10.1183/23120541.00037-2019

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856495/
https://www.ncbi.nlm.nih.gov/pubmed/31754623
http://dx.doi.org/10.1183/23120541.00037-2019

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